Senior Clinical Research Associate

The role

You will monitor and own the progress of clinical studies at investigative sites. You will coordinate study setup and monitoring activities and support clinical study teams with large scope trials.

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 regulations
• Coordinate activities required to set up and monitor a study
• Identify investigators and help prepare regulatory submissions
• Conduct pre-study and initiation visits
• Handle appropriately sized clinical trials
• Support clinical study teams with trials that are larger in scope
• Train and mentor junior staff members
• Interact directly with clients
• Initiate payments and participate in proposal activities

Required qualifications

• 4-year college degree or equivalent experience
• Holder of CRA certificate
• Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
• Experience monitoring clinical trials across a variety of therapeutic areas
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
• Fluency in English and the local language

Nice to have

• Additional language(s)
• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Study start up activities experience
• Understanding of financial management

About the company

Precision for Medicine combines the agility and collaboration of a specialized CRO with scientific expertise. The company values quality, accountability, and professional development.