Sciences humaines Offres d'emploi - Bâle-Ville (BS)

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Sciences humaines • bale ville bs

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Investigational Product Delivery Lead – Clinical Trials (m/f/d), 100%

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Investigational Product Delivery Lead - Clinical Trials

Elan Personal AGKaiseraugst, CH

Il y a 2 jours

Description de poste

Investigational Product Delivery Lead - Clinical Trials
For our long-standing partner, an international pharmaceutical company in Kaiseraugst, we are looking for are looking for a hands-on Investigational Product (IP) Delivery Lead to actively coordinate and drive the end-to-end delivery of investigational products across clinical trials.
The role is centered on day-to-day execution, strong cross-functional coordination, and continuous interaction with technical teams at CREAAS and all involved functions (Quality, Pharma and dietary Supplements Technology, Manufacturing, Supply Chain, Clinical Operations). The focus is not on owning functional execution, but on making things happen: aligning stakeholders, anticipating issues, ensuring adherence to process, and driving timely, compliant IP delivery.
Investigational Product Delivery Lead - Clinical Trials
Key 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 outreach
Support governance through clear reporting, visibility, and portfolio-level tracking
Lead and facilitate monthly cross-functional IP coordination meetings and contribute to portfolio reviews
You bring:
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
What This Role Is Not
Not a purely strategic or advisory role
Not a functional manufacturing or quality execution role
Not process “theory” ownership without practical deployment
If you are interested, please feel free to send your application to Mr Räfle jid6ac46eea jit0623a jiy26a