Key Responsibilities
- 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 is highly desirable
- Strong leadership, communication and stakeholder management skills, coupled with a collaborative and results-driven mindset
- Fluency in English is essential
- German language skills are beneficial
Our employees are our greatest asset.
And to show our appreciation, we offer attractive benefits:
Benefits
- 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 programmes 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
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.
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Senior Clinical Project Manager (all genders) in Wedel Arbeitgeber: medac GmbH
Medac ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern nicht nur flexible Arbeitszeiten und die Möglichkeit bietet, bis zu 60% remote zu arbeiten, sondern auch eine Vielzahl von attraktiven Zusatzleistungen wie Urlaubsgeld und erfolgsbasierte Prämienzahlungen. Unsere Unternehmenskultur fördert die persönliche und berufliche Weiterentwicklung durch umfangreiche Fortbildungsangebote und Sprachkurse, während wir gleichzeitig ein gesundes Arbeitsumfeld mit regionaler Küche und Sportangeboten schaffen. Werden Sie Teil unseres engagierten Teams und tragen Sie aktiv zur Verbesserung der menschlichen Gesundheit bei.