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Clinical Documentation Specialist

Lexington, MA, United StatesPosted 132 months ago
ContractremoteMid-Senior Level

Job Description

Job Description:

  • QC Review of pre-study and study documents.
  • Coding of administrative and regulatory documents.
  • Verification of documentation, maintenance of document tracking system.
  • Collaborating with CTM to determine to issues in regulatory documentation.
  • Able to Creates study specific document checklists in collaboration with the CTM and medical research.
  • Must have TMF Document experience.

Minimum Requirement:

  • Minimum 2 years’ of experience required.


  • Pharma/Bio necessary.

Thanks!!

With Regards,

Kavita Kumari

Clinical Recruiter

Integrated Resources, Inc

IT REHAB CLINICAL NURSING

Inc. 5000 – 2007-2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Tel: 732-549-2030 x208

Fax: 732-549-5549

Direct: 732-549-5302

https://www.linkedin.com/in/rkavita


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Clinical Documentation Specialist at Integrated Resources INC | Renata