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Medical Writer I

0-2 years
Not Disclosed
10 March 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Medical Writer I
Location: India, Remote
Company: Parexel

Job Purpose:

Responsible for the management of scheduled and unscheduled aggregate reports, including but not limited to:

  • Periodic Safety Reports (PSRs)

  • Periodic Safety Update Reports (PSURs)

  • Periodic Benefit-Risk Evaluation Reports (PBRERs)

  • Addendum to Clinical Overviews (ACOs)

  • Semi-Annual Safety Reports (SASRs)

  • United States Periodic Adverse Drug Experience Reports (PADERs)

  • Development Safety Update Reports (DSURs)

  • Annual Risk-Benefit Evaluation (ARBE) Reports

  • Risk Management Plans (RMPs)

  • Safety statements, Health Hazard Evaluations (HHEs), and Drug Safety Reports (DSRs)

Additionally, responsible for preparing narratives associated with the client’s/sponsor’s products, supporting health authority requests, and ensuring compliance with regulatory and client standards.


Key Accountabilities:

Aggregate Reports:

  • Prepare, update, and merge RMPs/Company Core-RMPs (CC-RMPs).

  • Develop health authority response documents and ensure compliance with SOPs.

  • Conduct critical appraisal and systematic review of literature, focusing on background epidemiology for inclusion in drug safety reports and RMPs.

  • Generate line listings for submissions and identify discrepancies for resolution.

  • Ensure document consistency and integrity across various aggregate reports.

  • Perform compliance reviews of aggregate reports, ensuring adherence to regulatory and client timelines.

Clinical Study Report Narratives:

  • Prepare clear and accurate narratives based on Clinical and Safety Database outputs.

  • Perform quality checks on drafted narratives and assist in formatting narrative deliverables.

Signal Detection and Management:

  • Perform signal detection review and analysis from regulatory databases, client databases, literature, and authority websites.

  • Lead end-to-end signal management processes, including tracking, assessment, and presenting findings.

General Responsibilities:

  • Maintain knowledge of adverse event safety profiles and international drug safety regulations.

  • Ensure timely compliance with internal and regulatory timelines for adverse event reporting.

  • Support audits and inspections, ensuring awareness of performance metrics and striving for client satisfaction.

  • Mentor new recruits when required and archive relevant documents and correspondence.


Skills:

  • Strong analytical and problem-solving skills

  • Excellent interpersonal, verbal, and written communication skills

  • Strong organizational and prioritization abilities

  • Ability to evaluate data, draw conclusions independently, and manage multiple tasks effectively

  • Proficiency in MS Office and web-based applications

  • Awareness of global culture and the ability to work in a matrix environment


Knowledge and Experience:

  • Relevant experience in Regulatory, Pharmacovigilance, or a related field is desirable.

  • Strong knowledge of medical terminologies.


Education:

  • Minimum: University degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)

  • Preferred: Degree in Medicine, Dentistry, Physiotherapy, Experimental Medicine, or Nursing with hospital-based patient exposure.