Principal Medical Writer
Parexel International Corporation
Hackensack, NJ(remote)
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JOB DETAILS
SKILLS
Analysis Skills, Biology, Budget Management, Business Development, Clinical Data, Clinical Research, Clinical Study Publications, Corrective Action, Customer Relations, Develop and Maintain Customers, Document Management, Documentation, Drug Development, English Language, Financial Projections, Forecasting, Health Science, Incident Response, Information Technology & Information Systems, Leadership, Maintain Compliance, Medical Records, Medical Research, Medical Writing, Mentoring, Metrics, Microsoft Office, Microsoft SharePoint, Microsoft Word, Organizational Skills, People Management, Performance Analysis, Performance Management, Performance Reviews, Pricing, Problem Solving Skills, Process Improvement, Productivity Management, Program Evaluation, Project Planning, Project Tracking, Project/Program Management, Proposal Development, Regulations, Regulatory Submissions, Resource Management, Sales, Sales Presentation, Software Evaluation, Staff Requirements, Standard Operating Procedures (SOP), Strategic Planning, Team Player, Technical Leadership, Time Management, Training/Teaching, Willing to Travel, Word Processing, Writing Skills
LOCATION
Hackensack, NJ
POSTED
30+ days ago
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.
About the Company
P
Parexel International Corporation
The expertise and passion for excellence shared by our people around the world unites us in our mission and drives our success. As a premier service provider to the global biopharmaceutical industry, we give you the opportunity to work with industry-leading clients in an exciting, collaborative environment where career choices and development paths are abundant, and projects are challenging. In fact, PAREXEL works with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. With over 30 years of experience, we have supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market.
We offer our employees the ability to make a difference globally, while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential.
Discover a career at PAREXEL, where exciting challenges and opportunities await you.
COMPANY SIZE
10,000 employees or moreINDUSTRY
All
FOUNDED
1982
WEBSITE
http://www.parexel.com