Are you an M.Pharm or B.Pharm graduate with hands-on exposure to BA/BE or Phase I clinical studies? Hereβs an exciting opportunity to advance your career in Medical Writing with Veeda Clinical Research (Veeda CR), a well-established Contract Research Organization based in Ahmedabad, Gujarat. π
π Job Overview
- Position: Medical Writer (Associate Level)
- Company: Veeda Clinical Research
- Location: Ahmedabad, Gujarat
- Experience Required: BA/BE or Phase I clinical trial exposure
- Salary Range: βΉ5β8 LPA (Approx.)
- Employment Type: Full-Time, Permanent
- Openings: 1 Vacancy
This role is ideal for professionals who enjoy scientific documentation, regulatory compliance, and structured clinical writing.
π’ About Veeda Clinical Research
Veeda Clinical Research is a reputed Indian CRO specializing in:
- Bioequivalence (BA/BE) Studies
- Early-Phase (Phase I) Clinical Trials
- Regulatory Documentation & Support
The organization collaborates with global pharma and biotech companies while adhering to international standards such as ICH guidelines and CTD submission formats.
π― Key Responsibilities
π Protocol Preparation
- Drafting study protocols for BA/BE & Phase I trials
- Incorporating inputs from Investigators, QA/QC, Bioanalytical teams & Sponsors
- Preparing final versions for regulatory & ethics submissions
π Informed Consent Documents (ICD)
- Drafting ICDs in English
- Managing translation & back-translation
- Ensuring regulatory accuracy
π Clinical Study Documentation
- Preparing CRFs and study documents
- Supporting Clinical Study Report (CSR) drafting
- Ensuring compliance with ICH guidelines
π Literature Review & Scientific Support
- Conducting PK & safety literature surveys
- Supporting feasibility analysis
- Providing scientific inputs for submissions
π Regulatory Coordination
- Preparing regulatory submission documents
- Coordinating with Ethics Committees
- Collaborating with PIs & Clinical Investigators
β Internal Quality Control
- Performing QC checks
- Ensuring SOP & global compliance
π Eligibility Criteria
π Education
- M.Pharm (Any Specialization)
OR - B.Pharm (Pharmaceutical Analysis / QA / Pharmaceutics / Pharmacology)
πΌ Experience
- BA/BE or Phase I trial experience
- Exposure to medical writing & regulatory documentation
π Skills
- Strong medical writing & documentation
- Knowledge of CTD format
- Experience with CSR & protocol writing
- Understanding of ICH guidelines
π Why Choose Medical Writing?
Medical Writing is among the fastest-growing domains in pharma & clinical research. π
β Work on global clinical projects
β Exposure to international regulatory standards
β Competitive salaries
β Long-term career stability
β Career transition into Regulatory Affairs or Clinical Project Management
For pharmacy professionals who enjoy structured, analytical, and scientific communication, this field offers both intellectual depth and financial growth.
π Why Ahmedabad?
4
Ahmedabad is rapidly emerging as a pharmaceutical and CRO hub in India.
- Strong pharma & CRO ecosystem
- Growing clinical research infrastructure
- Affordable cost of living compared to Mumbai & Bangalore
- Excellent professional networking opportunities
π Who Should Apply?
This opportunity is ideal for:
- M.Pharm graduates with clinical documentation exposure
- BA/BE study center professionals
- Clinical Research Associates transitioning to documentation
- Pharmacovigilance professionals shifting to regulatory writing
π‘ Final Thoughts
The Medical Writer role at Veeda Clinical Research offers a strong foundation in clinical documentation, regulatory submissions, and international compliance standards.
For pharmacy graduates aiming to build a stable and growth-oriented career in clinical research, this opportunity in Ahmedabad is worth considering. π±
If you meet the eligibility criteria and are passionate about scientific writing and regulatory processes, take the next step in your pharma career journey today.
π Apply Now
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