Ref #: 31792

Employment type: Permanent - Full-Time

Location: United Kingdom

Posted: 14-Sep-2021

Description

Description:

•* Ensure regional/global clinical operations deliverables progress according to agree upon timelines and milestones as leader of the Study Management Team (SMT). This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor set activities as assigned by the GTL. Support GTL in leading related CRO country & site activities.
•* Study Management Team Leader
•* Site selection, enrolment, monitor study progress
•* Financial planning and tracking
•* Document development
•* Training and Investigator Meeting
•* Cross functional Study Management
•* Continuous Quality Focus
•* Data Cleaning
•* Participate in Global Clinical Development Initiatives as assigned.
* Can act as Subject Matter Expert.

Profile:

•* BS degree or equivalent required, preferably in Life Sciences (e.g., Biology, • Chemistry, Biochemistry, Nursing, Pharmacy)
*• Minimum of 6 years clinical trial management experience in the pharmaceutical industry or CRO
* Experience with management and supervision of CROs/vendors is preferred.
•* Clinical research operational knowledge, strong project planning/management and effective communication skills.
*• Experience and ability in coordinating global or regional teams in a virtual environment. Proven track record in successfully managing various aspects of trials from start-up to database lock.
* Monitoring experience is recommended or other relevant experience should be considered, such as data management or central monitoring.
•* Strong knowledge of standard Microsoft applications, willingness to learn new systems.
*• Experience with planning tools is an asset.
•* Willing to travel internationally up to 20% of time.

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