About Medac
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.
About Medac
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).
Your tasks
- 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
Your profile
- 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
Our offer
- 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.
We want everyone to feel included and welcome, and we treat everyone equally. We welcome all applications, regardless of age, gender, sexual identity, nationality, religion, ideology, ethnic and social background or disability. Anyone who is part of medac is part of a diverse – and therefore strong – team.
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Senior Clinical Project Manager (all genders) in Wedel Arbeitgeber: medac group
medac ist ein hervorragender Arbeitgeber, der seinen Mitarbeitenden nicht nur flexible Arbeitszeiten und die Möglichkeit für Homeoffice bietet, sondern auch eine Vielzahl an Entwicklungsmöglichkeiten durch die medac Akademie. Mit einem starken Fokus auf Teamarbeit und Diversität schafft das Unternehmen eine inklusive Arbeitsumgebung, in der jeder geschätzt wird und die Gesundheit der Mitarbeitenden gefördert wird – sei es durch Sportangebote oder gesunde Ernährung in den Betriebsrestaurants.
