Vizen Life Sciences Hiring Drug Safety Associate & Drug Safety Physician | Pharmacovigilance Jobs
- Vizen Life Sciences Hiring Drug Safety Associate & Drug Safety Physician | Pharmacovigilance Jobs | Immediate Joiners
- Company Overview
- Job Role & Responsibilities
- Drug Safety Associate (2–8 Years Experience)
- Drug Safety Physician (MBBS/BDS)
- Eligibility / Qualifications
- Drug Safety Associate
- Drug Safety Physician
- Key Skills Required
- Location & Employment Details
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is pharmacovigilance experience mandatory?
- 2. Are freshers eligible?
- 3. What qualifications are required for the Drug Safety Physician role?
- 4. What experience range is required for Drug Safety Associate?
- 5. Are immediate joiners preferred?
- Summary
Vizen Life Sciences Hiring Drug Safety Associate & Drug Safety Physician | Pharmacovigilance Jobs | Immediate Joiners
Vizen Life Sciences is currently hiring for multiple positions in its Pharmacovigilance and Drug Safety department. The open roles include Drug Safety Associate (2–8 years experience) and Drug Safety Physician (MBBS/BDS qualified). These positions are ideal for professionals with mandatory pharmacovigilance experience who are ready to join immediately and contribute to global drug safety operations.
As regulatory scrutiny around drug safety, adverse event reporting, and risk management continues to increase globally, experienced pharmacovigilance professionals are in strong demand. These roles provide exposure to safety data management, medical review, signal detection, and regulatory compliance aligned with international health authority standards.
Company Overview
Vizen Life Sciences operates in the life sciences and healthcare services domain, supporting pharmaceutical, biotechnology, and medical device companies in ensuring regulatory compliance and patient safety. The organization focuses on pharmacovigilance, drug safety monitoring, regulatory documentation, and risk management services.
Drug safety functions are critical in protecting patient health and maintaining compliance with global regulatory authorities such as the US FDA, EMA, MHRA, and other international agencies. Through structured safety reporting systems and medical evaluation processes, Vizen Life Sciences contributes to strengthening post-marketing surveillance and risk mitigation strategies for marketed and investigational products.
Professionals joining the organization gain hands-on exposure to global safety databases, aggregate reporting, regulatory timelines, and quality-driven pharmacovigilance systems.
Job Role & Responsibilities
Drug Safety Associate (2–8 Years Experience)
The Drug Safety Associate will be responsible for managing day-to-day pharmacovigilance activities and ensuring compliance with global drug safety regulations.
Key Responsibilities:
- Processing and reviewing Individual Case Safety Reports (ICSRs).
- Performing case triage, data entry, coding (MedDRA/WHO-DD), and medical assessment support.
- Conducting follow-ups for incomplete safety information.
- Supporting aggregate report preparation where applicable.
- Ensuring compliance with global pharmacovigilance regulations and client SOPs.
- Maintaining accurate documentation within safety databases.
- Supporting audit and inspection readiness.
Candidates must have hands-on pharmacovigilance experience and strong understanding of adverse event reporting workflows.
Drug Safety Physician (MBBS/BDS)
The Drug Safety Physician will play a critical role in medical review, signal detection, and benefit-risk evaluation activities.
Key Responsibilities:
- Medical review and assessment of Individual Case Safety Reports.
- Causality assessment and narrative writing.
- Evaluation of serious adverse events and medically significant cases.
- Contribution to signal detection and risk management activities.
- Supporting aggregate safety report review (PSUR, PBRER, DSUR, etc.).
- Providing medical input for regulatory submissions and health authority responses.
- Ensuring compliance with ICH guidelines and global pharmacovigilance standards.
This position requires strong clinical judgment, analytical thinking, and regulatory awareness.
Eligibility / Qualifications
Drug Safety Associate
Educational Qualification:
B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MSc Pharmacology, MSc Biotechnology, or related healthcare qualification.
Experience:
- 2–8 years of pharmacovigilance experience.
- Experience in ICSR processing and safety database management.
- Understanding of global regulatory reporting requirements.
Drug Safety Physician
Educational Qualification:
MBBS, BDS (Completed and registered).
Experience:
- Pharmacovigilance experience is mandatory.
- Experience in medical review, case assessment, and regulatory safety documentation preferred.
Key Skills Required
- Strong knowledge of pharmacovigilance processes and global safety regulations.
- Familiarity with ICH guidelines and adverse event reporting standards.
- Attention to detail and high-quality documentation practices.
- Ability to manage timelines and multiple case workflows.
- Strong communication and analytical skills.
- Experience working with safety databases and regulatory compliance systems.
Location & Employment Details
- Employment Type: Full-time
- Joining: Immediate joiners preferred
- Department: Pharmacovigilance / Drug Safety
Salary details are not disclosed publicly. Compensation is aligned with industry standards for drug safety and pharmacovigilance professionals based on experience and qualification.
Application Process
Interested and eligible candidates can submit their updated CV to:
Email: careers@vizenlifesciences.com
Applicants are advised to clearly mention the position applied for (Drug Safety Associate or Drug Safety Physician) in the subject line of the email and highlight relevant pharmacovigilance experience.
Frequently Asked Questions (FAQs)
1. Is pharmacovigilance experience mandatory?
Yes. Prior pharmacovigilance experience is mandatory for both roles.
2. Are freshers eligible?
No. Only candidates with relevant drug safety experience will be considered.
3. What qualifications are required for the Drug Safety Physician role?
Candidates must hold MBBS or BDS qualification with pharmacovigilance exposure.
4. What experience range is required for Drug Safety Associate?
Candidates with 2 to 8 years of pharmacovigilance experience are eligible.
5. Are immediate joiners preferred?
Yes. Immediate joiners will be given preference.
Summary
| Company | Vizen Life Sciences |
|---|---|
| Vacancies | Drug Safety Associate; Drug Safety Physician |
| Required Education | B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MBBS, BDS |
| Experience | 2–8 Years (Associate); PV Experience Mandatory (Physician) |
To apply for this job email your details to careers@vizenlifesciences.com
