Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Medical Writer

1-4 years years
upto 7.5 LPA
5 July 15, 2024
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm/PharmD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Medical Writer

 

Location: India (Remote)

Company: Parexel


Overview

About this Role:
As a Senior Medical Writer at Parexel, you will utilize your strong scientific knowledge, writing skills, and patient focus to effectively communicate complex scientific data to various stakeholders, including regulatory agencies, medical professionals, and the general public. You will collaborate within cross-functional teams to develop a wide range of clinical research documents, such as model informed consent forms, clinical study reports, pharmacovigilance documents, and more.

Our Culture:
We foster a culture of inclusivity, collaboration, and support that empowers our employees to make a meaningful impact on people's lives. We offer continuous learning opportunities, from being mentored to job shadowing, job rotation, and stretch assignments, as well as becoming a mentor or leading a team. Your development and promotion are based on global standards and your personal development plan.


Success Profile

Essential Soft Skills and Traits:

  • Adaptable
  • Communicator
  • Consistent
  • Deadline-oriented
  • Detail-oriented
  • Insightful

About This Role

Position: Senior Medical Writer

Key Responsibilities:

  • Research, create, and edit all documents associated with clinical research.
  • Operate as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related documents.
  • Facilitate process improvement and technical mentoring/training.
  • Support Medical Writing Services management during the sales process by providing client liaison and proposals input.

 

Minimum Qualification Requirements:

  • 6+ years of experience in regulatory medical writing.
  • Experience in authoring protocols, clinical study reports, investigator’s brochures, informed consent forms, summary documents, etc.
  • Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders, gastrointestinal disorders, infectious diseases, mental health, neurology, oncology, etc.
  • Strong communication and interpersonal skills.
  • Bachelor’s or advanced degree in life sciences/healthcare.
  • Experience from the pharmaceutical/CRO industry.
  • Ability to work independently and lead projects.
  • Strong analytical skills.
  • Commitment to highest quality outputs, including high attention to detail.
  • Ability to manage variable workload.

 

Apply Now: Please visit Parexel Careers for more information and to submit your application.