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How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could be w...

Regulatory Intelligence Manager Role Objectives The Regulatory Intelligence Manager is responsible for proactively gathering, maintaining, and assessing critical regulatory intelligence relevant to unlicensed (EAP, PTA, PA-NPP), clinical trial, and commercial regulatory pathways. This role ...

My client is a biotech company looking to appoint a Contract Manager (FTC until end February 2026). The opportunity will provide a lot of autonomy working alongside the CFO. The role will support purely on contract management and is high volume. Key Responsibilities: - Assist with ...

Global Regulatory Intelligence Manager - Clinical Trials/unlicensed supply management Location: Remote/Hybrid (UK-based) Job Type: Permanent, Full-time Regulatory Intelligence Manager with experience in regulatory affairs within Clinical Trials and/or unlicensed supply, required to join a glob...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with...

1 month ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by Ethypharm. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range We are recruiting a Continuous Impr...

Contribute to responses for health authority inquiries and safety-related submissions Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling Ensure SAE reconciliation between safety databases and clinical trial systems Monitor and interpret global pharmacovigilanc...

Lewisham and Greenwich NHS Trust is a research-active organisation with a proven track-record in clinical research. We are committed to developing our research portfolio and to enable this we are strengthening our research infrastructure. This role involves working cross-site at University Hospit...

Contribute to responses for health authority inquiries and safety-related submissions Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling Ensure SAE reconciliation between safety databases and clinical trial systems Monitor and interpret global pharmacovigilanc...

Join to apply for the Scientific Content Manager - Hem/Onc role at Medscape Join to apply for the Scientific Content Manager - Hem/Onc role at Medscape Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Medscape Content Manager – Hematology/Oncology ...

Contribute to responses for health authority inquiries and safety-related submissions Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling Ensure SAE reconciliation between safety databases and clinical trial systems Monitor and interpret global pharmacovigilanc...

The Clinical Site Monitor is responsible for overseeing and managing clinical trial sites to ensure compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP).This role involves regular site visits, data verification, and communication with site personnel to ensure...

LOCATION: London, UK or Dublin, Rep of Ireland, Barcelona, Spain ROLE TYPE: Hybrid Working The Associate Director, Clinical QA will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requireme...

Senior Clinical Trial Manager (via FSP) Oncology-Focused Midsized Pharma Company - Early Phase This role will focus on the Early Phase Oncology program in the UK and mainland Europe. To be considered for this position, candidates must have recent experience with early-phase oncology studies...

Oncology Diagnostics Competitive Intelligence (Remote) About Atacana Atacana Group, Inc. is a global competitive strategy and intelligence firm focused on the healthcare industry. We help our pharma & biotech clients develop winning strategies by combining human domain expertise with cutting-edge...

Main area: STEP Post-Registration Pharmacist Grade Band: 6 Contract: Permanent Hours: Full time - 37.5 hours per week (37.5 hours are scheduled over 7 days with time off scheduled in the rota, including residency service) Job ref: 213-CAY-6799778 Employer: King's College Hospital NHS Foundation T...

1 day ago Be among the first 25 applicants Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and ...

IT Project Manager Location: Europe, home-based At IQVIA, we are continuously expanding the boundaries of what’s possible in clinical development through advanced analytics, cutting-edge technology, and deep scientific expertise. Within our Research & Development Solutions (RDS) organization, we ...

The Clinical Trial Manager (CTM) operates cross-functionally with global accountability for operational deliverables of clinical studies from Final Protocol Concept Sheet to Clinical Study Report (CSR) and applicable results disclosure. The CTM provides operational expertise and cross-functional ...

A Career with Purpose Bionical Emas is a global Early Access Programs (EAP) and Clinical Trial Supply (CTS) group bringing life-changing medicines to patients around the world. Their range of services and capabilities benefit many of the world’s leading pharma and biotech companies. At Bionical E...

Job Description Excellent opportunity to join an expanding university spin out company that specialise in developing and implementing novel biomarker panels across disease diagnosis, drug development, clinical trials & personalised medicine. In this role, you will lead projects focused on leverag...

Contribute to responses for health authority inquiries and safety-related submissions - Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling - Ensure SAE reconciliation between safety databases and clinical trial systems - Monitor and interpret global pharmacovi...

Contribute to responses for health authority inquiries and safety-related submissions - Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling - Ensure SAE reconciliation between safety databases and clinical trial systems - Monitor and interpret global pharmacovi...

Contribute to responses for health authority inquiries and safety-related submissions - Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling - Ensure SAE reconciliation between safety databases and clinical trial systems - Monitor and interpret global pharmacovi...

Associate) Director, Clinical Affairs – Infectious Diseases | Global IVD Focus 📍 Remote – UK or France | Permanent Position A global diagnostics company is seeking an experienced Clinical Affairs leader to head their infectious disease clinical programme, supporting the development and global...

Our partner A leading full-service contract research organization (CRO) is seeking a Senior Biostatistician to join its team. With a global presence and a strong foundation in statistical and data management, the company supports a range of clients in pharmaceutical, biotechnology, and medic...

For over a century and five generations, this family-owned company has been dedicated to improving lives through innovative healthcare solutions, particularly in hormonal treatments for women's and men's health. Now seeking a Clinical Quality Manager (GCP), the company continues to build on ...

International Clinical Research Specialist – Cardiology Medical Device Trials Join a medical device start-up advancing next-generation cardiac technologies through breakthrough innovation and global clinical research. With a growing European trial programme, the company is hiring an Internat...

Our partner A leading full-service contract research organization (CRO) is seeking a Senior Biostatistician to join its team. With a global presence and a strong foundation in statistical and data management, the company supports a range of clients in pharmaceutical, biotechnology, and medic...

Are you ready to drive the future of Clinical Supply Chain from behind the scenes? Looking to be in the heart of a company where precision meets purpose? Proclinical is seeking a Clinical Supply Chain Manager to oversee the management and distribution of clinical trial supplies. This role invol...

About the Citrin Foundation The Citrin Foundation is a research-oriented non-profit organization committed to identifying a cure for citrin deficiency—a monogenic metabolic disorder—and supporting affected individuals throughout their lives. The Foundation’s mission is to drive scientific progr...

Director of Clinical Development - 6-month contract. The primary role involves overseeing medical aspects of clinical trials to ensure compliance with company standard operating procedures (SOPs), client directives, good clinical practices, and regulatory standards. Responsibilities include ...

Regulatory Affairs Manager Location: London (Hybrid) Are you a regulatory expert with a sharp eye for detail and a passion for facilitating access to critical medicines across the globe? An established and fast-growing healthcare organisation is seeking a Regulatory Affairs Manager to drive...

Are you eager to play a key role in the strategic growth of an established company? Are you looking for a long-term, successful partnership that supports your professional ambitions? Then this opportunity could be the perfect next step in your career! Our client is a German, medium-sized, fa...

Job Description Summary LOCATION: London, UK or Dublin, Rep of Ireland, Barcelona, Spain ROLE TYPE: Hybrid Working The Associate Director, Clinical QA will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Hea...

This position can be based at either our London, England or Dublin, Ireland locations. In this vital and influential role, the Global Head of Site Contracting has overall accountability for the site contracting process at Novartis, with a focus on optimizing cycle time and efficiency and thinkin...

Senior Project Manager- Expanded Access Programs Location: Hammersmith, London, UK / Hybrid Department: Project Management – Access Programs Job Type: Full-Time / Permanent Company: A Global Clinical Research Organisation that offer various services such as Access Programs, Clinical Trial ...