Study Coordinator
Study Coordinator
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$ 63875 - 75100
1 Vacancy
Job Description
The purpose of this position is to facilitate the conduct of oncology clinical trials including subject and data management according to federal regulations Good Clinical Practice and local and institutional policies. These responsibilities relate to the mission of the UNC / LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.
Required Qualifications Competencies And Experience
Knowledge of ICH GCP Federal Regulations and Guidelines and ability to follow established regulations procedures and protocols; strong computer skills; ability to gather data and document procedures; ability to plan work and coordinate multiple projects; customer oriented and ability to work in a team environment; ability to communicate effectively and professionally verbally and in writing. Requires study coordinator experience or experience in oncology clinical trials. Ability to work on evenings weekends and/or holidays occasionally required.
Preferred Qualifications Competencies And Experience
Previous experience with therapeutic clinical research involving and/or devices. Experience in Phase I II and III clinical research. Experience navigating medical records and data extraction. SOCRA / ACRP Certification. Previous study coordinator experience to include exposure to oncology clinical trials or directly related oncology study coordinator experience.
Work Schedule
Monday Friday 8:00AM 5:00PM
Required Experience:
Staff IC
Employment Type
Full-Time
