Content Copywriter
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Monthly Salary:
Posted on:
16 hours ago
Vacancies:
1 Vacancy
Job Summary
Job Title: Medical Writer
Level: Sr Analyst
Reports To: Senior Manager
Location: India
Overall Purpose of the Job
The Medical Writer is responsible for developing high-quality scientific and medical content for marketing clinical and regulatory purposes. This includes creating submission-ready documents ensuring compliance with medical legal and regulatory standards and serving as the subject matter expert for scientific writing within the team.
Key Responsibilities
Content Development:
o Create accurate clear and compliant medical communications for various channels (e.g. Veeva-approved emails CLMs websites videos).
o Draft and review promotional and educational materials for medical affairs.
Regulatory & Compliance:
o Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
o Manage referencing and annotation in Veeva Vault PromoMats.
Scientific Expertise:
o Interpret and document clinical data accurately.
o Conduct literature searches and analyze client assets for evidence-based content.
Collaboration:
o Communicate effectively with cross-functional stakeholders to meet timelines.
o Provide intellectual input across multiple therapy areas (oncology respiratory cardiology dermatology vaccines infectious diseases nephrology rare diseases).
Qualifications
Experience:
o 5 10 years in medical writing or related roles in pharma/life sciences.
o Prior experience in medical communications and regulatory documentation.
Skills:
o Strong understanding of therapy areas and regulatory guidelines.
o Excellent writing editing and communication skills.
o Familiarity with Veeva systems and MLR processes
Preferred Attributes
Ability to work independently and manage multiple projects.
Strategic thinking and creativity in content development.
Strong problem-solving and critical thinking skills.
Level: Sr Analyst
Reports To: Senior Manager
Location: India
Overall Purpose of the Job
The Medical Writer is responsible for developing high-quality scientific and medical content for marketing clinical and regulatory purposes. This includes creating submission-ready documents ensuring compliance with medical legal and regulatory standards and serving as the subject matter expert for scientific writing within the team.
Key Responsibilities
Content Development:
o Create accurate clear and compliant medical communications for various channels (e.g. Veeva-approved emails CLMs websites videos).
o Draft and review promotional and educational materials for medical affairs.
Regulatory & Compliance:
o Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
o Manage referencing and annotation in Veeva Vault PromoMats.
Scientific Expertise:
o Interpret and document clinical data accurately.
o Conduct literature searches and analyze client assets for evidence-based content.
Collaboration:
o Communicate effectively with cross-functional stakeholders to meet timelines.
o Provide intellectual input across multiple therapy areas (oncology respiratory cardiology dermatology vaccines infectious diseases nephrology rare diseases).
Qualifications
Experience:
o 5 10 years in medical writing or related roles in pharma/life sciences.
o Prior experience in medical communications and regulatory documentation.
Skills:
o Strong understanding of therapy areas and regulatory guidelines.
o Excellent writing editing and communication skills.
o Familiarity with Veeva systems and MLR processes
Preferred Attributes
Ability to work independently and manage multiple projects.
Strategic thinking and creativity in content development.
Strong problem-solving and critical thinking skills.
Key Skills
- Presentation Skills
- Marketing
- Proofreading
- Copy Editing
- Adobe Creative Suite
- Multichannel Marketing
- SEO
- Alternative dispute resolution
- Copywriting
- Creative Writing
- Branding
- Writing Skills
