Masuu Global hiring Senior Medical Writer
- Masuu Global Hiring Senior Medical Writer in Hyderabad for Regulatory & Clinical Documentation
- Company Overview
- Job Role & Responsibilities
- Senior Medical Writer / Regulatory Medical Writer
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Relevant Courses
- Experience Required
- Required Skills
- Why Medical Writing Is a High-Demand Pharma Career
- Location & Salary
- Job Location
- Work Mode
- Expected Salary
- Application Process
- Email ID
- Subject Line
- Official Website
- Frequently Asked Questions (FAQs)
- Which company is hiring Medical Writers in Hyderabad?
- What qualifications are eligible for this role?
- What experience is required?
- What skills are preferred for this position?
- Is this a work-from-home role?
- How can candidates apply?
- Summary Table
Masuu Global Hiring Senior Medical Writer in Hyderabad for Regulatory & Clinical Documentation
Masuu Global Solutions is hiring experienced Medical Writing professionals for Senior Medical Writer and Regulatory Medical Writer roles in Hyderabad. Candidates with experience in regulatory documentation, clinical writing, pharmacovigilance documentation, and eCTD submissions can apply for this pharmaceutical regulatory writing opportunity.
The company is looking for professionals with expertise in CTD module writing, aggregate safety reports, clinical protocols, Investigator’s Brochures, and global regulatory submission documentation aligned with ICH, EMA, and MHRA guidelines.
Company Overview
Masuu Global Solutions is a pharmaceutical regulatory, quality services, and software company supporting global pharmaceutical and healthcare organizations.
The company provides services in:
- Regulatory Affairs
- Medical Writing
- Pharmacovigilance documentation
- eCTD publishing
- Quality compliance systems
- Regulatory submission support
- Clinical documentation management
- Aggregate safety reporting
Medical Writing and Regulatory Documentation professionals play a critical role in pharmaceutical product development and global regulatory approvals.
Professionals working in regulatory medical writing gain exposure to:
- Global drug development programs
- CTD and eCTD submissions
- Clinical and safety documentation
- Regulatory compliance systems
- Aggregate safety reporting
- International pharmaceutical guidelines
- Scientific writing and interpretation
Job Role & Responsibilities
Masuu Global Solutions is hiring for the following role:
Senior Medical Writer / Regulatory Medical Writer
Selected candidates will support global regulatory documentation and clinical writing projects.
Key Responsibilities
- Author and manage CTD Modules 2.4, 2.5, 2.6, and 2.7
- Prepare clinical protocols, CSRs, CTRs, and Investigator’s Brochures
- Support eCTD submission documentation
- Develop aggregate safety reports including:
- RMPs
- PSURs
- PBRERs
- PADERs
- Prepare pediatric regulatory submission documents including iPSP and PIP
- Conduct scientific literature searches and data interpretation
- Ensure compliance with ICH, EMA, and MHRA guidelines
- Coordinate with Regulatory Affairs, QA, Pharmacovigilance, and IT teams
- Manage project timelines, deliverables, and client communication
- Maintain documentation accuracy and regulatory compliance standards
Eligibility / Qualifications
Educational Qualification
Candidates with the following qualifications are eligible:
- B.Pharm
- M.Pharm
- Life Sciences
- Biotechnology
- Medicine
- Related Healthcare or Scientific Degrees
Relevant Courses
Medical Writing, Regulatory Affairs, Clinical Research, Pharmacovigilance, Pharmaceutical Sciences, Pharmaceutics, Clinical Documentation, Regulatory Compliance, Drug Safety, Biotechnology, Pharmaceutical Regulatory Affairs, eCTD Publishing, Pharmaceutical Quality Systems
Experience Required
- 2–3+ Years of Medical Writing Experience
Candidates with experience in pharmaceutical companies, CROs, or regulatory consulting firms are preferred.
Required Skills
Candidates applying for this Medical Writing role should possess:
- Strong regulatory and clinical writing skills
- Experience with CTD and eCTD submissions
- Knowledge of ICH E2, E3, E6, and M4 guidelines
- Understanding of EMA and MHRA regulations
- Experience in aggregate safety report preparation
- Scientific writing and editing expertise
- Strong data interpretation skills
- Documentation management system knowledge
- Excellent communication and stakeholder coordination abilities
- Ability to manage multiple regulatory projects
Professionals with exposure to global pharmaceutical regulatory systems may receive preference.
Why Medical Writing Is a High-Demand Pharma Career
Medical Writing has become one of the fastest-growing pharmaceutical career domains due to increasing regulatory requirements, clinical trial documentation needs, and global drug approval processes.
Medical Writing professionals support:
- Drug development programs
- Regulatory submissions
- Clinical trial documentation
- Pharmacovigilance reporting
- Aggregate safety reporting
- Global regulatory compliance
- eCTD publishing systems
- Scientific communication
Growing pharmaceutical outsourcing and global clinical development programs have significantly increased demand for experienced medical writers.
Professionals working in Regulatory Medical Writing gain opportunities in:
- Pharmaceutical companies
- CROs
- Pharmacovigilance organizations
- Regulatory consulting firms
- Clinical research organizations
- Global healthcare companies
Location & Salary
Job Location
Miyapur, Hyderabad
Work Mode
- Full-Time
- Work From Office
- No Work From Home
Expected Salary
Based on current pharmaceutical industry salary trends in Hyderabad, approximate salary ranges may include:
- Medical Writer: ₹5 LPA to ₹8 LPA
- Senior Medical Writer: ₹8 LPA to ₹12 LPA
- Regulatory Medical Writer: ₹7 LPA to ₹14 LPA
Salary may vary depending on:
- Regulatory writing expertise
- CTD/eCTD experience
- Pharmacovigilance documentation exposure
- Clinical writing experience
- Global regulatory project exposure
Immediate joiners may receive preference during the recruitment process.
Application Process
Interested candidates can apply by sharing their PDF CV through email.
Email ID
Subject Line
Senior Medical Writer / Regulatory Medical Writer
Official Website
Candidates should include:
- Total experience
- Current CTC
- Expected CTC
- Notice period
- Medical writing experience
- CTD/eCTD submission exposure
- Pharmacovigilance documentation experience
Frequently Asked Questions (FAQs)
Which company is hiring Medical Writers in Hyderabad?
Masuu Global Solutions is hiring Senior Medical Writer and Regulatory Medical Writer professionals in Hyderabad.
What qualifications are eligible for this role?
Candidates with B.Pharm, M.Pharm, Life Sciences, Biotechnology, Medicine, or related healthcare qualifications are eligible.
What experience is required?
Candidates should have 2–3+ years of Medical Writing experience.
What skills are preferred for this position?
Candidates with CTD/eCTD documentation, clinical writing, pharmacovigilance reporting, and ICH guideline knowledge are preferred.
Is this a work-from-home role?
No. This is a full-time work-from-office role in Hyderabad.
How can candidates apply?
Interested candidates can send their PDF CV to hiring@masuuglobal.com.
Summary Table
| Company | Masuu Global Solutions |
|---|---|
| Department Vacancies | Senior Medical Writer, Regulatory Medical Writer |
| Qualification | B.Pharm, M.Pharm, Life Sciences, Biotechnology, Medicine |
| Experience | 2–3+ Years |
| Location | Miyapur, Hyderabad |
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