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

Description du poste

#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 Write an email +41 61 269 90 65