Clinical Research Lead vacancy for our basel based client in the Pharma sector.

Your tasks:

• Lead the clinical protocol development process in collaboration with medical and cross-functional partners, including authorship of protocols and amendments.
• Provide scientific and medical input into study-related documents, processes and regulatory submissions.
• Develop strategic and operational execution plans for global clinical studies and support study feasibility.
• Coordinate cross-functional trial teams to ensure deliverables, timelines, quality standards and recruitment commitments are met.
• Oversee ongoing medical and scientific review of trial data, including safety trend analysis, signal detection and interpretation of study results.
• Support risk mitigation, vendor strategy, budget forecasting and implementation of best practices across assigned studies.

Your experience/knowledge:

• Approximately 6+ years’ experience in clinical trial development, ideally in a global study environment.
• Strong understanding of clinical trial methodology, ICH-GCP and relevant regulatory requirements.
• Proven experience in operational project management, including planning, prioritisation and problem solving.
• Ability to interpret trial-level data and contribute to clinical study reporting and publications.
• Language skills: English

Location: Basel, Switzerland
Work setting: On-site
Sector: Pharma
Start: 01/09/2026
Duration: 12+ months
Workload: 100%
Ref.Nr.: BH 24497

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland.

We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.