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Document Specialist I

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
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Offer summary

Qualifications:

Bachelor's degree or equivalent experience in a related field., Proficiency in MS Word and familiarity with document formatting standards., Understanding of global regulatory submission formats and industry guidelines., Ability to work independently and manage multiple tasks effectively..

Key responsabilities:

  • Compile appendices to clinical study reports and ensure compliance with regulatory requirements.
  • Perform document formatting and quality control to ensure submission readiness.
  • Serve as a contact for document compilation and publishing projects, managing timelines and deliverables.
  • Attend meetings and provide administrative support as needed.

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Parexel XLarge http://www.parexel.com
10001 Employees
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The Document Specialist I will provide document technology support on Medical Writing projects as appropriate. Some specific responsibilities include compilation of appendices to clinical study reports and similar documents, document formatting and post PDF work, document scanning/uploading, preparation of electronic appendices using departmental publishing workstation, and organizing and tracking all deliverables.

The Document Specialist I must be conscientious, able to work with minimal supervision, have an aptitude for working with a variety of different software applications and systems, exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle matters of a confidential nature.

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.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Word
  • Quality Control
  • Physical Flexibility
  • Time Management
  • Teamwork
  • Communication
  • Problem Solving

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