Senior Clinical Project Manager (all genders)

medac group

Wedel

Hybrid

EUR 90.000 - 130.000

Vollzeit

vor 42 Stunden
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

Flexible working hours with partial远?
30 days of annual vacation
Excellent cafeteria
Salaries and bonuses
medac academy training
Pension scheme
Counselling and elder care support
Sports and activities

Zusammenfassung

Medac in Wedel near Hamburg is seeking a Senior Clinical Project Manager to lead international phase I–III clinical studies and ensure delivery of study objectives.

You will oversee CROs and vendors, drive governance and risk management, collaborate across functions, and support regulatory submissions while maintaining ICH-GCP compliance. Fluency in English is essential; German skills are beneficial.

Qualifikationen

  • Advanced degree in Life Sciences, Pharmacy, Medicine or related field; PhD preferred.
  • Proven track record leading international phase I–III clinical studies.
  • Experience with CRO/vendor oversight, study governance and risk management.
  • Strong leadership and stakeholder management skills.
  • Fluency in English; German language skills beneficial.

Aufgaben

  • Lead planning, execution, and delivery of international phase I–III clinical studies.
  • Oversee CROs and vendors, ensuring quality, timelines, budgets, and objectives.
  • Establish governance, risk management, issue resolution, and performance oversight.
  • Collaborate with cross-functional teams on clinical, scientific, regulatory, and operational priorities.
  • Contribute to protocol development and trial execution strategies.
  • Ensure ICH-GCP compliance and inspection readiness.
  • Support regulatory interactions, submissions, and audits.
  • Foster collaboration, accountability, and continuous improvement.

Kenntnisse

Leadership
CRO Oversight
Stakeholder management
Regulatory understanding

Ausbildung

Advanced degree in Life Sciences, Pharmacy, Medicine

Jobbeschreibung

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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