Clinical Documentation Specialist

Highly Competitive Salary
  1. Permanent
  2. Clinical Trial Assistant (CTA), Program Manager / Director
  3. United States
Las Vegas, USA
Posting date: 27 Jan 2021

Proclinical is currently recruiting for a Clinical Documentation Specialist with a pharmaceutical company located in Las Vegas, NV.

Job Responsibilities:

  • Serves as the technical expert in the creation and maintenance of Clinical documents like protocol, amendments, summary of change documents, ICFs. CSRs. SAE narratives. patient summaries etc.
  • Responsible for supporting Clinical Trial document control through-out the conduct of a study.
  • Coordinates the approval of documents and distribution of sponsor documents to the CRO.
  • Supports study teams around business process needs such as Investigator meetings/Kick -off meetings/vendor coordination meeting. CDA generation.
  • Safety letter tracking, Insurance procurement. DMC documentation.
  • Reference manager, Starting Point templates. CSR appendix generation. patient safety cards and printing.

Skills and Requirements:

  • Bachelor's degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences, or drug development is desirable.
  • 0-3 years' experience

If you are having difficulty in applying or if you have any questions, please contact Bri Copeland at 267-297-3280.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.