Investigational Product Delivery Lead - Clinical Trials (m/f/d), 100%
- 09 June 2026
- 100%
- Permanent position
- Basel
About the job
#Lead #IP #ClinicalTrials#HandsOn #Cross-functional-coordination #TopJob #YourNewJob
Our customer, a pharmaceutical company based in the area of Basel, needs reinforcement. For a temporary employment (duration: 01.08.2026 - 31.01.2027) we are looking for a motivated employee.
Benefits
- An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
- Flexible working hours and extensive training opportunities
- A motivated multicultural team and environment
Your responsibilities
- Coordinate end to end investigational product delivery across 5-10 active clinical trials
- Act as the single coordination point between various stakeholders, Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners
- Actively engage and follow up with functions to ensure execution against timelines, quality, and regulatory requirements
- Maintain constant, structured communication with technical teams to translate clinical needs into executable technical actions, and keep all functions involved well informed and aware about changes in timelines
- Ensure consistent application of the IP process with focus on:
- Robustness
- Adherence to approved processes
- Traceability and documentation
- Continuous improvement
- Proactively identify risks, gaps, and dependencies and drive resolution through direct outreac h
- Support governance through clear reporting, visibility, and portfolio level tracking
- Lead and facilitate monthly cross functional IP coordination meetings and contribute to portfolio reviews
Requirements
- Degree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline.
- Good understanding on dietary supplement product development and manufacturing procedure from idea to product
- 3-5 years hands on experience in:
- Quality and/or Pharmaceutical Technology
- Oral Solid Dosage Forms
- Relevant regulatory frameworks (e.g. Pharmacopeia, GMP)
- Dietary supplement experience
- Solid understanding of clinical trial workflows
- Experience with CTMS, Veeva , or equivalent clinical systems
- Basic but practical project management capability
- A strong understanding of materials and chemical sciences is considered an asset.
- Process deployment, execution monitoring, and reporting
Fragen?
Für Fragen steht dir Renato Imboden gerne telefonisch unter +41 61 269 90 65 zur Verfügung.
Renato Imboden
Recruitment Business Partner
