Clinical Contract Specialist I
Primary Responsibilities and Duties
1 Liaise with and support Divisional & Global Clinical Affairs and Legal Department attorneys with CA-related Agreements; must work well both with a team and independently under limited supervision, exercising discretion, poise, professionalism, maturing and ethical integrity
2 Facilitate the execution of necessary CDA and contract documents with potential sites and other parties and ensure compliance with Company standards and expectations.
3 Provide executed documents for TMF, Legal and other parties as applicable. Track contract status and maintain files. Manage approved templates.
4 Serve as primary contact with the law group, study teams, sites, procurement and external parties to ensure use of approved templates, and to facilitate the execution of necessary CDA and contract documents with potential sites and other parties and ensure compliance with Company standards and expectations.
5 May perform other duties as required
Education and Experience
1 Bachelor degree or higher preferred with concentration in the life sciences or other relevant technical area, such as clinical trials, regulatory affairs, or legal clinical trial contracting.
2 Prior experience with a Contract Tracking Database, or Clinical Trial Management System
3 At least 4 years work in managing research or clinical trial contracts.
4 Integrates active listening, teamwork, and a positive image in pursuit of team goals.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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