Hobson Prior are in search for a Senior Clinical Trial Supply to join a leading biopharmaceutical organisation dedicated to the development and manufacturing of innovative biosimilar medicines. This position will be accountable for the oversight of clinical supply planning and management throughout the lifecycle of all clinical trials sponsored or indirectly supported by the organisation.

Job Responsibilities:

• You will report to and will be supervised by the VP Clinical Operations, within the Clinical and Medical Affairs department.
• Accountable to develop Investigational Medicinal Product distribution and returns drug plans and will manage clinical supply documentation to maintain Good Manufacturing Practice and Good Clinical Practice compliance, in accordance to project scope and timelines.
• Accountable for executing organizational clinical supply strategies and standards in support of clinical trials.
• You will be requested to collaborate with cross-functional individuals (e.g. Clinical Operations, Clinical Science, Regulatory, Project Management) in support of project deliverables.
• It is expected that Manager Clinical Supplies will have to travel internationally, as required by the Project related or Department activities.

Key Skills:

• Ability to work independently as well as feel comfortable in being part of a multifunctional team.
• Self-organizational, leadership and interpersonal skills are required for this role.

Requirements:

• BS degree in a science related field.
• A proven track record of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills are expected.
• Good knowledge and understanding of the International Conference of Hamonization-GMP/GCP (ICH-GMP/GCP) is a requirement for this role.
• 3-5+ years in a Clinical Supplies Function managing IMP in the Pharmaceutical Industry, or equivalent.
• Long-standing experience in all phases of clinical drug development and a thorough understanding of the overall clinical trial supply chain (ideally for biologicals/biosimilars) is required.
• Extensive knowledge of GMP, GCP, and other relevant ICH/regulatory guidelines.
• Demonstrated experience in leading and implementation of IRT and supply distribution operations and Clinical Trial Material lifecycle.
• Willingness to travel domestically and overseas, if required.

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.