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Health Care 🏢 Full Time ⭐️ Verified

Senior Clinical Research Associate

Novartis International AG
Basel
Salary Estimate
CHF 110.000 – CHF 140.000
Latest
Live Update
24 Mei 2026
Deadline
24 Mei 2027

Job Description

Join Novartis' pioneering Global Clinical Development team in Basel and shape the future of innovative therapies. As a Senior Clinical Research Associate, you'll drive excellence in clinical trials across Europe, ensuring regulatory compliance and patient safety while accelerating life-changing treatments to market. Our state-of-the-art facilities offer collaborative spaces where scientific rigor meets compassionate care, supported by comprehensive professional development and industry-leading benefits.

This hybrid role combines 60% field monitoring across European trial sites with 40% Basel-based strategy development. You'll work directly with cross-functional teams including medical affairs, regulatory affairs, and biostatistics to design and execute complex oncology trials. Novartis offers relocation assistance for international candidates and flexible working arrangements to support work-life integration.

Responsibilities

  • Execute Phase II-III clinical trials across 8-10 European sites, ensuring protocol adherence and GCP compliance
  • Lead site initiation, monitoring, and closeout activities with 95% audit readiness
  • Manage Investigator relationships and resolve complex site-specific operational issues
  • Analyze clinical data trends and contribute to risk-based monitoring strategies
  • Mentor junior CRAs and conduct site training on Novartis' eClinical platforms
  • Collaborate with regulatory teams to support FDA/EMA submissions and inspections
  • Present trial progress and risks to global stakeholders at quarterly steering committees

Qualifications

  • MSc/PhD in Life Sciences or Nursing with 5+ years of clinical research experience
  • Certified CRA (ACRP or SOCRA) with proven oncology trial monitoring background
  • Fluency in English and German; proficiency in French or Italian highly valued
  • Expertise in CTMS systems (e.g., Veeva Vault RIM) and ePRO/eCOA technologies
  • Demonstrated success in managing multinational investigator sites and regulatory interactions
  • Strong analytical skills with experience in risk-based monitoring methodologies
  • Exceptional problem-solving abilities and cross-cultural communication expertise

Required Skills

Clinical Research GCP Oncology Monitoring Veeva Vault Risk-Based Monitoring Regulatory Affairs Site Management Data Analysis CTMS ePRO Mentorship Stakeholder Communication

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