About us

HMNC Brain Health defines the future of depression and anxiety therapy: We develop innovative personalized therapies with the aim of shortening the duration of treatment, improving therapy outcomes and reducing the risk of relapse. The core activities of our company are the preclinical and clinical development and commercialization of innovative drugs for depression and anxiety disorders as well as laboratory tests that help to better target antidepressants on the market.

(Associate) Clinical Trial Manager (m/w/d)

Permanent employee, Full-time · München

Your mission

Oversee day-to-day clinical trial operations, including CRO and vendor oversight from study start-up to study closeout.
Manage study timelines, budgets, and resources to ensure successful completion of clinical trials.
Ensure that clinical trials are conducted in compliance with study protocols, ICH/GCP guidelines, and applicable regulatory requirements.
Manage site selection, study start-up, enrolment, monitoring, and closeout activities.
Conduct site visits and monitoring activities to ensure the quality of data collected, the safety of study participants, and compliance with the study protocol and regulatory requirements.
Provide regular updates to the Vice President Clinical Operations and cross-functional teams regarding study status, issues, and risks.
Contribute to the development of clinical trial documents, such as protocols, informed consent forms, and case report forms.
Ensure that all clinical trial documentation is complete, accurate, and maintained in accordance with the company's SOPs and applicable regulatory requirements.
Develop and maintain relationships with key stakeholders, including clinical investigators, study coordinators, and CROs/vendors.
Assist with the preparation and conduct of regulatory inspections and audits.

Your profile

Bachelor's degree in life sciences, nursing, or related field required.
2+ years of relevant experience in clinical research, preferably in the pharmaceutical or biotech industry.
Thorough understanding of ICH/GCP guidelines and applicable regulatory requirements.
Experience in managing clinical trials from study start-up to closeout preferable.
Experience in vendor and CRO management preferable.
Excellent written and verbal communication skills.
Strong organizational and project management skills.
Ability to work independently and as part of a team.
Flexibility to travel domestically and internationally, as required.

Why us?

An inspiring work environment in a young, motivated and international team with flat hierarchies.
A permanent position with a competitive salary in an early stage, growing and dynamic company based in Munich.
Multiple learning and development opportunities.
A growing benefit portfolio including a yearly career development budget.
Flexible and family-friendly working hours with the possibility of individual solutions including remote work.
Good connection to public transportation as well as a parking garage in the office building.
We value diversity - regardless of gender, nationality, ethnic and social origin, religion/belief, physical abilities, age as well as romantic orientation and identity.

Apply now

Full-Time , Permanent

Specialist

Updated at 03/06/2025

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