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

HELP

EDP Personalberatung GmbH

Beschreibung:	Investigational Product Delivery Lead - Clinical Trials (m/f/d), 100%
Stadt:	Basel, Schweiz
Firma:	EDP Personalberatung GmbH - Firma bewerten
Datum:	2026-06-08
Beschäftigung:	bis 100%
Salär:	zu verhandeln CHF - 40 Std/Woche
Arbeitsort:	Schweiz

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

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.

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

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:RobustnessAdherence to approved processesTraceability and documentationContinuous 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 TechnologyOral Solid Dosage FormsRelevant 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

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