Ref #: 31845

Employment type: Permanent - Full-Time

Location: United Kingdom

Posted: 12-Oct-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, enrollment, 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)
*• Required: Minimum of 8 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.
* Strong analytical skills, and simultaneously demonstrates the ability to manage ambiguity when limited information is available.
•* Effective verbal and written communication skills leading to successful team collaboration.
* Proven experience in proactive planning, risk mitigating and gaining team consensus on updated plans during the project lifecycle.
•* Willing to travel internationally up to 20% of time.

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