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REGULATORY/MEDICAL WRITING PROJECT MANAGER

Descripción de la oferta de empleo

The Project Manager, Medical/Regulatory Writing (PM) is the main point of contact for clients at TransPerfect. The PM will be responsible for day to day project management and oversight of medical writing projects, with an special focus on regulatory documents (Protocols, CSR, IB etc), and will be in daily and regular contact with clients. The PM will also be responsible for keeping up-to-date SOPs regarding medical writing processes. The PM will be required to meet all client timelines and work in conjunction with the medical writing manager, medical writers, and account managers, and will be accountable for the success of all medical writing projects. This role reports directly to the Senior Team Lead of TransPerfect’s Medical Writing division. Responsibilities include, but are not limited to:Oversee all elements of medical writing projects, and set and fulfill client expectationsOversee project budgets and monitor costs against Client Budget and Statement of WorkMonitor and communicate project progress, ensure strict adherence to deadlines and budgets, and ultimately produce high quality deliverablesPartner with medical writing vendor manager to build pool of medical writing resources, and weigh in on resource gaps and growth marketsServe as the primary point of contact for client contactsRespond to client requests for new project initiatives; collaborate with various departments to assess the scope of work and produce cost estimatesGrow existing client relationships through service and technology lead developmentTake a proactive role in learning about clients’ industry and business needs and company culture, educating the project team, identifying new business opportunities, and providing a high level of serviceComplete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor Required Skills/Qualifications:Minimum Master’s Degree or PHD or equivalentAbout 2-4 years’ of experience in the Life Sciences industry with a focus on regulatory writing (pharmaceutical, biotechnology or CRO experience preferred)Experience in customer serviceAble to multitask in a fast-paced environmentKnowledge of clinical development phases and processesSuperior written and spoken communication skills in EnglishExceptional problem solving/critical thinking skillsProficiency in Microsoft Office (Word, Excel, Outlook)By applying, I confirm I have read and accept TransPerfect's Privacy Policy: https://www.transperfect.com/about/data-privacy-recruiting
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Detalles de la oferta

Empresa
  • TransPerfect
Localidad
  • En toda España
Dirección
  • Sin especificar - Sin especificar
Fecha de publicación
  • 10/09/2024
Fecha de expiración
  • 09/12/2024
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