CTMA I

Hobson Prior are currently seeking a CTMA I for a research-based biopharmaceutical company. Our client is very patient-focused, whose scientific research has benefitted hundreds of thousands of people by ensuring medications are available to those who could otherwise not afford them. This is a contract role located in Uxbridge, London.

Job Responsibilities:

• Represent as the key operational contact with external investigators and internal stakeholders.
• Evaluates scientific proposals or protocols to identify logistical, regulatory and safety elements and implications.
• Manages assigned studies by establishing strong partnerships with external investigators and collaborators.
• Proactively identifies operational challenges and in collaboration with senior team members provides and implements solutions to ensure studies remain on track.
• Forecasts, tracks and reports CO and ISR milestones, as well as verifies completeness of the study milestones prior to invoice payment.
• Maintains efficient collaboration with company's Clinical Contracts and Finance team and external investigator/study representative to ensure contracts are executed in a timely manner.
• Supports study drug planning and shipping activities with Materials & Logistics.
• Communicates and collaborates with other functional groups to ensure efficient management of study activities.
• Delivers monthly study updates to the appropriate internal stakeholders.
• Ensures all budget or drug supply modifications are appropriately approved, documented and tracked.
• Implements working processes to promote high quality, efficient, and compliant systems for Late Phase research management.
• Responsible to support and implement Clinical Operations Quality Initiatives.
• Maintains internal Clinical Operations and Medical Affairs databases and clinical study data and document repositories.
• Completes administrative duties in a timely manner as assigned.

Key Skills:

• Excellent planning, time management, organizational, and administrative skills.
• Demonstrates core values of strong team work and accountability with ability to prioritize competing timelines and deliver excellent results.
• Excellent verbal, written, interpersonal and presentation skills are required.
• Able to maintain internal/external networking and cross-functional collaboration.
• Demonstrates a high sense of urgency and commitment to excellence in the successful execution of deliverables.
• Must be able to participate in departmental or interdepartmental strategic initiative under general supervision.

Requirements:

• Typically requires a BSc in a relevant scientific discipline.
• You will have relevant clinical experience in the pharmaceutical or health care industry or equivalent.
• Good knowledge and understanding of ICH GCP, FDA and EMEA regulations and guidelines applicable to post-authorization studies.
• You must be familiar with routine medical/scientific terminology.
• Proficient with MS Word, PowerPoint, Outlook, and Excel.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.