Covance Clin Proj Admin I in Raleigh, North Carolina

Job Overview


Get ready to redefine what’s possible and discover your potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your ideas and rare point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.


2 year vocational or Associate's degree


Provide clerical support to project team (e.g., word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.). Previous experience working in the CRO, Pharma or Biotech industries.

  • Provide telephone coverage and related support duties.

  • Set up and maintain clinical investigator files and documentation.

  • Prepare investigator budget payments and tracking systems; generate tracking reports as assigned.

  • Data entry and maintenance of selected study tracking databases.

  • Prepare study-related documents and other materials for delivery to archives, at appropriate intervals.

  • Perform other administrative duties as assigned by management.

  • Ability to use computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook)

  • Strong interpersonal skills and professional demeanor

  • Strong communication skills and ability to speak, read, and write in English

Job Number 2018-22299

Job Category Clinical Operations

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.