GSL (remote-based)

Hobson Prior are searching for a GSL to join a global pharmaceutical company on a contract basis where you will work remotely. Our client's goal is to go beyond the limits of science and change lives through ground-breaking medicines.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• To lead and optimize the performance of study delivery teams ensuring GCP compliance, including provision of timely and accurate performance feedback for study team members to the appropriate manager or CRO representative.
• Accountable to lead the delivery of the clinical study from concept to final CSR and through to study closed and archived to agreed budget, time, project standards, quality and scientific standards.
• Responsible for forecasting and day-to-day management of study timelines, budget, materials and detailed study level plans and feasibility assessment.
• Contribute to preparation and delivery of study documents (e.g. Protocols/amendments, Informed Consent Form (ICF) documents detailing study delivery data management activities, etc.).
• You will implement agreed study level process and technology for Early Oncology clinical studies.
• To manage to the agreed study timelines, budget, and resource and ensure the update of appropriate systems.
• Accountable for the quality of study planning information into relevant planning systems.
• Guide the study team in the development of outsourcing specifications and vendor selection.
• May convene and lead the cross functional study team(s) for Early Oncology Clinical studies based on delivery model.
• Any other assigned duties.

Key Skills:

• Robust collaborative communications skills including the ability to engage with a diverse client base and manage through conflict.
• Proven ability in problem solving and issues management that is solution focused.

Requirements:

• Requires a bachelor's degree in related discipline, preferably in medical or biological science.
• Comprehensive knowledge of the clinical and pharmaceutical drug development process.
• Excellent knowledge of ICH-GCP principles.
• At least 5 years progressive experience in clinical research, with at least 3 years of clinical development project management experience or equivalent.
• Extensive and proven experience in driving operational delivery to timelines, cost and quality.
• Proven experience leading delivery through internal and external organisations.
• Experience and strength in working and leading in matrix teams.
• Experience in providing clear requirements for external contracts.
• Experience in selection of external providers and development/review of contracts.
• Proven oversight of external providers.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" 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.