Jeevan Scientific Hiring Senior Medical Writer

Meta Title: M.Pharm Medical Writer Jobs Hyderabad CRO

Meta Description: B.Pharm, M.Pharm, PhD candidates apply for Senior Medical Writer role at Jeevan Scientific Hyderabad. 5–8 yrs exp.

Jeevan Scientific Technology Ltd., a leading CRO company, is hiring experienced professionals for Senior Medical Writer – Report Writing roles at its Hyderabad location. This is a high-value opportunity for candidates looking for medical writing jobs, clinical research careers, regulatory writing roles, and CRO industry opportunities. Professionals with expertise in Clinical Study Reports (CSR), protocol writing, and eCTD submissions can build strong long-term careers in regulatory affairs and pharmaceutical clinical documentation.

Company Overview

Jeevan Scientific Technology Ltd. is a recognized Contract Research Organization (CRO) providing clinical research, regulatory, and pharmacovigilance solutions to the pharmaceutical and healthcare industries. The company works closely with regulatory standards and clinical trial processes, making it a strong platform for professionals seeking careers in medical writing, clinical documentation, and regulatory submissions.

The CRO industry plays a critical role in accelerating drug development, ensuring clinical compliance, and supporting global healthcare innovation. Working in a CRO environment provides exposure to international regulatory guidelines, clinical trial documentation standards, and pharmaceutical research operations.

Professionals working in medical writing and regulatory documentation contribute directly to the approval and commercialization of healthcare products.

Job Role & Responsibilities

Jeevan Scientific is hiring for the role of Senior Medical Writer – Report Writing with designation levels including Assistant Manager and Deputy Manager.

Core Responsibilities

• Prepare and review Clinical Study Reports (CSR) for BA/BE studies and clinical trials
• Develop medical writing documents including protocol writing and study synopsis preparation
• Prepare summary tables including DBE tables, BTIF, and regulatory submission documents
• Compile and publish regulatory submissions in eCTD format
• Collect and review literature data for study documentation
• Coordinate with ethics committees and ensure regulatory compliance
• Ensure accuracy, consistency, and compliance with ICH-GCP and global regulatory guidelines

These responsibilities are critical in supporting clinical research documentation, regulatory approvals, and pharmaceutical product development.

Eligibility / Qualifications

• Qualification: B.Pharm, M.Pharm, M.Pharm PhD
• Experience: 5 to 8+ years
• Industry Preference: CRO industry experience mandatory

Relevant Courses

B.Pharm, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Pharm Pharmacology, PhD in Pharmacy, Clinical Research Courses, Regulatory Affairs Certification

Required Skills

• Clinical Study Report (CSR) writing
• Medical writing and protocol writing expertise
• eCTD submission and regulatory documentation knowledge
• Understanding of BA/BE studies and clinical trials
• Knowledge of ICH-GCP and regulatory guidelines
• Literature review and study synopsis preparation
• Ethics committee coordination and compliance management

Location & Salary

Job Location: Hyderabad

Salary: As per company standards (competitive CRO medical writing salary package based on experience and expertise)

Medical writing and regulatory affairs roles are among the highest-paying domains in clinical research due to their technical and regulatory importance.

Application Process

Interested candidates meeting the above requirements can share their updated CV to:

Email: sharad.chandra@jeevanscientific.com

Immediate joiners will be preferred.

Candidates should ensure that their resume clearly highlights experience in CSR writing, protocol development, eCTD submissions, and CRO regulatory documentation.

Why This Opportunity Matters

Medical writing is one of the fastest-growing and highest-value career domains in the pharmaceutical and clinical research industry. Regulatory agencies require detailed, accurate, and compliant documentation for drug approvals, making experienced medical writers highly valuable.

Professionals with expertise in CSR writing, protocol preparation, and eCTD publishing are in strong demand across CROs, pharmaceutical companies, and global clinical research organizations.

Working in this domain not only improves technical expertise but also provides opportunities for international projects, remote work options, and high-paying regulatory affairs careers.

Key Highlights

• Company: Jeevan Scientific Technology Ltd.
• Industry: CRO / Clinical Research
• Role: Senior Medical Writer – Report Writing
• Designation: Assistant Manager / Deputy Manager
• Qualification: B.Pharm, M.Pharm, PhD
• Experience: 5–8+ Years
• Location: Hyderabad

FAQs

Who can apply for this medical writing role?

Candidates with B.Pharm, M.Pharm, or PhD qualifications and relevant CRO experience can apply.

Is CRO experience mandatory?

Yes, candidates must have prior experience working in the CRO industry.

What skills are required?

Medical writing, CSR preparation, protocol writing, eCTD submissions, and regulatory documentation.

What is the preferred experience?

5 to 8+ years in medical writing or clinical research documentation.

How can I apply?

You can apply by sending your updated CV to the official HR email ID.

Summary Table

|———————————-|———————————-|
| Company | Jeevan Scientific Technology Ltd. |
| Vacancies | Senior Medical Writer (Asst. Manager / Dy. Manager) |
| Required Education | B.Pharm, M.Pharm, PhD |

Experience	5–8+ Years