Protocol Development Associate
Position Type: Permanent Staff
Department: LCCC - Clinical Trials - 426806
Appointment Type: EHRA Non-Faculty
Vacancy ID: NF0003000
Position Summary: This position will collaborate in writing, editing, producing and reviewing oncology clinical trials LOIs (letters of intent) and protocols. Priority of work is primarily self-directed with input and guidance from senior MD faculty in the clinical research program, and immediate supervisor.
Education Requirements: Advanced clinical health science degree (i.e., Pharm.D. (preferred), MSN, NP, MD) or PhD.
Qualification and Experience: Possess excellent written and oral communication skills, interpersonal skills, and be comfortable interacting with individuals at all levels internal and external to UNC Lineberger. Have a strong record of experience in clinical study design, protocol development, and working knowledge of the following: federal and local regulations of clinical trials; drug development within the pharmaceutical industry; and bio statistics. Experience and expertise in oncology research is highly desirable; candidate must enjoy working collaboratively with multidisciplinary groups of colleagues. Must be able to manage multiple projects at various stages, and be able to work independently with occasional guidance from physician leadership or management.
Equal Opportunity Employer: The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, sexual orientation, or status as a protected veteran.
Department Contact Name and Title: Kelly Kavit, HR Consultant
Department Contact Telephone Number or Email: (919) 445-4228
Special Instructions for Applicants: