Clinical Trial Manager


Bavaria
Contract
€80,000 - €90,000 EUR a year
Clinical
PR/606276_1787585403
Clinical Trial Manager

About the Opportunity

An innovative clinical-stage biotechnology company is seeking an experienced Clinical Trial Manager to support the delivery of next-generation therapies and vaccines. This is an opportunity to join a highly collaborative, science-driven environment focused on advancing novel treatment approaches and improving patient outcomes worldwide.

Offering full remote working within Germany, this role is ideal for a clinical operations professional who enjoys taking ownership of outsourced studies, collaborating cross-functionally, and working within a fast-growing biotechnology environment.

Key Responsibilities

  • Oversee the day-to-day operational management of outsourced clinical trials.
  • Manage study timelines, risks, reporting activities, and project deliverables.
  • Coordinate internal and external stakeholders to ensure successful study execution.
  • Lead oversight of CROs, central laboratories, and specialist vendors.
  • Support the development and review of study documentation.
  • Establish and oversee eTMF processes and filing activities.
  • Ensure compliance with ICH-GCP and applicable regulatory requirements.
  • Contribute to operational excellence and process improvement initiatives.
  • Support site and investigator identification, selection, and oversight.

Candidate Requirements

  • 4+ years of clinical trial experience within biotech, pharmaceutical, or CRO environments.
  • Experience managing outsourced studies and external vendors.
  • Strong understanding of clinical trial conduct, ICH-GCP, and regulatory requirements.
  • Knowledge of cross-functional clinical development activities, including data management, regulatory affairs, biostatistics, and pharmacovigilance.
  • Excellent communication, stakeholder management, and organisational skills.
  • Strong problem-solving ability and proactive mindset.
  • Fluent English required.

What's on Offer?

  • Full remote working available within Germany.
  • Opportunity to work on innovative therapies and vaccine programmes.
  • Broad exposure across clinical development and clinical operations.
  • High level of autonomy and visibility within a growing biotech.
  • Collaborative and entrepreneurial culture.
  • Opportunity to make a tangible impact on the development of future medicines.

Skills & Experience

Clinical Trial Management, Clinical Operations, Clinical Research, CRO Oversight, Vendor Management, Study Start-Up, eTMF Management, ICH-GCP, Regulatory Compliance, Clinical Development, Risk Management, Site Management, Stakeholder Management, Project Management, Biotechnology, Vaccines, Novel Therapeutic Modalities, Global Clinical Trials, Cross-Functional Collaboration.

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