Principal Medical Writer
Company: Parexel International Corporation
Location: Hackensack
Posted on: February 9, 2025
Job Description:
PXL is looking to hire a Principal Medical Writer ! This is a
fully remote role!Job Purpose: The Principal Medical Writer will
research, create, and edit all documents associated with clinical
research. The Principal Medical Writer may operate as the project
lead writer/submission coordinator
and primary client contact to manage contributions of multiple
writers working on related documents. The
Principal Medical Writer also facilitates process improvement and
technical mentoring/training and supports Medical Writing Services
management during the sales process by providing client liaison and
proposals inputKey Accountabilities:
Accountability
Supporting Activities
- Author Clinical Documents
- Gather, review, analyze, and evaluate pertinent resources to
prepare, develop,
- and finalize key clinical documents for submission to
regulatory authorities,
- without the need for any supervision or additional formal
on-the-job training.
- Train self and provide guidance to others to prepare any type
of
- medical writing deliverable.
- Revise document drafts based on the review comments from
team
- members to ensure inclusion of all relevant input.
- Manage ongoing and/or revised project documentation and
correspondenceQuality Control
- Ensure that all work is complete and of high quality prior to
team distribution or
- shipment to client.
- Provide technical leadership to ensure clinical data presented
in summary
- documents is in compliance with applicable regulatory
guidelines, SOPs,
- and goals of submission.Project
- Operate as the project lead writer/submission coordinator and
primary client
- Management contact to manage contributions of multiple writers
working on related documents. Manage scope of work, timeline and
project goals,
- technical information, and input from clients throughout the
project.
Develop, coordinate, and oversee work plans for individual and
multiple-
document delivery, to enable the team to work efficiently and
effectively to
meet milestones and achieve team objectives.
- Provide leadership and strategic planning/adjustments,
delegation of responsibilities, and tasks to team members. Monitor
the progress of each individual project task and assess the overall
program.
- Ensure key information received in project or program meetings
is
- appropriately disseminated, such that project strategy is
maintained and data or key message changes are incorporated
appropriately across documents.
- Continuously monitor overall project performance and, if
necessary,
- identify ways to ensure that the project is completed on-time
and within budget.
- Keep client and team informed of project status.
- Contribute expertise as a document/cross-document specialist
and content
- historian to analyze proposed program, studies, and related
documents to
- deliver information required by the target audiences.
- Build and maintain collaborative relationships with
teams/clients, leading to
- increased performance and a sense of inclusion. Cultivate
efficient,
- productive, and professional working relationships to promote
client
- satisfaction and confidence.
- Track actual versus planned project budget. Determine the cause
of cost
- overruns and out-of-scope activities and recommend corrective
action to
- medical writing management.
- Provide updates for each project to Medical Writing Services
management,
- and assess forecasting and resourcing. Propose creative
solutions to
- medical writing management to shifting timelines and staffing
requirements.
- Communicate to writer's line manager any needs or concerns
regarding level
- of training or performance of team members on project work.
Provide line
- manager with input regarding team member's performance for
employees'
- periodic performance review, and as neededClient
Liaison/Service
- Be aware of client expectations for self and team members.
- Respond appropriately to incidents of dissatisfaction, and feed
back to Medical Writing Services management.
- Provide support as appropriate to Business Development/Client
Solutions and
- Medical Writing Services management in their efforts to win new
business.
- Identify and solicit new business leads for Medical Writing
Services, attend
- business development meetings, and prepare and make sales
presentations to clients, if called upon.
- Provide strategic and project planning intelligence to Medical
Writing Services management for medical writing activities in the
proposal generation process, including assessment of scope of
services to be provided to a client with respect to medical writing
tasks.
- May attend proposal development meetings if requested by
Medical Writing Services management.
- Input to development of client proposals generated by Medical
Writing Services and letters of agreement/intent based on existing
templates.
- May function as the client contact if requested and communicate
pricing information conjunction with Medical Writing Services
management.
If requested, suggest appropriate resourcing, based on existing
templates
and standards, for full-service and stand-alone projects.Training
- Keep abreast of new advances in medical writing and regulatory
issues.
- Compliance
- Develop and train Medical Writing Services staff to enhance
writing
- quality, efficiency, and project management.
- Implement and monitor departmental compliance to SOPs.
Input
- to development or revision of departmental SOPs, as
appropriate.
- Develop and present external training courses.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
- Analyze efficiency of work and discuss improvement ideas with
Medical Writing Services management and colleagues, e.g.,
evaluation of software to increase productivity and document
qualityKnowledge and Experience
- Demonstrated understanding of clinical research, the drug
development process, and applicable regulatory guidelines and
regulations.
- Broad experience in preparation of all types of clinical
regulatory documentation. Experience in management of complex
medical writing projects.
- Knowledge of resource management and productivity metric
management.
- Advanced word processing skills, including MS Office (expertise
in Word); software and systems knowledge or ability to learn and
adapt to various IT systems: document management systems,
collaborative authoring (e.g., SharePoint), and file conversion and
databases (Excel).
- Ability to travel.
- Fluent in written and spoken English.Education:
Bachelor's degree in Life Sciences/Health Related Sciences or
equivalent.
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will
receive consideration for employment without regard to legally
protected status, which in the United States includes race, color,
religion, sex, sexual orientation, gender identity, national
origin, disability, or protected veteran status.
Keywords: Parexel International Corporation, Hackensack , Principal Medical Writer, Other , Hackensack, New Jersey
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