Clinical Trial Manager Multiple locations available: London, UK; Leuven, BelgiumFull-time office based, extremely competitive packageThe Clinical Trial Manager performs as project lead for multiservice full...
Contract Clinical Study manager -based in the South East
12 month rolling contract - Large Pharma
Working on large Global Oncology phase III trials
Brief on the role.
Accountable to ensure all relevant studies follow our clients SOPs and GCP. With direction, may matrix with key Study conduct partners. Assist with maintaining relationships and monitor performance of CRO's and other vendors. With direction from Senior Clinical Staff, collaborate with Clinical Operations functional groups (Regional Monitoring, Data Management, and Operations Management) to ensure on time delivery of studies. Provide input into identifying implications of study progress upon overall timeline goals conduct plans. With oversight manage study start-up, conduct and close-out. Manage clinical trial material. Assist in the management of CRO's or other outsourcing partners as appropriate. Provide input into content and execution of investigator meetings / may present selected topics. Provide input into development of CRF. Provide input into site selection with coordinated input
My client will look at associates looking to make a move into a full CSM role
- Life Sciences degree or equivalent in education
- Experience in working on oncology on global clinical trail
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.
HOW TO APPLY?
Please contact Gary Montgomery on 07789878300 or email email@example.com if you would like to know more about this opportunity.
Clinical Study Manger | CSM | CPM| clinical Project Manager | Associate | pharma | pharmaceutical | Trials | clinical studies | pharmaceuticals | biotech | CRO| pharma |. ICH-GCP | Global| Oncology