Instagram
youtube
Facebook

Medical Writer I

0-2 years
Not Disclosed
10 Jan. 3, 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 – Parexel
Remote Position

At Parexel, we transform lives through innovative clinical research and medical writing. As a Medical Writer, you will translate complex scientific data into clear, effective communication for diverse audiences, including regulatory agencies, healthcare professionals, and the public. Your work will directly support the development of groundbreaking treatments, fostering patient-focused care.


About Parexel

We pride ourselves on inclusivity, collaboration, and support. Our culture encourages professional growth through mentoring, job shadowing, rotations, and leadership opportunities. Career progression is guided by global standards and your personalized development plan.


Job Purpose

You will manage and develop key clinical research documents such as:

  • Aggregate Reports (e.g., PSURs, PBRERs, DSURs).
  • Clinical Study Reports (CSRs) and related narratives.
  • Regulatory Submissions and safety documents.
  • Literature reviews, risk management plans, and signal detection activities.

Key Responsibilities

Aggregate Reports

  • Prepare/manage reports, including PSURs, PBRERs, and DSURs.
  • Conduct critical literature reviews for epidemiological data inclusion.
  • Ensure quality and consistency across all reports and documents.
  • Handle submissions and compliance tracking.

Clinical Study Report Narratives

  • Develop clear and accurate narratives based on clinical and safety databases.
  • Perform quality checks and formatting for deliverables.

Signal Detection and Management

  • Analyze signals from regulatory and clinical sources.
  • Conduct end-to-end signal management, including meetings and assessments.

General Responsibilities

  • Maintain knowledge of drug safety profiles, labeling documents, and regulations.
  • Act as a primary client contact, ensuring satisfaction and delivering high-quality work.
  • Mentor junior team members and ensure timely responses to clients.

Skills & Competencies

  • Strong analytical, organizational, and problem-solving skills.
  • Excellent written and verbal communication.
  • Ability to prioritize multiple tasks while maintaining attention to detail.
  • Familiarity with global regulatory guidelines and medical terminologies.
  • Proficiency in IT tools, web applications, and MS Office Suite.

Knowledge & Experience

  • Prior experience in regulatory, pharmacovigilance, or related fields is desirable.
  • Knowledge of clinical studies and drug safety.

Educational Qualifications

  • Bachelor’s degree in Life Sciences/Health/Biomedical Sciences (e.g., Pharmacy, Biotechnology).
  • Advanced degrees (e.g., MD, Dentistry, Nursing) with hospital exposure are advantageous.

Success Profile

At Parexel, success is driven by soft skills like adaptability, communication, detail orientation, and a client-focused approach.


Why Choose Parexel?

  • A supportive culture fostering innovation and teamwork.
  • Professional development opportunities tailored to your goals.
  • Remote working flexibility.

Join Parexel and contribute to clinical research that makes a global impact. Apply now to be part of our mission to improve lives through science and collaboration.