This position is responsible for executing projects associated with the company clinical study plans as part of the Clinical Affairs Team. Supports study managers with clinical trial activities including but not limited to filing clinical trial documentation, querying sites on discrepant data, and drafting letters and e-mails to clinical study sites. This position is responsible to coordinate with all members of the Clinical Affiars Team to successfully execute the clinical study plans of the company

• Data entry of case report forms
• Review and audit of in-house clinical study data
• Review of study files periodically for accuracy and completeness

Mandatory Skills

• Ability to organize, present, and convey problems or issues
• Experience in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - able to create and modify spreadsheets, create complex formulas, etc.); Email – preferably Outlook; and various search engines for conducting Internet searches
• Strong verbal and written communication skills
• Effective presentation skills
• Ability to interface and work effectively within team and department with changing priorities
• Analytical, problem solving and decision-making skills
• Excellent attention to detail and organizational skills

Education/Experience Requirements

• Recent college graduate or pursuing a Bachelor’s degree in the health or life sciences

Exact Sciences is an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. The Company’s affirmative action program is available to any applicant or employee for inspection upon request.