clinical research associate luxembourg

Offres d'emploi : Clinical Research au Luxembourg

19 offres d'emploi

• Dernières 24h
• Derniers 7 jours
• Derniers 30 jours

Data Steward with focus on research data management

• Sauvegarder

Université du Luxembourg

• Esch-sur-Alzette

Clinical Data Manager

Luxembourg Institute of Health

• Strassen, Luxembourg

Postdoctoral fellow (Research Associate) in Federated Learning and Analysis for Health Research

• Belval, Esch-sur-Alzette
• 83 099 €/an

Data Steward with focus on research data management and reproducibility (R&D specialist)

Healthcare digital innovation specialist (m/f/d) - cdd 24 months.

Hôpitaux Robert Schuman

Senior epidemiologist (M/F)

Laboratoire National de Santé

• Dudelange, Esch-sur-Alzette

Head of Service of Virology And Serology (M/F)

Autopsy assistant (m/f), medical secretary (m/f), 2 professor positions in nursing sciences, phd in developmental psychology, data steward focusing on data hosting and compliance (r&d), scientific full-stack python developer, private equity - family office internship (start date asap), director legal and compliance.

B Medical Systems

• Hosingen, Clervaux
• 40 952 €/an

Data Steward focusing on data hosting and compliance (R&D specialist)

Recevez par email les dernières offres d'emploi au luxembourg.

Vous pouvez annuler vos alertes email à tout moment.

Entrez votre email Créer une alerte

Dernières recherches

Clinical research.

Luxembourg (Rayon de 10 km )

Recherche Filtre

Emploi recherché

Date de publication

Type de contrat.

• Contrat (11)

Temps de travail

• Temps-plein (18)
• Université du Luxembourg (11)
• Laboratoire National de Santé (4)

Clinical Research Associate Jobs in Luxembourg

Your browser does not support iframes.

Above are the results for clinical research associate Jobs . In the left column you can filter these jobs by various filters.

You can also order the job results by relevance or by date. if you cannot find a match with these job results then please save this search as an email alert in the box above and we will send you an email with any new matching jobs when we receive them..

For Employers

Salary assessor, executive compensation assessor, nonprofit comparables assessor, our process, global salary calculator, relocation assessor, geographic assessor, occupational assessor, request a quote, learn more about eri's assessor platform.

Try a Free Demo

For Job Seekers

Salary calculator, research salaries, cost of living comparison, research cost of living, get a detailed salary report.

Get Your Customized Pay Report

Why SalaryExpert

Want to learn more about our salary data.

Schedule Time to Learn More

White Papers

Webinar recordings, stay up to date on hr news, clinical research associate, 95 249 € (eur)/yr, 45,79 € (eur) /hr, 2 124 € (eur) /yr.

The average clinical research associate gross salary in Luxembourg is 95 249 € or an equivalent hourly rate of 46 €. In addition, they earn an average bonus of 2 124 €. Salary estimates based on salary survey data collected directly from employers and anonymous employees in Luxembourg. An entry level clinical research associate (1-3 years of experience) earns an average salary of 68 217 €. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of 117 538 €.

Data powered by ERI's Assessor Platform .

This page is a promotion for the Assessor Platform and is not intended for professional use.

Professionals should subscribe to ERI's Assessor Platform .

ERI's compensation data are based on salary surveys conducted and researched by ERI. Cost of labor data in the Assessor Series are based on actual housing sales data from commercially available sources, plus rental rates, gasoline prices, consumables, medical care premium costs, property taxes, effective income tax rates, etc.

103 768 € (EUR)

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 9 % over 5 years.

This chart displays the highest level of education for: Clinical Research Associate , the majority at 100% with bachelors.

Typical Field of Study: Community Organization and Advocacy

Cost of living is calculated based on accumulating the cost of food, transportation, health services, rent, utilities, taxes, and miscellaneous.

Luxembourg ( LUK-səm-burg; Luxembourgish: Lëtzebuerg [ˈlətsəbuəɕ] ; German: Luxemburg [ˈlʊksm̩bʊʁk] ; French: Luxembourg [lyksɑ̃buʁ] ), officially the Grand Duchy of Luxembourg, is a small landlocked country in Western Europe. It is bordered by Belgium to the west and north, Germany to the east, and France to the south. Its capital and most populous city, Luxembourg City, is one of the four institutional seats of the European Union (together with Brussels, Frankfurt, and Strasbourg) and the seat...

How Much Should You Be Paid?

Learn About Our Products

• Scientist Clinical Research
• Associate Clinical Research

Subscribe to ERI SalaryExpert's Emails

For the latest in HR and compensation news, subscribe to our monthly e-newsletters, blogs, and white papers. Subscribe

19 clinical-research positions in Luxembourg

Filtered by.

• clinical-research

Refine Your Search

• Research Job 4
• Scholarship 1
• Postdoctoral 3
• University of Luxembourg 16
• Institute of Photonic Sciences 3
• Computer Science 8
• Medical Sciences 5
• Economics 1
• Humanities 1
• Mathematics 1

Scientific Full-stack Python Developer

clinical research initiatives, including Horizon and IHI-funded projects, and serve as a co-host of the ELIXIR-Luxembourg node. We are looking for a scientific full stack developer to support research data

Scienteens lab team member for Physics / Sustainability (R&D specialist)

interdisciplinary research centre of the University of Luxembourg. We conduct fundamental and translational research in the field of Systems Biology and Biomedicine – in the lab, in the clinic and in silico. We focus

Up to 9 PhD-positions available within the FLIGHT fellowship program (MSCA-COFUND action)

of the FLIGHT Program, a MCSA-COFUND doctoral program explicitly focused on intersectoral research training in collaboration with Industrial or Clinical Partners. Our PhD Fellowship Program welcomes applications

2 Professor positions in Nursing Sciences

Founded in 2003, the University of Luxembourg is the only public university in the Grand Duchy of Luxembourg. It is an international research university with a distinctly multilingual and

Post-doctoral position in applications of near-infrared spectroscopy and diffuse correlation spectroscopy in critical care

. The successful candidate will be joining the Medical Optics research group led by Prof. Turgut Durduran who is looking for a postdoctoral fellow for joining our activities in carrying out clinical studies and

Postdoctoral fellow ( Research Associate) in Federated Learning and Analysis for Health Research

clinics , and health research institutes across Luxembourg, France, Germany, and Switzerland. The project aims to revolutionize healthcare by harnessing the power of data federation, standardization, and

Research and Development Specialist – Bio Medical Image Analysis

The Luxembourg Centre for Systems Biomedicine (LCSB) is an interdisciplinary research centre of the University of Luxembourg. We conduct fundamental and translational research in the field

Research support technician at Genomics platform

The Luxembourg Centre for Systems Biomedicine (LCSB) is an interdisciplinary research centre of the University of Luxembourg. We conduct fundamental and translational research in the field

Physician-Scientist in Neurology

interdisciplinary program combining clinical , experimental, and computational approaches to Parkinson’s disease research . NCER-PD is a flagship programme funded by the Luxembourg National Research Fund (FNR) set up

Research and Development Specialist – Bioinformatician

Searches related to clinical research.

• medical sciences
• clinical research coordinator
• postdoctoral
• research fellow 55261
• epidemiology
• research assistant

• Immunological Disorders
• Precision Health
• Department of Precision Health
• Covid-19 – Infectious diseases
• Research Portal
• Quality & Safety Management office (QSMO)
• Healthcare Innovation & Assessments
• Research Pathology Platform (RPP)

Clinical and epidemiological investigation centre

The CIEC supports research and health care institutions, international academia and pharmaceutical industry players, providing them with high quality clinical research and services. 

The Clinical and Epidemiological Investigation Center (CIEC), as part of the Translational Medicine Operations Hub (TMOH) , is establishing a growing reputation in clinical research. Acting as a national centre coordinating clinical research activities involving clinicians in various medical fields, CIEC is a contact partner for pharmaceutical industries interested in conducting clinical trials in Luxembourg and works very closely with the Clinical Projects Management Office (CPMO) and the Competence Centre for Methodology and Statistics (CCMS) . CIEC stands for excellence in operational support in clinical research whilst striving to ensure respect of patient rights, data privacy and offering the opportunity to access new, innovative therapeutic approaches otherwise inaccessible.

CIEC supports research and health care institutions, international academia and pharmaceutical industry players, providing them with high quality clinical research and services. CIEC coordinated more than 7000 participants included in 140 research projects, academic or pharma-led clinical trials in the last 10 years and further aims at better addressing patients’ needs and quality of life by increasing relevant and innovative clinical research in Luxembourg, including the development of clinical and translational research.

☛ Download our Corporate Kit

Projects & clinical trials

Featured team members

Scientific publications

• Levodopa-induced dyskinesia in Parkinson’s disease – 01/09/2024 Rebecca Ting Jiin Loo and 53 other authors
• Cardiovascular history and risk of idiopathic Parkinson’s disease – 08/07/2024 Shubhra Acharya and 46 other authors
• Converging peripheral blood microRNA profiles in Parkinson’s disease and progressive supranuclear palsy – 31/05/2024 Lukas Pavelka and 125 other authors
• Comprehensive blood metabolomics profiling of Parkinson’s disease reveals coordinated alterations in xanthine metabolism – 19/03/2024 Elisa Gómez De Lope and 132 other authors
• A Phone Pal to overcome social isolation in patients with psychosis-Findings from a feasibility trial – 12/01/2024 Mariana Pinto da Costa and 2 other authors
• Education as Risk Factor of Mild Cognitive Impairment – 01/01/2024 Matthias Klee and 136 other authors
• Author Correction – 18/12/2023 Sinthuja Pachchek and 45 other authors
• Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study – 23/11/2023 Sinthuja Pachchek and 130 other authors
• Vaccine effectiveness against COVID-19 hospitalisation in adults (≥ 20 years) during Omicron-dominant circulation – 23/11/2023 Angela Mc Rose and 49 other authors
• Vaccine effectiveness against COVID-19 hospitalisation in adults (≥ 20 years) during Alpha- and Delta-dominant circulation – 01/11/2023 Angela Mc Rose and 49 other authors
• Management of pharmacovigilance during the COVID-19 pandemic crisis by the safety department of an academic sponsor – 01/06/2023 Noémie Mercier and 24 other authors
• Publisher Correction – 02/09/2022 Lukas Pavelka and 46 other authors
• Age at onset as stratifier in idiopathic Parkinson’s disease – effect of ageing and polygenic risk score on clinical phenotypes – 09/08/2022 Lukas Pavelka and 49 other authors
• Interim analysis of COVID-19 vaccine effectiveness against Severe Acute Respiratory Infection due to laboratory-confirmed SARS-CoV-2 among individuals aged 30 years and older, ECDC multi-country study – second update – 14/03/2022 Nassera Aouali and 4 other authors
• Exploring the association between patient characteristics and emergency department use in Luxembourg – 01/01/2022 Valérie Moran and 10 other authors
• An open-label randomized controlled trial of the effect of lopinavir/ritonavir, lopinavir/ritonavir plus IFN-β-1a and hydroxychloroquine in hospitalized patients with COVID-19 – 01/12/2021 Florence Ader and 50 other authors
• Systematic review and network meta-analysis of the efficacy of existing treatments for patients with recurrent glioblastoma – 09/04/2021 Anna Schritz and 6 other authors
• Repurposed Antiviral Drugs for Covid-19 – Interim WHO Solidarity Trial Results – 11/02/2021 Hongchao Pan and 50 other authors
• Creation of a pandemic memory by tracing COVID-19 infections and immunity in Luxembourg (CON-VINCE) – 09/02/2024 Olena Tsurkalenko and 30 other authors
• Luxembourg Parkinson’s study -comprehensive baseline analysis of Parkinson’s disease and atypical parkinsonism – 19/12/2023 Rejko Krüger and 25 other authors
• Author Correction – 01/01/2023 Elisabeth Letellier and 30 other authors
• Association of diet quality indices with serum and metabolic biomarkers in participants of the ORISCAV-LUX-2 study – 01/01/2023 Farhad Vahid and 28 other authors
• Associations Between Wearable-Specific Indicators of Physical Activity Behaviour and Insulin Sensitivity and Glycated Haemoglobin in the General Population – 12/12/2022 Anne Backes and 29 other authors
• Precision Health – 01/09/2022 Guy Fagherazzi and 11 other authors
• The gut microbial metabolite formate exacerbates colorectal cancer progression – 01/01/2022 Elisabeth Letellier and 30 other authors
• Association between Dietary Factors and Constipation in Adults Living in Luxembourg and Taking Part in the ORISCAV-LUX 2 Survey – 28/12/2021 Maurane Rollet and 17 other authors
• Whey-and soy protein isolates added to a carrot-tomato juice alter carotenoid bioavailability in healthy adults – 31/10/2021 Torsten Bohn and 6 other authors
• The evolution and social determinants of mental health during the first wave of the COVID-19 outbreak in Luxembourg – 01/09/2021 Fabiana Ribeiro and 10 other authors
• Rapport national du cancer au Grand-Duché de Luxembourg 2020 – 01/02/2021 Institut National du Cancer and 11 other authors
• Vivre pendant et après un cancer – 01/02/2021 Marc Karim Bendiane and 5 other authors
• Recherche – 01/02/2021 Guy Berchem and 8 other authors
• Corrigendum – 12/01/2021 Sylvia Binck and 6 other authors
• Protocol for a prospective, longitudinal cohort of people with COVID-19 and their household members to study factors associated with disease severity – 23/11/2020 Guy Fagherazzi and 13 other authors
• Contributing Factors and Evolution of Impulse Control Disorder in the Luxembourg Parkinson Cohort – 12/11/2020 Sylvia Binck and 6 other authors
• Parkinson’s disease-associated alterations of the gut microbiome predict disease-relevant changes in metabolic functions – 09/06/2020 Federico Baldini and 108 other authors
• Prevalence of SARS-CoV-2 infection in the Luxembourgish population: the CON-VINCE study. – 18/05/2020 Rejko Krüger and 23 other authors
• May measurement month 2018 – 01/07/2019 Thomas Beaney and 50 other authors
• Consentement électronique – 01/07/2019 Y. Saribekyan
• Première au Luxembourg: une étude clinique de phase 1 en cancérologie menée au Centre Hospitalier de Luxembourg en collaboration avec le Luxembourg Institute of Health – 01/03/2019 L Pernot and 1 other author
• Le LIH coordonne la phase clinique d’un vaccin thérapeutique contre le VIH – 01/02/2019 Manon Gantenbein
• Insights of the Journal of Clinical Oncology and Therapeutics – 01/01/2019
• Le LIH coordonne la phase clinique d’études pédiatriques européennes – 01/10/2018
• Requirements for certification of ECRIN data centres, with explanation and elaboration of standards, Version 4.0 – 27/04/2018 Steve Canham and 13 other authors
• Vers une recherche qui améliore notre santé et change les modes de vie. Pr Laetitia Huiart – 01/03/2018 Manon Gantenbein
• The Luxembourg Parkinson’s Study – 01/01/2018 Geraldine Hipp and 25 other authors
• No influence of supplemental dietary calcium intake on the bioavailability of spinach carotenoids in humans – 14/06/2017 Torsten Bohn and 7 other authors
• Requirements for certification of ECRIN data centres, with explanation and elaboration of standards, Version 3.0 – 26/10/2015 Steve Canham and 14 other authors
• Advice on lifestyle changes (Diet, Red Wine and Physical Activity) does not affect internal carotid and middle cerebral artery blood flow velocity in patients with carotid arteriosclerosis in a randomized controlled trial – 01/07/2014 Dirk W. Droste and 9 other authors
• A daily glass of red wine and lifestyle changes do not affect arterial blood pressure and heart rate in patients with carotid arteriosclerosis after 4 and 20 weeks – 05/10/2013 Dirk W. Droste and 9 other authors
• The use of saliva for assessment of cortisol pulsatile secretion by deconvolution analysis – 01/07/2013 Claude Muller and 3 other authors
• IL1R1+ cancer-associated fibroblasts drive tumor development and immunosuppression in colorectal cancer – 17/07/2023 Elisabeth Letellier and 27 other authors
• Le métier d’infirmier dans la recherche clinique – 01/12/2019 Daniela Valoura Esteves

Related News

Revolutionising multiple sclerosis monitoring and rehabilitation through “gamification”

Making translational medicine a reality: the LCTR-Fuerschungsklinik Lëtzebuerg opens its doors

Launch of the “Precision Health” book

Driving the future of health technology

Advancing the treatment of Parkinson’s disease

A year of Predi-COVID

LIH and Luxembourg hospitals contribute to assessing the safety of potential COVID-19 treatments

Solidarity in COVID-19 times

[Article series] The experts behind Luxembourg’s Covid-19 fight

Forthcoming events

🇬🇧 🇫🇷 🇩🇪 Medical and Translational Research Day – JRMT (HIGH SCHOOLS)

16/10/2024 08:30

🇬🇧 Medical and Translational Research Day – JRMT (HEALTHCARE & RESEARCH PROFESSIONNALS)

16/10/2024 12:00

Job vacancies

• Administrative Assistant – Clinical Studies (JA/AA0824/JG/CIEC-C) Translational Medicine Operations Hub – Clinical & Epidemiological Investigation Center
• Clinical Research Nurse (JA/CRN0624/JG/CRNT) Translational Medicine Operations Hub – Clinical & Epidemiological Investigation Center

Welcome to LIH

Privacy overview.

• ICH GCP (De)
• ICH GCP (En)
• ICH GCP (Es)
• ICH GCP (Fr)
• ICH GCP (It)
• ICH GCP (Pt)
• ICH GCP (Ru)
• AUSTRALIA (NHMRC)
• JAPAN (PMDA)
• US Clinical Trials Registry
• EU Clinical Trials Registry
• Pharmaceutical Companies
• Clinical Research Labs
• Service Companies
• Clinical Research Events
• Publications
• Researchers

List of Contract Research Organizations in Luxembourg

Global contract research organizations in luxembourg.

HEMEX is a global provider of clinical research services to small and medium-sized life sciences companies in diverse therapeutic areas. By combining extensive clinical expertise, commitment to speed, and dedication to patient-centric approaches, HEM... View full profile

• Netherlands
• Switzerland
• United States

Life sciences services from SGS – optimize your development timelines to get medicines and medical devices to market quickly and safely. There is no other area of business that is more heavily regulated than the development, testing and distribution... View full profile

• Bosnia & Herzegovina
• Burkina Faso
• Congo, DR of
• Cote d'Ivoire
• Dominican Republic
• El Salvador
• Equatorial Guinea
• New Zealand
• Papua New Guinea
• Philippines
• Saint Lucia
• Saudi Arabia
• South Africa
• South Korea
• Trinidad & Tobago
• Turkmenistan
• United Kingdom

List of CROs by location

• Czech Republic
• United Arab Emirates

• English Swedish Norwegian Finnish Danish German English French Dutch

Quick facts

Apply by: 2024-11-03

Clinical Research Associate

When our values align, there's no limit to what we can achieve.  

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability. We have currently available several Clinical Research Associate II and Senior Clinical Research Associate positions in our Clinical Operations Team in the UK.

This role can be office-based in Uxbridge or decentralized in the UK.

Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out. As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home. What you’ll do

Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.

Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.

Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.

Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).

Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.

Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you On your first day we’ll expect you to have:

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.

Ability to perform all clinical monitoring activities independently.

Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.

Strong interpersonal, written, and verbal communication skills within a matrixed team.

Experience working in a self-driven capacity, with a sense of urgency and limited oversight.

A client-focused approach to work and flexible attitude with respect to assignments/new learning.

The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).

An honest and ethical work approach to promote the development of life changing treatments for patients.

Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

If you are ready to join Parexel’s Journey, please apply!

More jobs from Talent

Similar jobs.

• Montpellier

Associate Clinical Research Coordinator – Research Biofluids Management Unit

• 1133919_RR00096357
• Research, NYU Grossman School of Medicine, Perlmutter CancerCtr (S580)
• Full-Time/Regular
• NYU Grossman School of Medicine (SOM)
• Monday – Friday; 9:00AM – 5:00PM

Apply Now -->

• Research at NYU Langone Health
• Similar Jobs
• Career Mobility
• Employee Stories

ABOUT NYU LANGONE HEALTH

NYU Langone Health is a world-class, patient-centered, integrated academic medical center. Ranked as the #1 Hospital for quality and patient safety by Vizient, Inc., and with 10 clinical specialties among the top 10 in the nation according to U.S. News & World Report , NYU Langone’s culture is rooted in excellence in patient care, education, and research. NYU Langone comprises more than 320 locations throughout the New York area and in Florida, including six inpatient locations , a children’s hospital , and four emergency rooms . Also part of NYU Langone Health is the Laura and Isaac Perlmutter Cancer Center , a National Cancer Institute designated comprehensive cancer center, NYU Grossman School of Medicine , and NYU Grossman Long Island School of Medicine . For more information, go to nyulangone.org , and interact with us on LinkedIn , Glassdoor , Indeed , Facebook , Twitter , YouTube , and Instagram .

Share this job

• Share on Facebook
• Share on Twitter
• Share on Linkedin
• Share by Mail

Working at NYU Langone Health

NYU Langone Health isn’t just a healthcare system; we’re also a research hospital with a mission to advance science and improve healthcare. We offer a collaborative approach to research that spans disciplines, pairing outstanding scientists with exceptional clinical researchers. This approach sparks new ideas and discoveries that lead to innovative advances in preventing, diagnosing, and treating disease. With access to state-of-the-art technologies and facilities, our scientists and researchers have pioneered groundbreaking medical treatments used around the world.

COVID-19 Vaccine Requirement: To protect the safety of our patients, staff, and the community at large effective August 16, 2021 NYU Langone Health requires COVID-19 vaccination of all faculty, staff, voluntary attending physicians, Howard Hughes Medical Institute employees, non-compensated faculty, students, clinical or academic observers, and volunteers, unless granted an approved exemption (in New York State, only medical exemptions shall be considered). --> Salaries shown on independent jobs related websites reflect market averages and do not represent information obtained directly from NYU Langone. We invite and encourage each candidate to discuss salary/hourly specifics during the application and hiring process.

Position Summary:

We have an exciting opportunity to join our team as an Associate Clinical Research Coordinator. Reporting to the RBMU Program Manager, the incumbent will be primarily responsible for supporting the research biospecimen/ biofluid specimen processing components of clinical research studies in the most optimal fashion. Perform accurate execution of research protocols in accordance with RBMU Standard Operating Procedures, Good Clinical Practices, HIPAA and required obligations to patient/subject, Principal Investigator, research team and the sponsor. Assist with general laboratory cleanliness and organization. Maintain sufficient clinical trial kit supply inventories. Directly interface with the research team in support of the clinical trials.

Job Responsibilities:

Support collection of biofluid research specimens for clinical trials by providing clinical collection materials to study team personnel as requested.

Monitor transport and receipt of collected research biofluid samples on a daily basis.

Maintain clinical trial biospecimen collection supply inventories for multiple studies at the same time. Monitors General Laboratory supply levels and Requests additional resources from Lab Manager when needed.

Interpret study collection plans and generate sample collection source document materials. Understand the principles of all research tests performed in research clinical trials. 

Act as point of contact for designated biospecimen collections. Respond to requests for clinical collection materials in a timely manner, give/receive correct information, encourage required dialogue/follow-through. 

Centrifuge, process, prepare, ship, and/or store biological materials in accordance with sponsor protocols, institutional standard operating procedures, Environmental Health and Safety requirements, and universal Biohazard precautions.

Perform bench work as needed, perform basic specimen processing techniques under direct supervision.

Maintain clean laboratory facilities and shared bench spaces.   Work with teammates to share general laboratory responsibilities.

Record, update, edit, and maintain confidential information relating to research biospecimens onto paperwork and/or web-based forms in a neat, accurate and timely manner and ensure subsequent data collection as required.

Help to reconcile any biospecimen discrepancies in data with RDAs and RCs. Resolve queries stemming from inappropriately reported and or recorded specimen data or missing specimens. 

Maintain study specimen inventories and Perform Quality Control Analysis on specimen collection records utilizing enterprise databases for all specimens handled and distributed.

Complete necessary Biological Hazard training provided for the proper handling and collection of biological substances and the packaging and shipment of human biofluid samples.

Provide updates to study team members regarding changes to workflow or research lab-related specific needs according to protocol modifications.

Under direct supervision, collaborate with various NYU School of Medicine and Hospital personnel involved in assisting with specific aspects of each study.

Performs all responsibilities in accordance with Standard Operating Procedures, CAP accreditation, established guidelines and work instructions, and appropriate industry and Good Clinical Practices standards.

Additional responsibilities as needed including: Help in the development of SOP’s, policy changes, education sessions, and quality improvement projects.

Minimum Qualifications:

To qualify you must have a Bachelors degree, preferably in science, public health, health education or a related field OR Associates degree with equivalent experience. Computer literate with good interpersonal, writing and verbal communication skills. 1 year relevant research experience required. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision. Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure. Proficiency in using various Microsoft Office applications such as Word, Excel, Access, Power Point and Outlook. Familiar with Internet applications. Intermediate competency in medical terminology, and Good Clinical Practice (GCP) guidelines, Federal Regulation that govern the conduct of human subjects research as well as Institutional Review Board and institutional policies and procedures related to human subjects research. 

Preferred Qualifications:

Bachelors degree in life sciences preferred. Professional certification (ACRP CCRC or SOCRA CCRP). Individuals without this certification are encouraged to obtain this certification within one year of starting in the Assistant CRC role. 2 years experience in research or related experience preferred.

Qualified candidates must be able to effectively communicate with all levels of the organization.

NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you’ll feel good about devoting your time and your talents.

NYU Grossman School of Medicine is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or parental status, citizenship status, genetic information or any other factor which cannot lawfully be used as a basis for an employment decision. We require applications to be completed online. If you wish to view NYU Grossman School of Medicine’s EEO policies, please click here . Please click here to view the Federal “EEO is the law” poster or visit https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm for more information.

NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $62,400.00 – $71,656.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.

To view the Pay Transparency Notice, please click here

NYU Grossman School of Medicine is one of the nation’s top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health , the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity, diversity, and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace diversity, inclusion, and individual skills, ideas, and knowledge. For more information, go to  med.nyu.edu , and interact with us on  LinkedIn ,  Glassdoor ,  Indeed ,   Facebook ,  Twitter  and  Instagram .

Other Jobs You May Like

How our employees grow.

• Oct 2017 Sr. Research Technician
• Nov 2019 Principal Research Technician
• June 2023 Data Analyst

• JUNE 2019 Project Associate
• SEPT 2021 Research Coordinator
• MAY 2023 Sr. Research Coordinator

• FEB 2015 Program Associate
• NOV 2015 FGP Medical Secretary
• OCT 2016 Administrative Assistant
• APRIL 2021 Program Coordinator

Ivelisse M.

• JUNE 2006 Cardiothoracic Surgery Intern
• SEPTEMBER 2011 FGP Assistant (Temp), Cardiology Associates
• JANUARY 2012 FGP Assistant, Cardiology Associates
• MARCH 2014 Administrator Coordinator, Department of Surgery
• NOVEMBER 2015 Residency/Fellowship Program Coordinator, Division of Hematology and Medical Oncology
• APRIL 2017 Senior Residency/Fellowship Program Coordinator, Division of Hematology and Medical Oncology
• MARCH 2020 Division Administrator, Hematology and Medical Oncology

• JAN 14, 1998 – OCT 11, 2012 Research Coordinator SM – Psychiatry – VA, Psychiatry MHADRP – Research
• OCT 12, 2012 – AUG 8, 2015 Research Coordinator, Psychiatry – Adult ADHD Programr
• AUG 9, 2015 – PRESENT Sr. Research Coordinator, Psychiatry – Mood & Anxiety Disorders

• JUNE 2015 ParentCorps Educator
• FEB 2018 ParentCorps Manager
• OCT 2020 Associate Director ParentCorps

• OCT 2014 Associate Research Coordinator
• JUNE 2017 Research Coordinator
• FEB 2019 Sr. Research Coordinator
• AUG 2019 Program Manager

• OCT 2017 FGP Secretary I – Intake/Scheduler
• MARCH 2019 Residency/Fellowship Program Coordinator
• NOV 2021 Senior Residency/Fellowship Program Coordinator

What Our Employees Say

• Why Work With Us
• Our Organization
• Career Opportunities
• Job Seeker FAQs
• Patient Care at NYU Langone Health
• Education & Research at NYU Langone Health

Need help accessing the site?

Diversity, equity, and inclusion statement, notice of non-discrimination, aedt bias audit results.

Clinical Research Associate- West Coast

• Location: United States
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

TA Business Partner

• Icon Strategic Solutions

Send me a message

About the role.

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out.
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs.
• Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
• Verifies proper management and accountability of Investigational Product (IP).
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries.
• Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
• Participates in audit preparation and follow-up activities as needed.
• Independently performs a variety of onsite and offsite monitoring visit types.
• Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate.
• Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives.
• May serve as preceptor, providing training to less experienced clinical team members
• 2 years of experience supporting clinical trials including 2 year of on-site monitoring experience
• In-depth knowledge of the drug development process
• In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements
• Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents
• Good spoken and written communication skills; good presentation skills
• Strong interpersonal, collaboration and time management skills
• High proficiency with Microsoft Office and company collaboration applications
• Excellent skill in the utilization of applicable clinical systems
• Excellent critical thinking skills
• Excellent organizational skills
• Ability to focus on detail for extended periods of time; high attention to accuracy
• Ability to travel extensively
• Ability to establish and maintain effective working relationships with investigative site staff
• Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

ICON and you

ICON history

Career Pathways

Benefits & Rewards

Environmental, Social & Governance

Women in IT

A better career. a better world. a better you..

Day in the life

Teaser label

Content type

Publish date

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv

Ace your virtual job interview with these proven video interview tips.

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program  Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic

Read more about ICON plc's EPIC (Entry-level Professionals in CRO (Contract Research Organization)) internship program.

Similar jobs at ICON

Clinical Monitoring

Remote Working

Business Area

ICON Strategic Solutions

Job Categories

Description

As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The primary responsibilities of this position include asses

2024-113332

Expiry date

United States

2024-113330

As a (SENIOR CRA ) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Identify, select, initiate, and close-out appropriat

2024-113318

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You

2024-112028

As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

2024-113101

As a CRA II in Italy you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with one of the worlds premi

2024-112689

Browse popular job categories below or search all jobs above