Contract Clinical Study manager -based in the South East12 month rolling contract Large PharmaWorking on large Global Oncology phase III trialsBrief on the role.Accountable to...
Clinical Trial Manager
Multiple locations available: London, UK; Leuven, Belgium
Full-time office based, extremely competitive package
The Clinical Trial Manager performs as project lead for multiservice full service global clinical trials.
The successful candidate interacts with sponsors and manages the timeline and all project deliverables. This role coordinates all services contracted for the study. CTMs are also responsible for leading a team of CRAs and managing project coordinators.
- Bachelor's degree in a health related field;
- Advanced degree in a health related field preferred
- 5+ years Clinical Industry experience (CRO)
- 2+ years of Project management experience
- Strong leadership skills
WANT TO APPLY?For an immediate consideration please press 'apply' or alternatively contact Emanuele either via email (email@example.com) or on the phone (+44 0203 910 9516) now and get more information about the role.
Our team at SRG Clinical also cover roles in Biometrics, Medical Affairs, Clinical Operations, Medical Information, Pharmacovigilance and Regulatory affairs so do not hesitate to get in touch.
Fancy getting rewarded? We find that good people know good people. So when you recommend a friend to SRG and we place them in a contract or permanent job, you could earn a bonus of up to £1,000 of Red Letter Days vouchers as a thank you.
CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Permanent, Freelance, Contract, Full-time, Temporary, Therapeutic Area Leader, Country Clinical Operations, CCO, TAL, Line Management, Leadership, People Skills, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology, haematology, orphan diseases, nephrology, musculoskeletal, endocrinology, gastroenterology, infectious diseases, Budget, Protocol, Vendor oversight, Vendor management, Vendor meeting, Line Management, Ethics submissions, Regulatory body