Senior Clinical Scientist

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.

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) .

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.