Senior Clinical Research Associate

October 11

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TFS HealthScience

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CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting

501 - 1000

Description

• Work exclusively with a global pharmaceutical/biotech sponsor • Ensure the quality and integrity of clinical trials • Assist with submissions and regulatory reporting • Conduct onsite monitoring and maintain documentation

Requirements

• Minimum of 5 years of clinical monitoring experience within a CRO, biotech, or pharmaceutical environment • A Bachelor’s degree in a related field (Life Sciences, Nursing, etc.) • Strong understanding of ICH-GCP guidelines and regulatory requirements in the Switzerland • Proficiency in clinical trial management systems (CTMS) and eTMF platforms • Excellent written and verbal communication skills

Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth