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Vigilare Biopharma Jobs: Pharmacovigilance, Regulatory Affairs & Medical Writing
Published on: October 29, 2026
Vigilare Biopharma has listed three opportunities in Pharmacovigilance, Regulatory Affairs and Medical Writing. These positions focus on drug safety, regulatory submissions and clinical documentation, with experience requirements varying by role.
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1. Pharmacovigilance (PV) Associate / Scientist
This position focuses on drug safety case processing, quality checks and safety reporting.
Job Details
| Job Detail | Information |
|---|---|
| Company | Vigilare Biopharma |
| Job Role | Pharmacovigilance (PV) Associate / Scientist |
| Experience | 2–4 years |
| Employment Type | Full-time |
| Location | Hyderabad, India |
| Work Mode | Hybrid |
| Application | Apply Now |
Key Responsibilities
- Process and quality-check Individual Case Safety Reports (ICSRs).
- Perform MedDRA coding and prepare case narratives.
- Support expedited safety reporting and literature screening.
- Assist with PSUR and PBRER preparation.
Who should apply? Candidates with relevant Pharmacovigilance or Drug Safety experience, particularly in ICSR processing, coding and safety reporting.
2. Regulatory Affairs Specialist (eCTD & Submissions)
This role involves preparing and managing regulatory submissions and supporting regulatory lifecycle activities.
Job Details
| Job Detail | Information |
|---|---|
| Company | Vigilare Biopharma |
| Job Role | Regulatory Affairs Specialist (eCTD & Submissions) |
| Experience | 3–5 years |
| Employment Type | Full-time |
| Location | Hyderabad, India |
| Work Mode | Not specified |
| Application | Apply Now |
Key Responsibilities
- Compile, publish and track eCTD submission sequences.
- Support regulatory lifecycle changes.
- Prepare regulatory documents and assist with health authority queries.
- Coordinate with clients and internal teams.
Who should apply? Regulatory Affairs professionals with experience in eCTD publishing, submission management and regulatory documentation.
3. Medical Writer / Regulatory Documentation
This position involves preparing scientific documents for clinical research and regulatory purposes.
Job Details
| Job Detail | Information |
|---|---|
| Company | Vigilare Biopharma |
| Job Role | Medical Writer / Regulatory Documentation |
| Experience | 2+ years |
| Employment Type | Full-time |
| Location | Remote / Hybrid |
| Application | Apply Now |
Key Responsibilities
- Prepare clinical study protocols, clinical study reports and safety summaries.
- Follow applicable ICH and GCP requirements.
- Maintain document accuracy and consistency.
- Coordinate with scientific and regulatory teams.
Who should apply? Professionals with relevant medical writing or regulatory documentation experience and familiarity with clinical research documents.
4. How to Apply for Vigilare Biopharma Jobs
Interested candidates can visit the Vigilare Biopharma Careers page and select the relevant position to review the application instructions.
Prepare an updated CV highlighting your relevant experience, technical skills and previous work. Include a brief note explaining your suitability for the role. Review the eligibility criteria and follow the company’s instructions to submit your application.
Note: The company states that detailed job descriptions are shared during the screening process. Confirm the specific requirements for your preferred position before applying.
5. Important Notes for Applicants
- All three positions require prior experience and are not advertised as fresher vacancies.
- Specific educational qualifications and application deadlines are not provided in the available position summaries.
- Check the company’s careers page to confirm that the vacancy remains open before applying.
6. What to Highlight in Your CV
Before applying, take a moment to update your CV for the position you want. Employers are more likely to notice relevant skills and experience when they are clearly presented.
| Job Position | What to Highlight in Your CV |
|---|---|
| Pharmacovigilance (PV) Associate / Scientist | Experience with ICSR processing, MedDRA coding, case narratives and drug safety reporting |
| Regulatory Affairs Specialist | Hands-on experience with eCTD submissions, regulatory documentation and submission tracking |
| Medical Writer / Regulatory Documentation | Experience writing clinical documents, reviewing scientific content and working with ICH/GCP requirements |
You do not need to list every skill you have. Focus on the ones that match the role and, where possible, mention relevant projects or tasks you have handled. Be prepared to discuss the experience included in your CV during the interview.
7. Related Pharma Career Resources
8. Frequently Asked Questions
Are these positions suitable for freshers?
No. The listed experience requirements start at two years, so these roles are intended for experienced candidates.
Where are the jobs located?
The Pharmacovigilance and Regulatory Affairs positions are in Hyderabad, India. The Medical Writer position is listed as remote or hybrid.
What qualifications are required?
The available summaries do not specify exact degree requirements. Confirm the eligibility criteria with the company.
Where can I apply?
Use the Apply Now link in the relevant job table to visit the company’s careers page and review the application instructions.
Disclaimer: PharmaCareerUpdates.com is an independent job-information website and is not affiliated with Vigilare Biopharma. Vacancy details may change. Verify the current job status, eligibility and application instructions directly with the employer before applying.
