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Expert scientific / Medical writer

1.00 to 3.00 Years   Vadodara   12 Dec, 2021
Genpro Research
Job LocationVadodara
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaSales / BD
EmploymentTypeFull-time

Job Description

To author and complete Medical Communications deliverables independently as per high quality standards (internal external) and within expected timelines. Deliverables include manuscripts, slide sets, abstracts, posters, medical education materials, systematic reviews and other techno-commercial documents. Support regulatory medical writing deliverables like CSR, Protocols, IB etc.

Key activities:

  • Author original content for publications activities like primary/review manuscripts, abstracts, posters; slide decks etc based on specific inputs and sources supplied by customers.
  • Author deliverables with scientific accuracy, based on facts from available sources and meeting quality standards (including grammar and editorial requirements).
  • Follow all internal and/or client processes and adhere to GPP3 and other industry best practices.
  • Undertake quality control (QC, scientific reviews and/or proof reading of the above-mentioned deliverables.
  • Showcase flexibility in terms of timelines and writing style based on client needs and/or therapeutic area requirements across various domains.
  • Conduct client/KOL interactions, kickoff meetings and teleconferences as needed covering various time zones in an effective manner.
  • Conduct thorough literature search and interpretations to support scientific advisory services.
  • Design and conduct robust training programs for the team.
  • Support in SOP, work-instructions and other documentation development and/or maintenance and keep the department audit ready at all the instances.
  • Support proactively in business expansion department operation activities as needed.
  • Undertake additional tasks as assigned.

Required Skills / Experience

  • The candidate should be a Science graduate/equivalent
  • PhD, PharmD, MPharm or MD (desirable)
  • At least 5 years of experience in Scientific writing and communications either in Global pharma and/or service industry.
  • Mix of publication and regulatory writing will be a plus.
  • Thorough understanding of industry standards and global trends.
  • Highly proficient in MS Office products.

Work Location: Baroda, Gujarat. Remote work possible after one year for deserving candidate with proven track record.

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Keyskills :
clinical trialssafetyprotocolsresearchliteraturehigh quality standardsms officeslide decksproof readingquality controlmedical writingtherapeutic areaquality standardsmedical educationtraining programsscientific writingbusiness expansion

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