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DenmarkContractual TemporaryBiologists, Botanists, Zoologists and Related Professionals

Senior Clinical Scientist

TFS HealthScience | Copenhagen, Denmark | Salary not specified

Source: JobsPipe

Required Skills

communication
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Role snapshot

Work model
On-site
Language
Not specified
Experience
Not specified
Posted
Posted today
Application deadline
2026-10-16

What you'll do

About This Role TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. We are seeking a Senior Clinical Scientist / Clinical Development Consultant to support an innovative biotechnology company advancing a clinical development programme within Major Depressive Disorder (MDD). This is a flexible freelance consulting assignment with an initial contract through the end of the year and the possibility of extension. Key Responsibilities

  • Lead the development of clinical study synopses and full study protocols for upcoming MDD studies.
  • Contribute to clinical development strategy and overall programme planning.
  • Define study objectives, endpoints, eligibility criteria, and key design elements.
  • Collaborate with Clinical Operations, Biometrics, Regulatory Affairs, and senior stakeholders.
  • Provide scientific expertise to support development decisions and program advancement.

Future Responsibilities

  • Interpret and analyse clinical study data together with statisticians and physicians.
  • Support the preparation and review of clinical study reports and related documentation.
  • Present scientific findings internally and externally.
  • Ensure studies meet scientific, regulatory, and ethical requirements.

Qualifications

  • Advanced degree in Medicine, Neuroscience, Pharmacy, Life Sciences, or a related discipline.
  • Extensive hands-on experience in clinical development within depression.
  • Demonstrated experience authoring clinical study synopses and full study protocols.
  • Strong understanding of study design and endpoint selection in MDD studies.
  • Experience supporting Phase I, Phase Ib, or Phase II clinical development programmes.
  • Ability to work independently and contribute strategically within a small biotech environment.
  • Excellent communication and stakeholder management skills.

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