Pfizer cra jobs

IQVIA Biotech seeks a Senior Clinical Research Associate to conduct site monitoring for clinical trials with emerging biotech partners. The role involves managing study sites, ensuring regulatory compliance, tracking enrollment and data quality, and supporting protocol implementation...

 ...CRA II/Senior CRA - Early Phase ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are... 

Job Description Submit your CV and any additional required information after you have read this description by clicking on the application button. Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates...

Thermo Fisher Scientific seeks Clinical Research Associates to join its PPD Functional Service Provider division in the UK on a remote basis. The role involves clinical monitoring across multinational projects within a CRO environment, supporting pharmaceutical trials and research...

JOB DESCRIPTION Work Schedule Other Environmental Conditions Office Job Description 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...

CRA II/Senior CRA - Early Phase ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion... 

 ...with site personnel and stakeholders Requirements Bachelor's degree in scientific or healthcare-related discipline Extensive CRA experience with strong clinical trial process knowledge Ability to manage multiple sites and projects simultaneously Expertise in... 

Title: Senior CRA Locations: UK, Reading Country: United Kingdom Country code: GB Work arrangement: Office or Home Time type: Full time Posting start date (Workday): 2026-09-23 Requisition ID: JR158621 Description: Sr CRA At ICON Strategic Solutions... 

 ...ICON seeks a Clinical Research Associate II or Senior CRA for early-phase clinical trials across UK sites. The role involves managing study qualification, initiation, and monitoring activities while building strong relationships with investigators and ensuring protocol compliance... 

ICON is hiring a Senior Clinical Research Associate to oversee clinical trial activities at sponsor-dedicated sites across the UK. The role requires ensuring protocol adherence, regulatory compliance, and data integrity while managing site relationships and cross-functional...

Join IQVIA Biotech – Where Innovation Meets Impact At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won’t just be part of the process—you’ll be at the ...

 ...Fortrea seeks a CRA II to conduct site monitoring visits and manage clinical trial activities across UK locations. The role involves ensuring protocol compliance, data integrity, and regulatory adherence while supporting study initiation through closeout phases. Responsibilities... 

Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in the Midlands, offering an exciting chance to work on diverse studies while ensuring compliance with... 

Description We are seeking a CRA I or CRA II to support a routine post-market surveillance study within a dedicated FSP model. Key responsibilities include: Monitoring investigator sites across the North of England. Building strong relationships with investigators... 

IQVIA seeks an experienced Clinical Research Associate for oncology site management in Manchester. The role involves conducting monitoring visits, managing recruitment, ensuring regulatory compliance, and coordinating with study sites across multiple protocols. Responsibilities...

 ...Fortrea seeks a CRA I or II for a fixed-term post-market surveillance study role based in Maidenhead. The position involves monitoring investigator sites across Northern England, managing site relationships, and ensuring compliance with regulatory standards and data quality... 

 ...to join our team in the UK across a range of locations. **Competitive sign-on bonus considered for qualified candidates** The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to... 

 ...Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements. Responsibilities Participates in the... 

Thermo Fisher Scientific (PPD) seeks experienced Clinical Research Associates to support clinical trial operations across UK locations. The role involves site monitoring, protocol compliance oversight, data integrity verification, and coordination between investigative sites...

PPD, part of Thermo Fisher Scientific, seeks an Assistant Clinical Research Associate for remote work across UK locations. The role involves supporting clinical trial operations through site management, remote monitoring, document coordination, and compliance activities in ...

 ...years. As part of our global team, you’ll have the opportunity to perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead. As an Assistant Clinical Research Associate, you'll provide support with site preparedness, logistical support... 

 ...in the UK across a range of locations. The ACRA : Performs remote activities on assigned projects in liaison with the Remote CRA, On-Site CRA and study CTM. Provides support with regards to site preparedness, logistical support to the monitoring process, and... 

 ...Pfizer UK Undergraduate Programme 2027/2028 Global Site and Study Operations Undergraduate Clinical Development and Operations, Global Site and Study Operations Pfizer Research & Development Who can apply? Applicants must be completing a placement as part of a... 

 ...specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, our ambition is to end the HIV epidemic. As the pioneers in HIV innovation, we constantly... 

Your mission Engitix Therapeutics is a London-based biotechnology company unlocking the extracellular matrix (ECM) as a source of novel therapeutic targets for fibrosis and cancer. Through our unique understanding of the ECM, world-class technology, and distinctive approach...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include...

Who Are You? A Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support Phase I-IV clinical studies. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily...

Crick PACE Postdoctoral Fellowship This is a full-time, fixed-term 4-year position. About us The Francis Crick Institute is Europe’s largest biomedical research institute under one roof. Our world-class scientists and staff collaborate on vital research to help prevent...

This position is open exclusively to current Northeastern University Co-Op students. Work Period: January 2027 to June 2027. This is a full - time, 40 hours per week position with 5 days in office. About Serif Biomedicines Are you ready to help build the next generation...

The role is to be part of a small team of microbiologists, ensuring compliance of controlled environments and ensuring control of manufactured products through bioburden and VD Max testing. Support site development projects by ensuring control standards are maintained. Embrace...