Veeda Lifesciences Hiring Medical Writer

Veeda Lifesciences Hiring Medical Writer – Clinical Research Role | Ahmedabad Hybrid Opportunity

Veeda Lifesciences is hiring Medical Writer professionals for its clinical research and regulatory documentation team in Ahmedabad, Gujarat. This is a full-time hybrid opportunity for candidates with experience or strong knowledge in medical writing, clinical trials documentation, and regulatory submissions. The role focuses on preparing clinical study reports, protocols, and regulatory documents essential for drug development and approvals.

Company Overview

Veeda Lifesciences is a leading contract research organization (CRO) in India, specializing in clinical trials, bioequivalence studies, and regulatory consulting services. The company works with global pharmaceutical and biotechnology clients to support drug development, clinical research, and regulatory submissions across international markets.

With strong expertise in clinical pharmacology, data management, and medical writing, Veeda Lifesciences is recognized for delivering high-quality, compliant, and scientifically robust clinical documentation aligned with global standards such as USFDA, EMA, and DCGI.

Job Role & Responsibilities

As a Medical Writer, you will be responsible for preparing and reviewing high-quality clinical and regulatory documents that support clinical trials and drug approval processes. This role requires strong scientific writing skills, attention to detail, and knowledge of regulatory guidelines.

Clinical Documentation & Writing

• Prepare and review clinical trial documents including protocols, informed consent documents (ICD), and study synopses
• Develop investigator brochures and patient-facing materials such as diary cards
• Write and finalize Clinical Study Reports (CSRs), including full CSR, abbreviated CSR, interim reports, and synoptic summaries
• Ensure all documents meet regulatory requirements for CTD/eCTD submissions

Regulatory & Scientific Support

• Conduct literature searches and reviews to support clinical documentation and regulatory submissions
• Evaluate trial feasibility in collaboration with medical and clinical teams
• Review statistical analysis plans, tables, figures, and listings for accuracy and completeness
• Support responses to regulatory queries and audits from authorities such as USFDA, EMA, and DCGI

Quality & Compliance

• Ensure all clinical documents comply with internal SOPs and global regulatory standards
• Maintain high-quality writing, editing, and formatting standards
• Archive and manage clinical documents in compliance with regulatory guidelines

Process Improvement & Training

• Develop templates, formats, and documentation standards for clinical writing
• Provide protocol training to clinical teams and site staff when required
• Participate in process improvement initiatives and training programs

Eligibility / Qualifications

Educational Qualification

Candidates must have a degree in Life Sciences or related healthcare disciplines.

Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research

Experience

• Experience in medical writing, clinical research, or regulatory documentation is preferred
• Freshers with strong writing skills and clinical knowledge may also be considered

Skills Required

• Strong scientific writing and editing skills
• Knowledge of clinical trials, CSRs, and regulatory submission processes
• Familiarity with ICH guidelines and global regulatory requirements
• Attention to detail and document accuracy
• Good communication and collaboration skills

Location & Salary

• Job Location: Ahmedabad, Gujarat, India
• Work Mode: Hybrid
• Employment Type: Full-time
• Salary: Competitive salary based on experience and industry standards in medical writing and clinical research

Application Process

Interested candidates can apply through the official job posting link below:

Apply Here: https://www.linkedin.com/jobs/view/4389551867

Why This Role Matters in Healthcare

Medical writers play a crucial role in translating complex clinical data into clear, regulatory-compliant documents that support drug approvals and patient safety. This role directly contributes to bringing safe and effective medicines to market by ensuring accurate and transparent clinical reporting.

Frequently Asked Questions (FAQs)

1. Who can apply for this role?

Candidates with Life Sciences, Pharmacy, Biotechnology, or Clinical Research backgrounds can apply.

2. Is experience mandatory?

Experience is preferred, but candidates with strong medical writing skills and clinical knowledge may also be considered.

3. What documents will I work on?

You will work on protocols, CSRs, investigator brochures, regulatory submissions, and clinical study documentation.

4. What is the career growth in medical writing?

You can progress to Senior Medical Writer, Regulatory Writer, or Clinical Documentation Lead roles.

5. Is this a good pharma career option?

Yes. Medical writing is a high-demand, high-growth career in clinical research and regulatory affairs.

Summary Table

Category	Details
Company	Veeda Lifesciences
Vacancies	Medical Writer
Required Education	B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research
Experience	Preferred (Freshers May Apply)

Tagged as: Pharma Jobs in Ahmedabad