Senior Clinical Project Manager (all genders)
medac Gesellschaft für klinische Spezialpräparate mbH sucht: Senior Clinical Project Manager (all genders) in Wedel bei Hamburg. Die Stelle ist als Vollzeit, Homeoffice möglich ausgeschrieben. veröffentlicht am 25.09.2026.
- Arbeitgeber
- medac Gesellschaft für klinische Spezialpräparate mbH
- Ort
- Wedel bei Hamburg
- Beschäftigungsart
- Vollzeit, Homeoffice möglich
- Veröffentlicht
- 25.09.2026
Aufgaben und Anforderungen: Senior Clinical Project Manager (all genders) bei medac Gesellschaft für klinische Spezialpräparate mbH
We are a strong community: with more than 2,000 employees worldwide, we are committed to improving human health. Our work is more than just a job. With a career at medac, you can make a real difference in the industry. Look into this job opportunity and become part of an exceptional workforce.
At our location in Wedel near Hamburg, we are looking for a Senior Clinical Project Manager (all genders).
Aufgaben
- Lead the planning, execution, and delivery of international phase I–III clinical studies
- Ensure successful study conduct through effective oversight of CROs and external vendors, with accountability for quality, timelines, budgets and study objectives
- Establish and drive study governance, including risk management, issue resolution and performance oversight throughout the study lifecycle
- Collaborate closely with cross-functional teams to align clinical, scientific, regulatory and operational priorities
- Contribute to protocol development, study planning and operational strategies to support efficient trial execution
- Ensure compliance with ICH-GCP, applicable regulations and internal standards while maintaining inspection readiness
- Support interactions with health authorities and contribute to regulatory submissions, inspections and audits
- Promote a culture of collaboration, accountability and continuous improvement
Profil
- Advanced degree in Life Sciences, Pharmacy, Medicine or a related scientific field; PhD preferred
- Proven track record of successfully leading international phase I–III clinical studies
- Strong expertise in CRO and vendor oversight, study governance and operational risk management
- Sound understanding of clinical trial design, protocol development and study execution
- In-depth knowledge of ICH-GCP and global clinical research regulations
- Experience with regulatory submissions, health authority interactions and inspection readiness activities highly desirable
- Strong leadership, communication and stakeholder management skills, coupled with a collaborative and results-driven mindset
- Fluency in English essential; German language skills beneficial
Wir bieten
- Your work-life balance is important to us; we offer flexible working hours with the option of working a proportion of those hours remotely, 30 annual vacation days and an excellent cafeteria.
- Attractive salaries and success-based bonuses for all medac employees.
- Individual training opportunities: Our medac academy offers a wide range of programs including leadership training, coaching essentials and language classes.
- A funded pension scheme and other social benefits.
- We care for our employees beyond the workplace and provide advice on caring for elderly relatives as well as offering counselling.
- We promote sports and activities to improve our employees' health.
Herkunft dieser Stellenanzeige
Diese Stellenanzeige wurde von stepstone übernommen und erscheint auf Stb-Jobs.com. Die ursprüngliche Ausschreibung steht unter https://www.stepstone.de/stellenangebote----20260925---14543023-inline.html.