Medical Writer II

1 - 6 years

8 - 9 Lacs

Posted:4 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Mentors less experienced medical writers on projects, as necessary.
  • Compiles, writes, and edits medical writing deliverables, and serves as a medical writer within and across departments with minimal supervision.
  • Develops or supports a variety of documents that include but not limited to:
  • o Clinical study protocols and clinical study protocol amendments;
  • o Clinical study reports;
  • o Patient narratives;
  • o Annual reports;
  • o Investigator brochures.
  • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
  • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
  • Serves as peer reviewer on internal review team. Addresses team comments accurately to ensure document scientific content, clarity, overall consistency, and proper format.
  • Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
  • Performs on-line clinical literature searches, as applicable.
  • Working knowledge of drug development process and regulatory guidelines.
  • Continues professional development to keep pace with regulatory guidance and client expectations in medical writing that affect medical writing.
  • Stays aware of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
  • Completes required administrated tasks within the specified timeframes.
  • Performs other work-related duties as assigned.
  • Minimal travel may be required (less than 25%).

Qualifications - External
What we re looking for
Should have Min 1 years of experience working in narratives with masters qualification and 2 years experience with Graduation. Must have good experience in drafting and reviewing narratives.
Should be a Postgraduate (Masters /Mpharm ) or bachelor s degree.
Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide. Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership skills and ensure a team-oriented approach. Strong proficiency in Word, Excel, PowerPoint, email, and Internet. Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.

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