Investigational Product Delivery Lead - Clinical Trials

ph3Investigational Product Delivery Lead - Clinical Trials /h3 pFor our long-standing partner, an international pharmaceutical company in Kaiseraugst, we 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. /p pThe 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. /p h3Key Responsibilities /h3 ul liCoordinate end‑to‑end investigational product delivery across 5–10 active clinical trials /li liAct as the single coordination point between various stakeholders, Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners /li liActively engage and follow up with functions to ensure execution against timelines, quality, and regulatory requirements /li liMaintain 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 /li liEnsure consistent application of the IP process with focus on: ul liRobustness /li liAdherence to approved processes /li liTraceability and documentation /li liContinuous improvement /li /ul /li liProactively identify risks, gaps, and dependencies and drive resolution through direct outreach /li liSupport governance through clear reporting, visibility, and portfolio‑level tracking /li liLead and facilitate monthly cross‑functional IP coordination meetings and contribute to portfolio reviews /li /ul h3You bring /h3 ul liDegree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline. /li liGood understanding of dietary supplement product development and manufacturing procedures from idea to product /li li3–5 years hands‑on experience in ul liQuality and/or Pharmaceutical Technology /li liOral Solid Dosage Forms /li liRelevant regulatory frameworks (e.g. Pharmacopeia, GMP) /li liDietary supplement experience /li /ul /li liSolid understanding of clinical trial workflows /li liExperience with CTMS, Veeva, or equivalent clinical systems /li liBasic but practical project management capability /li liA strong understanding of materials and chemical sciences is considered an asset /li liProcess deployment, execution monitoring, and reporting /li /ul h3What This Role Is Not /h3 ul liNot a purely strategic or advisory role /li liNot a functional manufacturing or quality execution role /li liNot process "theory" ownership without practical deployment /li /ul pWork location: 4303 Kaiseraugst (AG). Workload: 100%. Employment start: Immediately. Employment duration: Permanent. /p pIf you are interested, please feel free to send your application to Mr Severin Räfle /p /p #J-18808-Ljbffr