Business Unit: Global Site Activation Location: Reading, UK, hybrid working 2-3 days in office Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience,
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as
We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journey? FORTREA IN LEEDS – WHERE MEDICAL BREAKTHROUGHS BEGIN At Fortrea, our world-class Clinical Research Unit in
Coaching Director Based: London (Hammersmith) - minimum 60% office based when not delivering Contract Type: Permanent About BTS BTS is a global professional services firm that creates powerful experiences to help leaders build the future of
Shape the Future of the Environment Consultant to Principal Consultant opportunities | UK Are you passionate about solving some of today’s biggest environmental and sustainability challenges? ICF is growing its Environmental Policy team and were looking for
For the past 25 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
Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents
EZRA — Confidential JOB DESCRIPTION SVP, Coaching Services Coaching Services · Full Time · Confidential At a Glance Reports to: TBD Department: Delivery Location: London, New York or Toronto Employment type: Full time Level: Senior Vice
EZRA — Confidential JOB DESCRIPTION SVP, Coaching Services Coaching Services · Full Time · Confidential At a Glance Reports to: TBD Department: Delivery Location: London, New York or Toronto Employment type: Full time Level: Senior Vice
Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents
Build Our Future Together The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology. In this role, you
Job Description Help Shape Europes Sustainable Future Looking for a career where you can make a difference while building valuable skills and experience? At ICF, youll work on some of Europes most exciting climate, biodiversity, and sustainable
General Information Job Advert Title Clinical Development Physician (Medical Director) - Oncology Location United Kingdom Function/Business Area Research Employment Class Permanent Description Clinical Development Physician (Medical Director) - Oncology About Astellas Astellas is a global life
Who were looking for We are looking for a Lead Consultant (Economist) to join ICFs growing economics function within our UK Policy Research, Evaluation and Strategy (PRES) team. ICF is one of the UKs leading public policy consultancies,
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines,
Site Start Up Specialist 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
Analyst, Quantitative Risk Analytics (London, GB) Requisition ID 36903 Office Country United Kingdom Office City London Division Risk Management Contract Type Regular Contract Length Posting End Date 23/07/2026 Purpose of Job: Analyst, Quantitative Risk Analytics (QRA)
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document
The Senior Manager, Biosamples Operations Lead will own end-to-end biosample operations across assigned studies/programs - from operational feasibility, vendor selection, and execution of biosample operations activities through analysis and data delivery. As the primary point of