Copywriting Senior Analyst – Medical Affairs
Company: Accenture
Location: Mumbai
Employment Type: Full Time
Job No.: AIOC-S01654708
Domain: Marketing Operations – Medical Affairs
Job Summary
The Copywriting Senior Analyst role focuses on developing high-quality medical and scientific content for pharmaceutical and life sciences clients. The position involves medical writing, scientific communication, regulatory content review, Medical Legal Regulatory (MLR) compliance, and development of promotional and educational materials across various healthcare communication channels.
The role requires strong expertise in translating complex clinical data into clear, accurate, and engaging medical content while collaborating with medical, regulatory, creative, and technology teams.
Key Responsibilities
Medical Writing & Content Development
Develop medical/scientific content for clinical and regulatory documents following industry guidelines.
Create content outlines and provide scientific guidance for assigned projects.
Develop materials including:
White papers
Manuscripts
Scientific narratives
Point-of-view documents
Medical education materials
Brand communication content
Interpret clinical data and communicate scientific information clearly and accurately.
Perform medical review of documents while ensuring scientific accuracy and compliance.
Medical Affairs & Promotional Content
Develop medical communication content for pharmaceutical brands.
Create content for marketing communication channels such as:
Veeva-approved emails
Veeva CLMs (Closed Loop Marketing)
Medical/brand websites
Videos
Digital healthcare solutions
Support medical communication strategies across different product lifecycle stages.
Provide scientific input for brand strategy and medical education initiatives.
Regulatory & Compliance Activities
Ensure compliance with:
Medical Legal Regulatory (MLR) review processes
Regulatory guidelines
Client SOPs
Accenture internal quality standards
Prepare and submit content artifacts through platforms such as Veeva Vault PromoMats.
Perform referencing, annotation, and documentation activities.
Maintain audit readiness and ensure quality documentation.
Project Management & Collaboration
Manage project execution, timelines, tracking, and delivery.
Coordinate with:
Medical writers
Scientific teams
Operations teams
Technology teams
Creative teams
Support client communication, status reporting, and action tracking.
Identify process improvement opportunities.
Monitor project metrics including timelines and task completion.
Leadership & Mentoring
Guide junior medical writers and support skill development.
Provide intellectual input across multiple document types.
Support client presentations, pitches, and business development activities.
Manage small teams or project workstreams when required.
Required Qualifications
Education
Graduate degree required.
Preferred qualifications:
MBBS
MD
M.Pharm
Life Sciences-related degree
Experience Required
5–7 years of relevant experience in medical writing or scientific communications.
Strong experience in pharmaceutical, healthcare, or life sciences industry.
Experience in medical affairs, promotional medical communication, or healthcare agencies preferred.
Experience creating scientific content for global pharmaceutical brands.
Technical & Domain Skills
Medical Writing Expertise
Strong understanding of:
Clinical research methodology
Scientific literature review
Clinical data interpretation
Medical terminology
Regulatory communication requirements
Therapy Area Experience
Preferred experience in specialized therapy areas such as:
Oncology
Respiratory
Cardiology
Dermatology
Vaccines
Infectious Diseases
Nephrology
Rare Diseases
Tools & Platforms
Veeva Vault PromoMats
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Adobe Acrobat
Key Competencies
Excellent written and verbal communication skills.
Strong scientific and analytical abilities.
Ability to simplify complex clinical information.
High attention to detail and quality standards.
Ability to manage multiple projects simultaneously.
Strong understanding of pharma compliance requirements.
Ability to work independently and collaborate with global teams.
Knowledge of current medical literature and healthcare trends.
Uttar Pradesh :
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