Latest Clinical Research Associate Jobs

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing and executing global clinical development plans. The position involves leading cross-functional teams, driving regulatory submissions, and serving as a therapeutic expert in obesity and related areas. It requires collaboration with internal and external stakeholders, including regulatory authorities and advisory boards, to shape clinical strategy and ensure successful drug development.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Cardio-Renal Discovery Disease Area Lead

The Discovery Disease Area Lead for Cardiovascular-Renal Diseases at GSK will lead the identification and validation of therapeutic targets for chronic kidney disease, glomerulonephritis, and cardiovascular conditions. You will manage a cross-functional team, drive scientific excellence, and collaborate with external experts to translate human disease phenotype information into actionable therapeutic innovations.

GSK

Director, Oncology Translational Medicine Project Manager

The Director, Oncology Translational Medicine Project Manager, will lead project management for biomarker and diagnostic strategies across GSK’s global Oncology portfolio. Responsibilities include managing external alliances, regulatory submissions, and diagnostic target profiles, ensuring high-quality data and documentation support oncology asset development and approvals.

GSK Canterbury, United Kingdom £189,750 – £316,250 pa

GCP Compliance Director (EMEA Hub)

This role leads Good Clinical Practice (GCP) compliance across Novartis' EMEA clinical operations, ensuring trials meet regulatory, quality, and ethical standards. The director oversees audits, inspections, and compliance events, while developing a high-performing team and driving risk mitigation. They will partner with global clinical and quality leaders to strengthen inspection readiness and operational excellence in a hybrid working environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer-focused solutions in clinical environments. Receive full product training and work with cutting-edge laboratory equipment across a diverse customer base.

TRS Consulting Morningside, City Of Edinburgh, Edinburgh, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Perform troubleshooting, maintenance, and technical support across high-value scientific equipment. Receive full product training and work in a customer-facing role engaging with lab managers and technicians.

TRS Consulting Perth, Perth And Kinross, PH1 5TZ, United Kingdom £52,000 pa

Clinical Development Leader

Leads global clinical strategy for Roche’s toxicology and drug testing portfolio, designing and executing clinical development programs to support regulatory approval and market adoption. Acts as scientific authority in interactions with health agencies, drives real-world evidence integration, and collaborates with KOLs and cross-functional teams to advance diagnostic innovation. Focuses on generating robust clinical evidence to demonstrate safety, effectiveness, and scientific validity of diagnostic solutions.

Roche US$138,700 – US$257,500 pa

Clinical Development Leader

This role involves leading global clinical strategy for Roche’s toxicology and drug testing portfolio, including advanced diagnostic platforms like the cobas i601. The Clinical Development Lead will design and execute high-impact clinical programs, engage with regulatory authorities, integrate real-world evidence, and collaborate with key opinion leaders to drive diagnostic innovation and ensure scientific validity across global markets.

Roche

On-site Permanent

Clinical Study Start Up Lead

This role involves leading the start-up of UK clinical trials, including regulatory submissions, site activation, and contract management. You will work closely with clinical sites, internal teams, and external partners, managing complex studies across multiple therapeutic areas.

Clearline Recruitment Ltd Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £339 – £500 pd

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

Senior Clinical Trial Manager, Cambridge, MA

The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Associate Director, Clinical Program Management, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and managing timelines, budgets, and vendor partnerships. The role leverages AI and emerging technologies to drive efficient clinical development with a focus on high-probability outcomes. It involves strategic oversight of CROs and collaborators while ensuring alignment between clinical objectives and company goals.

Isomorphic Labs England

Hybrid Permanent