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Senior Clinical Research Associate (CRA) - Basel

BioPharma Innovations
Basel
Salary Estimate
CHF 95.000 – CHF 125.000
Live Update
27 Mei 2026
Deadline
27 Mei 2027

Job Description

Are you ready to shape the future of medicine?

BioPharma Innovations is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join our dynamic team in Basel. As a global leader in pharmaceutical development, we are committed to delivering life-changing therapies to patients worldwide. We offer a competitive salary, comprehensive benefits, and a collaborative environment where your expertise will directly impact patient safety and clinical trial success.

Why join us?

  • Global Impact: Work on groundbreaking clinical trials that reach patients in over 40 countries.
  • Professional Growth: Access to world-class training, mentorship programs, and clear pathways to management.
  • Competitive Package: Attractive base salary, performance bonuses, and extensive health benefits.
  • Modern Work Environment: State-of-the-art facilities in the heart of the Swiss life sciences hub.

Responsibilities

  • Conduct comprehensive site initiation, monitoring, and close-out visits for global Phase II-IV clinical trials.
  • Ensure strict adherence to Good Clinical Practice (GCP), ICH guidelines, and study protocols.
  • Monitor site data integrity, ensuring accuracy and timeliness of source data and CRF entry.
  • Manage and resolve clinical trial issues, deviations, and safety concerns in a timely manner.
  • Foster strong relationships with principal investigators, site staff, and internal cross-functional teams.
  • Prepare accurate and timely monitoring reports and regulatory documentation.
  • Participate in internal audits and external inspections as required.

Qualifications

  • Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field.
  • Minimum of 4-6 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
  • Valid GCP certification (e.g., ECRP) is mandatory.
  • Fluency in English and German (written and verbal) is required.
  • Strong analytical skills with the ability to interpret complex clinical data.
  • Excellent communication, negotiation, and interpersonal skills.
  • Willingness to travel up to 40% of the time within the EMEA region.

Required Skills

Clinical Research GCP Site Monitoring Data Integrity Regulatory Affairs Life Sciences Basel Switzerland

Ready to Take on This Challenge?

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