Clinical Trial Supply Manager vacancy for our Basel based client in the Pharma sector.

We are looking to hire talent for a global project management role in Clinical Supply Chain.
Clinical Trial Supply Manager defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.

Your tasks:

• Lead study supply planning and execution to ensure clinical trial materials are delivered on time and supply to patients is uninterrupted.
• Develop and manage end-to-end clinical supplies for a broad range of studies, including traditional clinical trials and advanced Radio Ligand and Cell & Gene Therapy studies.
• Provide input into clinical study protocols and create optimal packaging design and distribution plans using a risk-based, patient-centric approach.
• Independently manage IRT, packaging, and distribution vendors cost-effectively throughout the study lifecycle, including final closing activities.
• Utilise GMP planning systems (SAP and Rapid Response) to ensure efficient cross-functional resource and supply planning.
• Act as single point of contact (SPOC) for the Clinical Trial team, representing Global Clinical Supply at trial level.

Your experience/knowledge:

• Master’s, PhD in life sciences, or an MBA with a scientific degree, or equivalent experience in life sciences.
• Minimum 5 years of practical experience in clinical supplies within the pharmaceutical industry.
• Strong operational excellence and high attention to detail.
• Advanced project management skills and experience with at least 3 years in SAP supply chain systems for forecasting and demand planning.
• Good understanding of GMP processes and requirements is desirable.
• Language skills: English

Your soft skills:

• Strong organisation and planning abilities.
• High learning agility, especially in working with digital/data tools.
• Ability to work independently while collaborating as part of an international team.

Location: Basel, Switzerland
Work setting: On-site
Sector: Pharma
Start: ASAP
Duration: 18+ months
Workload: 100%
Ref. Nr.: BH 24266

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland.

We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.