Senior Clinical Scientist - Depression

Posted 19 Days Ago
Be an Early Applicant
2 Locations
Remote or Hybrid
Senior level
Healthtech • Professional Services
The Role
Provide scientific leadership for a depression drug development program: design study protocols, define endpoints, analyze clinical data, author study documents, collaborate with cross-functional teams, and ensure regulatory and ethical compliance. Part-time freelance role based in Copenhagen.
Summary Generated by Built In

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 novel programme in depression. This is a part time freelance assignment.

We are open to flexibility on the FTE split for the right profile.

Key responsibilities

Current phase:

  • Contribute to the scientific strategy for the drug development programme.

  • Design and develop clinical study protocols and synopses.

  • Provide scientific input to study design, endpoints and development planning.

The role is expected to expand to include:

  • Interpreting and analysing clinical study data together with statisticians and physicians.

  • Writing and reviewing clinical study documentation.

  • Collaborating with Medical Affairs, Regulatory Affairs, biometrics and external researchers.

  • Presenting study results internally and externally.

  • Ensuring studies meet scientific, regulatory and ethical requirements.

Qualifications

  • Advanced degree in Life Sciences, Pharmacy, Medicine, Neuroscience or a related discipline (PhD, PharmD, MD or equivalent preferred).

  • Hands on clinical development experience in depression is a requirement for this assignment. Broader psychiatry or CNS experience alone will not meet the client's need.

  • Demonstrated experience authoring clinical study protocols and synopses in a drug development setting.

  • Senior enough to contribute independently to clinical development strategy in a small biotech environment.

  • Based in or able to commute to Copenhagen.

Skills Required

  • Advanced degree in Life Sciences, Pharmacy, Medicine, Neuroscience or related discipline
  • Hands-on clinical development experience in depression
  • Demonstrated experience authoring clinical study protocols and synopses
  • Senior-level experience able to contribute independently to clinical development strategy in a small biotech environment
  • Based in or able to commute to Copenhagen
  • Experience interpreting and analysing clinical study data with statisticians and physicians
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The Company
700 Employees
Year Founded: 1996

What We Do

TFS HealthScience is a global, mid-sized contract research organization (CRO) founded in Sweden. It partners with biotechnology and pharmaceutical companies across the full clinical development lifecycle, providing full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions. With teams and strategic partners spanning more than 50 countries, TFS supports specialized therapeutic programs and works to advance treatments and improve patient outcomes.

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