Clinical Trials Jobs in Maidenhead
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Search results - Clinical Trials Jobs in Maidenhead
Maidenhead
Internship Program Trial Master File (TMF) TeamLocation: Maidenhead (office-based)Full-time, 12-monthStart Date: July 2025 What if you could apply your scientific knowledge and organizational skills to advancing clinical research and ensuring compliance...
pharmiweb.jobs -
Michael Page-England
As a Scientist / Senior Scientist you will be supporting a number of allocated clinical trials utilising your virology expertise to develop, validate and conduct a number of assays and related techniques.
Client Details
The business are a leading...
Maidenhead
scientific work that helps save the lives of millions of people around the world. Our Department In the UK and Ireland, our Clinical Operations Delivery Department are involved in clinical trials at all stages, from Phase I to Phase IV.
We work closely...
pharmiweb.jobs -
Evergood Associates-England
medications, adhering to strict protocols and regulatory guidelines.
• Collaborate with oncologists, nurses, and other healthcare professionals to optimize patient outcomes.
• Participate in clinical trials and research initiatives related to oncology...
Green Life Science-England
Job Description: Freelance Pediatrician – Clinical Trial Support (UK)
Position: Freelance Paediatrician
Location: United Kingdom (Remote/On-site as required)
Contract Type: Freelance
Duration: 1 Year
About the Role:
We are seeking a dedicated...
Randstad-Maidenhead
Are you an experienced Study Start Up Project Manager? Do you have experience with a sponsor company managing outsourced clinical trials within quality, timeline, and budget expectations? If so, we would love to speak with you! The successful...
randstad.com -
BioTalent-England
role in leading the strategic and operational aspects of clinical development for our gene therapy programs. This individual will oversee the design and execution of clinical trials, collaborate cross-functionally to advance our pipeline, and ensure...
Clinical Trials – Related jobs in Maidenhead:
PE Global International-England
and manage clinical trials conducted from our Japan office. Most of these studies are local post-marketing studies in Japan, primarily conducted in Japanese, but also involve collaboration with English-speaking cross-functional colleagues.
As such, The SM...
Elevate Flexible Legal Resourcing-England
including patents and trademarks, to safeguard pharmaceutical innovations.
• Drafting and negotiating contracts related to clinical trials, licensing, distribution, and collaborations between pharmaceutical companies and other entities.
• Handling legal...
Maidenhead
or designee) to ensure that Sponsor approval is received, and the scope change processed.
• Provides leadership, mentorship, and coaching in DM related clinical trial processes, department technical capabilities, and associated turnaround durations...
pharmiweb.jobs -
Tate-England
responsibilities:
Manage the collection, processing, documentation, reporting and follow-up of all adverse event reports for all products from Clinical Trials, Non-interventional Studies, Patient Oriented Program (POPs), Literature, Spontaneous Reports, and any...
Morgan Philips Group-England
Software Licenses, AI / ML, or Clinical Trials is a considerable advantage but again not essential
• Ability to successfully manage multiple projects with complex and demanding deadlines;...
TechNet IT Recruitment (Permanent)-England
in Regulatory Affairs: Proven experience in regulatory roles within the pharmaceutical, biotech, or healthcare industry, particularly with a focus on drug development, clinical trials, and regulatory submissions.
• AI & Data Knowledge: Solid understanding...
Maidenhead
responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
• Prepares and implements project plans...
pharmiweb.jobs -
Biogen-Maidenhead
aggregate reports (PSURs, DSURs, Line Listings, RMPs), responding to safety questions from internal and external stakeholders, reviewing medical and scientific literature for safety information, and supporting Clinical Trial PV medical activities.
You...
smartrecruiters.com -
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