Senior Clinical Research Associate

The role

You will monitor and own the progress of clinical studies at investigative sites. You will ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations.

What you will do

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study
• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits

Required qualifications

• 4-year college degree or equivalent experience
• More than 3,5 years CRA experience within the CRO or pharmaceutical industry
• Oncology experience essential
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
• Fluency in English

Nice to have

• Phase I experience
• First-In-Human (FIH) experience

Before you apply

• Candidates must be legally authorized to work in the country of employment without employer sponsorship

About the company

Precision Medicine Group is a CRO that combines clinical trial designs, operational and medical experts, and biomarker and data analytics solutions. They focus on precision medicine and oncology development.