Senior Clinical Research Associate

📋 Description

• Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the
• Assist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by
• May act as Feasibility Associate.
• Train site staff in all study procedures.
• Conduct periodic monitoring visits, including completion of monitoring visit report. Review at each
• Conduct source data verification and in-house review of clinical data and ensure timely resolution

🎯 Requirements

• 10+ years of CRA experience monitoring oncology and medical device clinical trials
• Previous experience working for a CRO is required
• Experience with oncology, respiratory and complex trials is required
• Gastrointestinal oncology and medical device clinical research experience, with emphasis on
• Strong knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory
• Fluent in English and local language(s)

🎁 Benefits

• Permanent full-time position
• Remote work (must be located on the West Coast)
• Being part of a fulfilling and rewarding career making a difference
• Join a diverse and inclusive team with global reach
• Continuous training and qualification development
• Opportunity to work on a diverse client portfolio