Clinical Documentation Specialist

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.