Senior Clinical Scientist, Depression Program (Freelance)

TFS HealthScience; Malmö kommun; On-site; SEK 1,321,000 - 2,032,000; Part time

Benefits offered by this job

Part-time freelance assignment

Job summary

TFS HealthScience is seeking a Senior Clinical Scientist / Clinical Development Consultant to support a biotechnology programme in depression. This is a part-time freelance assignment with flexible FTE split.

The role involves designing and developing study protocols, providing input on endpoints, and collaborating with Medical Affairs, Regulatory, biometrics and external researchers to advance the programme while ensuring regulatory and ethical compliance.

Qualifications

• Advanced degree in Life Sciences or related field; PhD/MD/PharmD preferred.
• Hands-on clinical development experience in depression is required.
• Experience authoring clinical study protocols and synopses.
• Ability to contribute independently to clinical development strategy in a small biotech setting.
• Based in or able to commute to Copenhagen.

Responsibilities

• Contribute to scientific strategy for the drug development programme.
• Design and develop clinical study protocols and synopses.
• Provide input to study design, endpoints and development planning.
• Interpret and analyze clinical study data with statisticians and physicians.
• Write and review clinical study documentation.
• Collaborate with Medical Affairs, Regulatory, biometrics, and external researchers.
• Present study results internally and externally.
• Ensure studies meet scientific, regulatory and ethical requirements.

Skills

Clinical development

Study design input

Protocol writing

Communication skills

Collaborative teamwork

Education

PhD / PharmD / MD or equivalent preferred

Job description

TFS HealthScience is seeking a Senior Clinical Scientist / Clinical Development Consultant to support a biotechnology programme in depression. This is a part-time freelance assignment with flexible FTE split.

The role involves designing and developing study protocols, providing input on endpoints, and collaborating with Medical Affairs, Regulatory, biometrics and external researchers to advance the programme while ensuring regulatory and ethical compliance.