Program Manager Regulatory Medical Writing

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profile Job Location:

Morrisville, NC - USA

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as a Program Manager within our Regulatory Medical Writing team where you will make an Impact at the Forefront of Innovation.
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.

As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Regulatory Medical Writing Program Manager you will lead client programs with high visibility among internal and client teams often requiring a high degree of client engagement and management; manage client relationships and identify and resolve client management issues; manage and ensure the timely delivery and the quality of multiple program documents; develop monitor and adapt project plans client and program-specific processes timelines and budgets/forecasting for programs. You will also serve as subject matter expert for assigned programs.

What Youll Do:

  • Develop project timelines standards budgets forecasts and contract modifications for assigned projects. Serves as liaison with other departments on contract modifications.
  • Assist business development and senior management on securing new business at program levels by developing and making presentations to clients leading the development and review of proposal texts and budgets and supporting contract negotiations.
  • Serve as point of contact for risk escalation for assigned programs. Evaluates and appropriately escalates or resolves risks to project quality budget or timeline.
  • Ensure compliance with quality processes and requirements for assigned programs both within and between documents within a project. Develops reviews and manages performance metrics for assigned projects.
  • Provide training for medical writers on processes and technical aspects of program management.
  • May serve as backup medical writer. Duties could include researching writing and editing clinical study reports and protocols summarizing data from clinical studies writing or providing input on complex clinical and scientific documents such as IBs INDs and MAAs and providing senior review of project materials.


Education and Experience Requirements:

  • Bachelors degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
  • Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 8 years).
  • Experience in managing and directing complex medical writing projects required
  • Experience working in the pharmaceutical/CRO industry preferred
  • Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous

In some cases an equivalency consisting of a combination of appropriate education training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.


Knowledge Skills and Abilities:

  • Solid program management skills to include budgeting forecasting and resource management
  • Extensive knowledge of global regional national and other document development guidelines
  • In-depth knowledge in one or more specialty areas such as preclinical therapeutic regulatory submissions communications etc.
  • Excellent interpersonal oral and written communication and presentation skills
  • Excellent negotiation skills
  • Self-motivated and adaptable
  • Excellent judgment; high degree of independence in decision making and problem solving
  • Capable of mentoring and leading junior level staff


Why Join Us
When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthroughs.


Required Experience:

Manager

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as a Program Manager within our Regulatory Medical Writing team where you will make an Impact at the Forefront of Innovation.We have successfully supported the top 50 pharmaceutical companies and more than 750 biotec...
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Key Skills

  • Project Management Methodology
  • Project / Program Management
  • Program Management
  • Management Experience
  • Microsoft Powerpoint
  • Project Management
  • Microsoft Project
  • Budgeting
  • DoD Experience
  • Leadership Experience
  • Supervising Experience
  • Contracts

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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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