A company is looking for a Trial Master File (TMF) Specialist in Oncology.
Key Responsibilities
Ensure quality, maintenance, and completeness of Trial Master Files
Identify trends or quality concerns and oversee resolution of issues with the TMF Process Owner
Collaborate with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements
Required Qualifications
BA / BS with a minimum of 3 years of clinical research experience in academic and / or industry settings
Knowledge of and direct experience with Trial Master Files
Prior eTMF administration required
Strong Microsoft Office skills required
Comprehensive knowledge of Good Clinical Practice and Good Documentation Practice
Master Specialist • Raleigh, North Carolina, United States