Investigational Product Delivery Lead

Opportunity Overview

We are seeking a highly skilled professional to lead the delivery of investigational products for our esteemed client in Kaiseraugst. This role requires a proactive individual with a strong foundation in pharmaceutical sciences and excellent coordination abilities.

Key Responsibilities

• Coordinate end-to-end investigational product delivery across 5–10 active clinical trials.
• Act as the single point of coordination between various stakeholders, including Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners.
• Engage actively and follow up with functions to ensure execution adheres to timelines, quality, and regulatory requirements.
• Maintain constant, structured communication with technical teams to translate clinical needs into executable technical actions, while keeping all functions informed of any changes in timelines.
• Ensure consistent application of the investigational product process with a focus on robustness, adherence to approved processes, traceability, documentation, and continuous improvement.
• Identify risks, gaps, and dependencies proactively, driving resolution through direct outreach.
• Support governance through clear reporting, visibility, and portfolio-level tracking.
• Lead and facilitate monthly cross-functional investigational product coordination meetings and contribute to portfolio reviews.

Qualifications

• Degree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline.
• Good understanding of dietary supplement product development and manufacturing processes from concept to product.
• 3–5 years of hands-on experience in Quality and/or Pharmaceutical Technology, including Oral Solid Dosage Forms and relevant regulatory frameworks (e.g., Pharmacopeia, GMP), with dietary supplement experience being advantageous.
• Solid understanding of clinical trial workflows.
• Experience with CTMS, Veeva, or equivalent clinical systems.
• Basic but practical project management capabilities.
• A strong understanding of materials and chemical sciences is considered an asset.
• Competence in process deployment, execution monitoring, and reporting.