Clinical Project Manager overseeing clinical trials and IT-related projects in a hybrid setup. Managing budgets, coordinating IT services, and ensuring compliance in the clinical research field.
Responsibilities
Independently manage national and international clinical drug trials
Plan and execute projects and manage project timelines
Responsible for the project budget and budget control
Coordinate IT services and platforms that support clinical studies
Translate requirements from Clinical Operations into technical specifications
Ensure the efficiency of digital tools for clients and patient groups
Work closely with technical teams to troubleshoot and resolve issues
Monitor and coordinate vendor activities
Develop and implement processes and SOPs to ensure compliance
Requirements
Degree in life sciences or a related field
Professional background in industry (e.g., CRO, pharmaceutical, or biotech)
Several years of experience as a project manager in clinical research
Deep understanding of applying and implementing IT services or decentralized study elements
Experience with non-interventional studies (NIS) as well as clinical trials
Good knowledge of GCP/ICH, ISO 14155 and ISO 20916, and AMG/MDR/IVDR
High degree of personal responsibility and strong execution skills in planning and prioritizing tasks
Analytical and solution-oriented working style
Proficient in Microsoft Office applications
Strong interpersonal skills and a team player
Benefits
Competitive compensation package
Permanent employment
30 days of vacation (based on a five-day workweek)
Flexible working hours
Overtime compensation
Option to work up to three days per week from home; possibly fully remote
Company bike program
Capital-forming payments (VWL)
Additional salary benefit for health promotion
Regular company events and team-building activities
Learning and development options (e.g., Babbel app)
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