Veeda Lifescience Hiring Fresher for Medical Writer Role
Veeda Lifescience, a global clinical research organization, is hiring for the role of Medical Writer at its Ahmedabad location. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to build a career in medical writing, scientific documentation, and clinical research communication.
The role focuses on supporting clinical documents, regulatory‑related content, scientific reports, and medical communication deliverables within a structured and quality‑driven environment. Candidates will work closely with cross‑functional teams to ensure accurate, compliant, and well‑structured medical content.
🏢 About Veeda Lifescience
Veeda Lifescience is a globally recognized organization providing clinical research, regulatory, and data services to pharmaceutical and biotechnology companies. The company follows strict regulatory and quality standards and supports drug development activities across multiple therapeutic areas. Working at Veeda Lifescience allows freshers to gain structured exposure to clinical research documentation and regulatory‑aligned writing practices.
📊 Job Details
- Position: Medical Writer
- Department: Medical writing
- Location: Ahmedabad
- Experience: 0 to 2 Years
- Qualification: B.Pharm, M.Pharm
- Job Type: Full-Time
- Last Date of application: Not provided
📋 Key Functions – Medical Writer
- Prepare and review clinical study documents including Protocols, Informed Consent Documents (ICD), Study Synopses, and other study‑specific materials such as patient diary cards.
- Prepare and review Investigator Brochures in accordance with regulatory and sponsor requirements.
- Support preliminary and detailed trial feasibility assessments for patient‑based clinical studies in coordination with the medical team for regulatory submissions.
- Perform reference literature searches and reviews to support assigned clinical and regulatory projects.
- Provide protocol training to monitors and site teams as required.
- Prepare and review Clinical Study Reports (CSRs) for various trial phases conducted by the Clinical Operations team.
- Define CSR timelines in the project execution grid in coordination with the Project Manager.
- Prepare and review full CSRs, abbreviated CSRs, synoptic CSRs, CSR shells, and interim reports as per sponsor requirements.
- Finalize CSRs and related appendices for submission as part of CTD/eCTD dossiers, ensuring regulatory compliance.
- Review Statistical Analysis Plans (SAPs), mock shells, and Table/Figure/Listing (TFL) specifications for content accuracy and consistency.
- Audit & Inspection Readiness: Support sponsor audits and regulatory inspections (e.g., US FDA, EMA, DCGI) and prepare responses to queries or deficiencies.
🎓 Eligibility Requirements
- Educational Qualification
- Degree in Life Sciences or related healthcare disciplines.
- Required qualifications include B.Pharmacy or M.Pharmacy.
- Experience
- Experience in medical writing, clinical research, or regulatory documentation is preferred.
- Freshers with strong scientific writing skills and sound clinical knowledge may also be considered.
- Scientific Writing & Editing: Strong ability to write, edit, and review scientific and clinical documents with clarity and accuracy.
- Clinical & Regulatory Knowledge
- Good understanding of clinical trial processes, Clinical Study Reports (CSRs), and regulatory submission requirements.
- Familiarity with ICH guidelines and global regulatory standards.
🧠 Skill Set Required
- High level of accuracy and consistency in document preparation and review.
- Effective communication skills with the ability to collaborate across cross‑functional clinical and regulatory teams.
- Ability to understand and organize scientific information
- Willingness to learn regulatory and documentation standards
- Working knowledge of MS Word and basic MS Office tools
⭐ Role Breakdown
The Medical Writer role is a highly sought‑after career path in clinical research and regulatory domains. For freshers, this position offers an excellent entry point to learn how scientific and clinical information is transformed into structured, compliant documents. Exposure to real‑world clinical documentation at Veeda Lifescience helps build strong foundations for long‑term growth in medical writing and regulatory communication.
🎯 Suitable Applicants
This opportunity is suitable for:
- Fresh pharmacy or life sciences graduates
- Candidates interested in medical writing careers
- Freshers with good scientific understanding and writing skills
- Individuals seeking entry‑level roles in clinical research documentation
📈 Career Progression
With experience and continuous learning, Medical Writers can progress into roles such as:
- Senior Medical Writer
- Regulatory Medical Writer
- Clinical Documentation Specialist
- Medical Writing Lead
Veeda Lifescience also provides exposure to diverse projects and learning opportunities.
💰 Expected Pay
- The expected salary range for this role typically depends on experience level, skill set, and company policies.
- Candidates can expect a competitive salary package based on their background and performance during the selection process.
💡 Application Tips
- Highlight writing skills and subject knowledge in your resume
- Practice writing clear and concise scientific content
- Revise basic clinical research and medical terminology
- Learn common clinical document types
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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FAQ – Medical Writer
1. Who can apply for the Medical Writer role at Veeda Lifescience?
Candidates with a B.Pharmacy or M.Pharmacy degree in Life Sciences or related healthcare disciplines can apply.
2. Is this role suitable for freshers?
Yes. Freshers with strong scientific writing skills and good clinical knowledge are encouraged to apply. Candidates with up to 2 years of experience in medical writing or clinical research are also suitable.
3. What type of documents will I work on in this role?
You will work on Protocols, Informed Consent Documents (ICDs), Investigator Brochures, Clinical Study Reports (CSRs), summaries, and other regulatory‑related clinical documents.
4. Will I be involved in Clinical Study Report (CSR) writing?
Yes. The role includes preparation and review of Full CSRs, Abbreviated CSRs, Synoptic CSRs, interim reports, shells, and related appendices.
5. Does the role involve regulatory submission support?
Yes. You will contribute to CTD/eCTD submission documents, ensuring compliance with ICH guidelines and global regulatory requirements.
