Clinical Project Manager

Clinical Project Manager

Miejsce pracy: Wrocław

Your responsibilities

• Lead CRO and vendor contract negotiations, budget management, and oversight of external service providers.
• Coordinate protocol and substantial amendments, including preparation, submission, implementation, and related study documentation.
• Oversee clinical trial execution, timelines, milestones, and operational deliverables in compliance with GCP, SOPs, FDA, EMA, and ICH guidelines.
• Support development of study protocols, CRFs, and other study-related documentation.
• Manage routine trial activities, TMF maintenance, site report review, and operational issue resolution.
• Collaborate cross-functionally with regulatory, pharmacovigilance, data management, and external stakeholders to ensure efficient study conduct.
• Support data analysis and interpretation for decision-making and regulatory submissions.
• Ensure high standards of quality, documentation, compliance, risk management, and implementation of corrective/preventive actions where required.

Our requirements

• Minimum 10 years of experience in clinical trial operations, clinical project management, or related areas.
• Strong experience in CRO/vendor management, contract negotiations, and budget oversight.
• Proven experience managing protocol amendments and clinical trial documentation.
• In-depth knowledge of FDA, EMA, ICH-GCP, and international clinical research regulations.
• Bachelor’s or Master’s degree in life sciences, healthcare, or related field.
• Excellent organizational, communication, and stakeholder management skills.
• Fluent English, written and spoken.

What we offer

• Full-time role with remote or on-site flexibility in Wrocław, Poland.
• Opportunity to contribute to innovative clinical development programs within a growing biotech environment.
• Collaborative and science-driven R&D culture.
• Competitive compensation tailored to experience and engagement level.
• Subsidies for private healthcare, life insurance, and sports activity package.
• Access to the MyBenefit cafeteria system.
• Flexible working environment within a collaborative, innovation-driven team.
• Participation in the company stock option plan.

Benefits

• sharing the costs of sports activities
• private medical care
• sharing the costs of professional training & courses
• life insurance
• flexible working time
• fruits
• integration events
• corporate library
• coffee / tea
• charity initiatives
• Kafeteria MyBenefit
• Stock option plan

We are seeking a highly skilled and experienced Clinical Project Manager to join our dynamic R&D organization. You will play a pivotal role in creating, conducting and executing clinical programs while maintaining full compliance with international regulatory standards.

Candidates are asked to submit their applications. We retain the right to contact only selected candidates.

Captor Therapeutics S.A

Captor Therapeutics is a biopharmaceutical company pioneering Targeted Protein Degradation (TPD) to develop breakthrough therapies for oncology and autoimmune diseases. Guided by our mission to deliver first-in-class medicines and our vision of becoming a global leader in TPD, we combine cutting-edge science with integrity, collaboration, and a commitment to patient impact. At Captor, we value transparency, growth, and scientific excellence — creating a culture where innovation and people thrive.

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