Clinical Research Associate

3 days ago

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Exact Sciences

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Precision oncology • Genomic testing • Cancer screening • Genetic testing • Research and development

5001 - 10000

Description

• Execute, manage, and conduct projects associated with clinical study plans • Establish and maintain communication with clinical sites • Conduct oversight visits for outsourced studies • Serve as a point of contact for investigators and site staff • Ensure compliance with GCP/ICH/protocol guidelines • Conduct site qualifications and initiation visits • Communicate site management activities to the Clinical Project team

Requirements

• Bachelor’s Degree in field or Associate degree with 4 years monitoring experience • Highschool Diploma with a minimum 6 years of monitoring experience • Familiarity with Good Clinical Practice (GCP) guidelines • Experience with using electronic data capture (EDC) systems • Effective communication skills • Knowledge of monitoring plans, protocol compliance, and GCP guidelines • Authorization to work in the United States without sponsorship

Benefits

• Paid time off (including days for vacation, holidays, volunteering, and personal time) • Paid leave for parents and caregivers • Retirement savings plan • Wellness support • Health benefits including medical, prescription drug, dental, and vision coverage