You will take on these challenges.

Management and coordination of national and international clinical trials (Phase I-IV)
Planning, monitoring and implementation of studies in compliance with ICH-GCP and regulatory requirements.
Project responsibility for defined study phases including time, resource and budget planning
Coordination of internal interfaces and external service providers (e.g. CROs)
Responsibility for the Clinical Trial Supply in collaboration with global partners
Creation, maintenance and provision of essential study documents for authorities and ethics committees
Ensuring GMP/GCP-compliant documentation and process quality

Your advantages with us

Company pension scheme
Incentive program for referring new colleagues
Significant discounts with shopping benefits, e.g. on travel, electronics or cars
Attractive, performance-based compensation structures
Flexible working hours for the best work-life balance

Completed studies in natural sciences, medicine, pharmacy, biotechnology or a comparable field
Several years of professional experience in Clinical Operations/Clinical Trial Management is desirable.
Excellent knowledge of ICH-GCP guidelines and regulatory requirements
Experience in managing international studies and interdisciplinary project teams
Familiarity with clinical IT systems (e.g., CTMS, eTMF) is an advantage.
Structured, independent and solution-oriented work style
Strong communication and organizational skills

Responsibilities

Management and coordination of national and international clinical trials (Phase I-IV)
Planning, monitoring and implementation of studies in compliance with ICH-GCP and regulatory requirements.
Project responsibility for defined study phases including time, resource and budget planning
Coordination of internal interfaces and external service providers (e.g. CROs)
Responsibility for the Clinical Trial Supply in collaboration with global partners
Creation, maintenance and provision of essential study documents for authorities and ethics committees
Ensuring GMP/GCP-compliant documentation and process quality

Company pension scheme
Incentive program for referring new colleagues
Significant discounts with shopping benefits, e.g. on travel, electronics or cars
Attractive, performance-based compensation structures
Flexible working hours for the best work-life balance

Completed studies in natural sciences, medicine, pharmacy, biotechnology or a comparable field
Several years of professional experience in Clinical Operations/Clinical Trial Management is desirable.
Excellent knowledge of ICH-GCP guidelines and regulatory requirements
Experience in managing international studies and interdisciplinary project teams
Familiarity with clinical IT systems (e.g., CTMS, eTMF) is an advantage.
Structured, independent and solution-oriented work style
Strong communication and organizational skills