Regional Clinical Trial Management Associate

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

• Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical studies are executed per expected and specified quality standards, within timelines and budget.
• Supports the Clinical Research Associates and/or Study Start-up Specialists in country study delivery and ensures that delegated components of clinical studies are executed per expected and specified quality standards.
• Builds solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager.
• Supports the alignment of regional deliverables with overall study goals under the direction of the Regional Clinical Study Manager.
• Might participate in internal working groups, initiatives.
• Performs other tasks assigned by the line manager.

Essential Functions of the job:

Regional Trial Support & Collaboration

• Develops regional study management experience by supporting to oversee multiple aspects of clinical trial conduct including feasibility assessment, study start-up, document generation and review, tracking of samples and enrollment of study participants.
• Develops country study management experience by supporting CRAs and SSUSs with multiple aspects of clinical trial conduct including CTMS updates, ISF binder preparation, document collections, ICF customization, eTMF maintenance (document filing, reconciliation and review at site level or country level.
• Acquires solid knowledge of clinical research operations, including interpretation and implementation of regulations/ICH guidelines.
• Supports the Regional Clinical Study Manager with set up and logistics of regional team meetings (agenda, minutes, etc.).
• Supports the Country Heads with set up and logistics of country team meetings (agenda, minutes etc.).
• Establishes good collaboration with key stakeholders regionally, globally and at country level (Regional Clinical Study Manager, Regional Clinical Trial Management Associate, Global Study Management Associate, Clinical Research Associates and Study Start-up Specialists).
• As required, supports CRAs with various activities such as monitoring visit preparations, equipment management, Contract support, EC/regulatory submission preparation/tracking, TMF filing, SUSAR submission, etc.

Timelines, Planning and Execution

• Creates and maintains regional/country level SharePoint folders for the study and regional study team distribution lists.
• Sets up the countries and sites in the region in the appropriate systems e.g., eTMF, CTMS, etc. and makes sure information is kept up to date.
• Supports system access requests for the region/country and ensure these are managed appropriately across …