1,000+ matching jobs for “Clinical Research Associate”

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Thermo Fisher Scientific

Medical Director/Sr Medical Director - Neurology(Remote U.S)

Remote, North Carolina, USA

… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA I/ II- FSP - Spain

Madrid, Madrid, Spain +1 location

… a company — you’ll join a team that invests in your future. Ready for your next challenge? Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation. You will be fully dedicated to one of our clients. As part …

Added Oct 16, 2026

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Thermo Fisher Scientific

Assoc Manager Site Payments - FSP

Remote, Bulgaria

Added Oct 16, 2026

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IQVIA Holdings

Regulatory and Start Up Specialist - Belgium

Zaventem, Belgium +2 locations

… Ethics Committee submissions Informed Consent Forms (ICFs) Investigator Pack (IP) release documentation Clinical Trial Agreements (CTAs) Support contract negotiation activities and timelines. Maintain accurate records …

Added Oct 15, 2026

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IQVIA Holdings

Regulatory and Start Up Specialist - Netherlands

Amsterdam, The Netherlands +3 locations

Added Oct 15, 2026

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IQVIA Holdings

Regulatory and Start Up Specialist with Contracts - Hungary

Budapest, Hungary

Added Oct 15, 2026

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Thermo Fisher Scientific

CRA - FSP - South Africa

Remote, South Africa

… to join the renowned PPD CRO and still gain invaluable client dedicated experience. A day in the Life: As a Clinical Research Associate, you will: Thrive in multi-national project teams and be focused on delivering exemplary levels of customer …

Added Oct 16, 2026

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Thermo Fisher Scientific

CRA I/II/ Sr CRA - FSP - UK

Remote, United Kingdom

… an attractive joining bonus in addition to the overall compensation package.** A day in the Life: As a Clinical Research Associate, you will: Thrive in multi-national project teams and be focused on delivering exemplary levels of customer …

Added Oct 16, 2026

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Amgen

Senior Manager Program Data Delivery

India - Hyderabad

Full time
Regular

… , actions, and closure. Chair program-level issue reviews and coordinate cross-functional resolutions with Clinical Operations, Biostats, Safety, Systems, and vendors. Coordinate program resources and surge support, …

Added Oct 15, 2026

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Abbott Laboratories

Senior Manager Medical Affairs

Mumbai, Maharashtra, India

… Medical Affairs Sub-Function, supervises professionals in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. • Contributes to implementation of clinical protocols, …

Added Oct 30, 2026

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Thermo Fisher Scientific

FSP Sr CRA (Level I)

Remote, Mexico

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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IQVIA Holdings

CRA2 - Multi-Sponsor Department

Manchester, United Kingdom +3 locations

… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, …

Added Oct 15, 2026

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Thermo Fisher Scientific

Sr/CRA I/II - UK (numerous locations)

Remote, United Kingdom

PPD, part of Thermo Fisher Scientific are currently hiring for experienced Clinical Research Associates across the UK Our clinical department defines, develops and delivers clinical …

Added Oct 16, 2026

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IQVIA Holdings

Sr. CRA 1 - Single Sponsor Dedicated

Reading, United Kingdom

… Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that …

Added Oct 15, 2026

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IQVIA Holdings

CRA 2 - Single Sponsor Dedicated

Reading, United Kingdom +3 locations

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that …

Added Oct 15, 2026

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IQVIA Holdings

FSP - Central Monitor in Mexico

Mexico City, Mexico

. Key Responsibilities Perform centralized monitoring activities for assigned global clinical studies (typically 4-5 studies simultaneously). Review and assess site-level and study-level risk signals …

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Sr CRA (Level I)

Remote, Mexico

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Senior CRA

Taguig City, Philippines

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA (Level I)

Sofia, Sofia-Capital, Bulgaria

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr CRA (Level I)

Remote, Romania

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Medical Director/Sr Medical Director - Neurology(Remote U.S)

Remote, North Carolina, USA

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Medical Director – Make an Impact at the Forefront of Innovation

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

The Medical Director provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labeling reconciliation documents, CTD modules, REMS, RMP and CSR).

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

What You'll Do:
Manage all medical aspects of contracted tasks across the pharmaceutical product life-cycle.

General Support:

Ensure tasks delegated to PV are properly executed. Adhere to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Follow client SOPs/directives and project-specific WPDs for assigned projects. Comply with CRG’s corporate policies and SOPs/WPDs.
Provide medical consultation to team members and answer all study-related medical questions. Communicate clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately.
Provide therapeutic training and protocol training on assigned studies, as requested.
Assist in writing (interpretation of safety and efficacy data) and/or reviewing CSR, IND/NDA reports, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc., to ensure that the medical content is accurate and complete.

Clinical Trial Support:

Monitor all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies.
Discuss all medical concerns with principal investigators and clients (e.g., interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in interpretation and decision-making regarding clinical situations as they relate to the investigational study.
Provide medical review of adverse events of special interest, serious adverse events, and clinical outcomes events reported by study sites.
Perform data review as specified in the client contract and data validation manual, including review of coding listings and/or full safety data to assess potential safety concerns.

Marketed Products Support:

Manage signal detection activities, scientifically review aggregate reports, contribute to label updates, and support dossier maintenance and risk management activities.
Medically review adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc.) as contracted.

Education and Experience Requirements:

• MD or equivalent required. Active medical licensure preferred.

Candidates should have at least one of the following:

Clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (comparable to 2 years). Ie Neurology Residency/Fellowship
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry.
Direct experience in safety/Pharmacovigilance (comparable to 2 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

For Senior Medical Director:

MD or equivalent required. Active medical licensure preferred.

Candidates should have a combination of clinical experience and industry experience as follows:

Clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (comparable to 2 years) and one of the following: Ie Neurology Residency/Fellowship
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
Direct experience in safety/Pharmacovigilance (comparable to 2 years).

Knowledge, Skills, Abilities:

Therapeutic expertise across one or more medical specialty or sub-specialties
Strong decision-making, problem solving, organizational skills and analytical skills
Excellent oral and written communication skills
Working knowledge of relevant safety databases (e.g. Medra)
Flexibility to travel domestically and internationally
Ability to work independently, analyze work with attention to detail, process and prioritize sensitive complex information
Proficiency in basic computer applications
Fluent in spoken and written English
Excellent interpersonal, influencing and team building skills
Understanding guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff within PV

Working Environment:

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.

Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.

Why join us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

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