Thermo Fisher Scientific is hiring Medical Writer – B. Pharma/ M. Pharma freshers can apply

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Thermo Fisher Scientific is seeking passionate B. Pharma and M. Pharma freshers for the role of Medical Writer in a work-from-home position. This is an excellent opportunity for recent graduates to kickstart their careers with a leading global biotechnology company. Join Thermo Fisher Scientific and contribute to impactful medical writing projects from the comfort of your home. Apply now to be part of a team dedicated to advancing scientific research and healthcare solutions.

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO).

Position Medical Writer
Category Clinical research
Education B. Pharma/ M. Pharma
Experience

Freshers

Experience working in the pharmaceutical/CRO industry preferred.
Experience in scientific writing advantageous.
Experience in the therapeutic areas of Immunology, Oncology or Vaccines advantageous.

Job Description
Summarized Purpose:

We are excited to expand our India Medical Writing FSP Team! We are looking for a Medical Writer to be dedicated to a client in the FSP space; experience in Immunology, Oncology or Vaccines would be valuable but not essential. The writer will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Essential Functions:

  • Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.
    May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
  • Ensures compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods, and techniques for achieving optimal results.
  • May assist in program management activities. Duties could include assisting with developing timelines, budgets, forecasts for assigned deliverables.
  • Represents the department at project launch meetings, review meetings, and project team meetings.

Knowledge, Skills, and Abilities:

  • Solid medical writing skills, including grammatical, editorial, and proofreading skills.
  • Ability to interpret and present complex data accurately and concisely.
  • Effective administrative, organizational, and planning skills; attention to detail and quality
  • Ability to work on own initiative and effectively within a team.
  • Effective oral and written communication skills
  • Good knowledge of regulatory documentation and drug development process
  • Great judgment and decision-making skills
  • Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
Job Location Work From Home
Job ID R-01242044
Job Type Full Time
Apply Online Click Here

 

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