Document Control and Quality Specialist

GDIT's Military Health team is hiring a Document Control and Quality Specialist to support a Publishing and Document Control component of a military medical research and regulatory affairs, Office of Regulated Activities (ORA), United States Army Medical Research and Development Command (USAMRDC) under the DoD (Dept. of Army) located at Ft. Detrick in Frederick, Maryland.The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service, oversight, and consultation for regulatory, clinical, non-clinical, manufacturing, data management, biostatistics, product technical, safety monitoring, and medical and regulatory writing support for FDA-regulated drug, biologic, medical device, and combination products.This position is based in the Ft. Detrick and Frederick, Maryland. Must be able to go onsite 2-3 days a weekResponsibilities:

• Provide document control and archiving support for the sponsor's electronic regulatory files and essential documents, transition of paper records to electronic media, and preparation of hard copy documents for off-site storage. Document control and archiving support includes but is not limited to the following
• Create and maintain audit ready (ensure or evaluate compliance with the designated quality system and applicable regulatory requirements) sponsor's electronic regulatory files and related essential documents provided by integrated product team or working group team members
• Assist the Government in electronic capture (scanning) of regulatory documents in a qualified Government-specified electronic document management system for inclusion in the sponsor's electronic regulatory files
• Provide consultation and training to ORA personnel or other integrated product team or working group members for essential documents that need to be stored in the sponsor's electronic regulatory files
• Perform a final clinical trial close-out of the sponsor's electronic regulatory files
• Transition paper records to electronic media
• Prepare hard copy documents for off-site storage (archival) per AR 25-400, which includes physically moving boxes up to 25 pounds
• Maintain a log and track hard copy and electronic historical and current sponsor's files and clinical trial site documents
• Provide subject matter expertise and guidance to ORA personnel or other integrated project teams or working group members
• Attend meetings as required
• Collaborate with ORA personnel to remediate any issues
• Provide subject matter expertise and support for the development and implementation of in-house quality systems and procedures to support ORA compliance

Required Qualifications:

• Bachelor's degree
• 5+ years of experience in relevant roles such as document control specialist and index control specialist
• Must have advanced proficiency with MS Office Suite (especially MS Excel)
• Exceptional communicator with ability to adjust communication style to individual personalities and needs of our customers
• Must be adept in prioritizing multiple tasks in a fast-paced customer-centric environment
• Must be U.S. citizen and be able to obtain a TI (Public Trust) clearance.

WHAT GDIT CAN OFFER YOU:

• Challenging work that makes a real impact on the world around you
• Internal mobility team dedicated to helping you own your career
• 401K with company match
• Diverse, highly collaborative teams
• Professional development, education assistance, certification and training opportunities

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Work Requirements