Clinical Document Management Specialist

Job description

Reporting to the Clinical Documentation Team Lead, and working in collaboration with the clinical study teams, the Clinical Document Management Specialist (CDMS) is responsible for the management and oversight of Trial Master File (TMF) records from set-up through to final archival of the clinical trial, ensuring compliance with company SOPs and processes, and all applicable regulations. Focusing on inspection readiness, monitors compliance of the TMF and supports preparation of documentation required for regulatory agency inspections and internal audits. Oversees set-up and consolidation of outsourced elements of the TMF with preferred CRO vendors. With support from the management team, performs periodic quality assessments of clinical TMF documents where required. Contributes to assigned Clinical Document Management (CDM) initiatives. Responsibilities Key contributor and member of the clinical study team Monitors completeness and quality of the Clinical TMF, including elements outsourced to CRO Ensures effective communication and issue escalation internally and with external vendors Oversees consolidation and archive preparation of clinical TMF, liaising with CRO partners to ensure compliance with company SOPs and timelines throughout the process. Ensures compilation of CSR appendices in accordance with Shire’s process Supports inspection readiness for GCDO through periodic quality assessment of clinical records. Ensures clinical records are filed in a timely manner With direction from the CDM Manager, prepares clinical records for agency inspection. Supports assigned TMF corrective action plans under direction of Senior CDM/Manager. Supports CDM initiatives to enhance efficiencies in document management practices Supports Managers in training efforts for new personnel Education and Experience Requirements Minimum 2 years of pharmaceutical industry experience Records management/TMF experience Familiarity with various aspects of clinical trials and regulatory submissions . Current awareness of regulatory requirements for clinical trials (ICH/GCP). Associates/Bachelor’s degree or equivalent preferred Key Skills, Abilities, and Competencies Sufficient knowledge of regulatory requirements and ICH-GCP guidelines to support records management Demonstrated ability to work independently, take initiative, complete tasks to deadlines Requires strong attention to detail, document organization skills, establishing priorities, scheduling and meeting deadlines Solid communication skills and strong customer focus with ability to interact in a global, cross functional organization Ability to communicate effectively with external vendors, including issue escalation, and responding to enquiries and concerns Must be able to work in a fast paced environment with demonstrated ability to prioritize multiple competing tasks and demands. Experience with use of Electronic Document Management Systems Advanced computer proficiency Demonstrated ability to be flexible and to adapt quickly to change Ability to multi-task Internal and External Contacts Internal study team members within the R&D organization at various levels, global team colleagues; external vendors (CROs, other service providers) Other Job Requirements Full driving license and passport required Domestic (within country) and some potential international travel possible (10%) Kind Regards , Sasha Sharma Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO DIRECT # - 732-662-7964 Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.