Job Description
Join our global leader in innovative medicines as a Senior Clinical Research Associate at our Basel headquarters. You'll drive excellence in clinical trials, ensuring regulatory compliance while pioneering next-generation therapies. Collaborate with cross-functional teams to deliver high-quality data that transforms patient lives. Enjoy competitive compensation, cutting-edge facilities, and career growth in a science-driven environment.
Responsibilities
- Oversee clinical trial execution across multiple sites, ensuring protocol adherence and GCP compliance
- Conduct site monitoring visits, source data verification, and risk-based quality management
- Lead vendor management and clinical trial documentation (eCRFs, IBs, study reports)
- Collaborate with medical monitors and biostatisticians on protocol amendments and safety reporting
- Mentor junior CRAs and contribute to process optimization initiatives
- Represent clinical operations at internal meetings and regulatory authority interactions
Qualifications
- Master's degree in Life Sciences, Pharmacy, or related clinical field
- 5+ years of clinical research experience in pharmaceutical/biotech
- ICH-GCP certification and proven audit/inspection readiness
- Therapeutic area expertise in oncology or immunology preferred
- Advanced proficiency in eClinical systems (Medidata Rave, Veeva Vault)
- Exceptional communication skills and stakeholder management abilities
- Fluency in English; German proficiency highly valued