Document Specialist I

Document Specialist I
BengaluruM.Sc/B.Sc/B.Pharma/M.Pharm/Life Science

Document Specialist I

Compilation and publishing

  • Compile appendices to clinical study reports in compliance with appropriate regulatory requirements, with support of the project lead and lead medical writer. Work with internal or external Clinical and/or Project Leadership functions to ensure that appendix documentation is complete and complies with the relevant guidelines.
  • Understands global regulatory submission formats, industry standards, and guidelines, and publishing best practices
  • Use departmental publishing software to produce electronic deliverables to ensure insertion of navigability features, and accurate intra-document hyperlinking, according to SOP/client/regulatory requirements
  • Perform MS Word formatting of clinical documents according to SOP/client/regulatory requirements. Insert tables if requested. Coordinate production and distribution of draft and final documents to project team and client. Organize and track delivery of all deliverables.
  • Ensure that all work is complete and of high quality prior to delivery
  • Provide support on software and document related issues to MWS staff as required

Quality Control

  • Ensure that all work is complete and of high quality prior to team distribution or shipment to client.
  • Ensure document is submission ready as per the appropriate regulatory guidelines, and comply with departmental, corporate or client SOPs and style guidelines, as applicable
  • Under appropriate supervision as needed, provide review of draft and final documents prepared by other DS before internal or external distribution

Document Project Management

  • Under departmental supervision, serve as contact for compilation and publishing projects, supports negotiating deliverable timelines, and resolving project-related issues.
  • Serve as the Document Specialist representative on assigned project, with departmental supervision:
  • communicate requirements, conduct team review of draft and final documents, attend study team meetings to agree on expectations, inform about the timeline, and advance document publishing to approval, according to PAREXEL or client guidelines/SOPs.
  • Distribute final documents to project team and client only if agreed.
  • Perform collection of documentation for assembly of project files and client deliverables. Ensure appropriate filing of project documentation with assistance from the Medical Writing Support Coordinator.
  • Project management of contractual and financial aspects may only be performed with the guidance of medical writing management

Training/ Compliance

  • Attend and complete mandatory, corporate, project-specific, and departmental training as required.
  • Assist in the training/mentoring of new departmental staff as required.

General

  • Attend departmental and company meetings as necessary. Comply with departmental procedures and requirements, such as completion of project assignment and workload trackers on the applicable software platform.
  • Provide administrative support if requested.

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers quality solutions to make every phase of the clinical trial process more efficient. Our top-notch people, insight, and focus on operational excellence allow us to work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. This approach continues to earn us recognition industrywide, with Parexel being the recipient of the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award for advancing the clinical research profession through strong site partnerships and named “Top CRO to Work With” by investigative sites worldwide in the 2023 WCG CenterWatch Global Site Relationship Benchmark Survey.

Job Overview

Location: Bengaluru

Qualification: M.Sc/B.Sc/B.Pharma/M.Pharm/Life Science

Experience: 02+ Years