SENIOR EXECUTIVE

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Date: Jan 7, 2026

Location: Bangalore, KA, IN

Company: bioconbiolP2

Company Overview

Role Purpose

The Specialist – Medical Writing is responsible for creating, reviewing, and managing high-quality scientific documents that support clinical development, regulatory submissions, medical communications, and medical affairs activities. This role ensures that all medical writing outputs are scientifically accurate, clear, compliant with regulatory standards, and aligned with the company’s therapeutic and medical strategies. The Specialist collaborates closely with cross-functional teams to translate complex clinical data into understandable, well-structured, and impactful written materials.

Academic Stream

0

Work experience (in months)

0

Job Responsibility and key Decisions

Document Development

Write, review, and edit a variety of clinical and medical documents including protocols, amendments, CSRs, investigator brochures, and regulatory submissions.

Medical Communication Support

Develop scientific content for medical education materials, presentations, posters, and publications.

CrossFunctional Collaboration

Work closely with clinical teams, regulatory affairs, biostatistics, and medical affairs to gather data and ensure scientific accuracy.

Compliance and Quality Control

Ensure all documents comply with regulatory guidelines, ethical standards, and company policies.

Project Management

Manage timelines and coordinate inputs from multiple stakeholders to deliver documents on schedule.

Continuous Improvement

Participate in improving medical writing processes, templates, and standards.

Scientific Content Development Author, review, edit medical documents and develop content for scientific publications, abstracts, posters, and manuscripts in collaboration with internal and external stakeholders.

Medical Education Communication Create materials for medical education programs, advisory boards, and symposia. And Translate complex scientific data into clear, engaging content for diverse audiences including HCPs, KOLs, and internal teams.

CrossFunctional Collaboration Partner with Clinical Development, Regulatory Affairs, Pharmacovigilance, and Commercial teams to gather data and ensure scientific accuracy. Support publication planning and contribute to strategic communication initiatives.

Compliance Quality Assurance Ensure all documents adhere to ICHGCP, company SOPs, and applicable regulatory and ethical standards. Maintain auditready documentation and version control across all deliverables.

Insight Integration Strategy Incorporate field insights, clinical data, and realworld evidence into medical content to support strategic messaging. Contribute to the development and refinement of medical writing templates and style guides.

Project Stakeholder Management Manage timelines and coordinate inputs from internal teams and external authors to meet publication and communication deadlines. Track progress using project management tools and ensure timely delivery of highimpact content.

Key Decisions

Content Accuracy

Decide when to seek additional input or clarification to ensure scientific accuracy and completeness.

Document Formatting and Style

Determine the appropriate style and structure based on document type and audience.

Prioritization of Writing Tasks

Manage competing deadlines and prioritize writing assignments accordingly.

Compliance Adherence

Make decisions regarding compliance with SOPs and regulatory guidelines in document preparation.