Clinical Project Manager
Banook
Job Description
Job Description
Banook is an internationally recognised provider of reliable and innovative solutions supporting clinical trials worldwide.
\nOur German subsidiary is growing, and we are looking for a Project Manager to join our Clinical Operations team.
\nAt Banook, we value teamwork, trust, and innovation — values that drive our mission to improve the quality and efficiency of clinical research across the globe.
\nThe Role
\nAs a Project Manager, you will oversee the full life cycle of clinical studies, from setup through to close-out, ensuring quality, compliance, and customer satisfaction.
\nYou will act as the main point of contact for sponsors and internal teams, coordinating stakeholders across departments and time zones.
\nThis position requires a professional who is highly organised, autonomous, and proactive, capable of managing multiple projects independently while maintaining strong communication with international colleagues.
\nKey Responsibilities
\n- \n
- Coordinate all study-related communications and ensure clear alignment among stakeholders. \n
- Lead the planning, execution, and delivery of clinical studies on time and within budget. \n
- Monitor project performance, timelines, and risks to ensure successful study outcomes. \n
- Prepare and maintain study documentation and specifications. \n
- Ensure compliance with Banook's Quality Management System (QMS) and applicable regulatory requirements. \n
- Contribute to continuous improvement initiatives and support customer and regulatory audits. \n
About You
\nYou are a motivated and detail-oriented professional who thrives in a dynamic environment. You enjoy taking ownership of your work and collaborating with international teams.
\nQualifications and Experience:
\n- \n
- Degree in Life Sciences, Biotechnology, Public Health, Pharmaceutical Sciences, or a related field. \n
- At least 3 years' experience as a Clinical Project Manager or Clinical Research Associate. \n
- Strong understanding of local and international clinical research regulations. \n
- Excellent communication skills in English (written and spoken). \n
- Proficiency in project management and data analysis tools. \n
Skills and Attributes:
\n- \n
- Strong project planning and time management abilities. \n
- Proven experience in budget management and risk assessment. \n
- Excellent problem-solving and decision-making skills. \n
- High level of ethics, integrity, and attention to detail. \n
- Effective communication and stakeholder management. \n
- Ability to work independently and demonstrate initiative. \n
What We Offer
\n- \n
- Salary package €65K–€67K \n
- Up to two days of remote work per week. \n
- Full reimbursement of public transport costs. \n
- A dynamic, multicultural, and collaborative team environment. \n
- The opportunity to contribute to meaningful work in the field of clinical research. \n