Regional Clinical Trial Management Associate

at  BeiGene

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.
Only Applicants with a valid work permit will be considered - we do not provide sponsorship for this position

General Description:

• Role will support the study team with Clinical Operations tasks, and/or assist in ensuring compliance including completeness and quality checks of the trial master file (TMF)
• Demonstrates basic clinical operations knowledge and strong organizational skills
• Implements best practices and shares lessons learned with team and other colleagues, as appropriate
• Adheres to ICH/GCP, local regulations, SOPs and contributes to the development and/or review of Clinical Operations Work Instructions and SOPs
• The Junior Associate role in Clinical Operations is an entry level position

This job description provides the broadest description of potential assigned activities. There will be specific roles and responsibilities assigned from this Job Description, according to project assignment(s). As such, responsibilities will include some of the following activities, but may not be limited to:
Clinical Operations support to study teams:

Support cross-functional clinical study teams from start-up through close-out:

• Assists in development of clinical trial documents, manuals, trackers (may support informed consent development and version tracking)
• Preparation and documentation of internal and external meetings by preparing agendas and minutes
• Maintaining clinical operations tracking tools e.g.
• enrollment

• More senior members of the associate team may mentor junior associates
• Associates with experience in specific tasks may mentor other associates with less or no experience in these task