Clinical Research Associate

October 10

Apply Now

Receive Emails with Similar Jobs

TFS HealthScience

WebsiteLinkedInAll Job Openings

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

501 - 1000

Description

• Vital part of the SRS/FSP team with a global pharmaceutical sponsor • Ensure quality and integrity of clinical trials from start to finish • Assist with initial and ongoing submissions to ethics committees • Manage periodic reporting to ethics committees, including safety events • Conduct onsite monitoring and periodic central monitoring to ensure trial integrity

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 UK • Proficiency in clinical trial management systems (CTMS) and eTMF platforms • Excellent written and verbal communication skills with the ability to interact effectively with site staff and sponsor representatives

Benefits

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