Konovo Pharmacovigilance Manager
- Konovo Hiring Pharmacovigilance Manager in Bangalore | PV & Drug Safety Leadership Role
- Company Overview
- Job Role & Responsibilities
- Patient Safety & Compliance
- Data Quality & Reporting
- Process Development & SOP Management
- Cross-Functional Collaboration
- Leadership & Decision Making
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is the main responsibility?
- 3. What career growth can I expect?
- 4. Is leadership experience required?
- Summary
Konovo Hiring Pharmacovigilance Manager in Bangalore | PV & Drug Safety Leadership Role
A senior-level opportunity is now open for experienced pharmacovigilance professionals looking to move into leadership and strategic roles. Konovo is hiring a Pharmacovigilance Manager in Bangalore to lead patient safety, compliance, and data quality operations across global healthcare research programs.
This role is ideal for candidates with 5–7 years of experience in pharmacovigilance, drug safety, or regulatory compliance who want to work in a fast-growing healthcare intelligence company with global exposure.
Company Overview
Konovo is a global healthcare intelligence company focused on transforming research through advanced technology and data-driven insights. With access to over 2 million healthcare professionals worldwide, Konovo supports leading pharmaceutical companies, medical device firms, and research organizations.
Operating across multiple countries including India, the UK, the US, and Europe, Konovo is evolving into a product-driven platform that integrates data, technology, and patient safety compliance to accelerate healthcare innovation.
Job Role & Responsibilities
As a Pharmacovigilance Manager, you will lead patient safety operations, ensure regulatory compliance, and manage adverse event reporting processes across global research studies.
Patient Safety & Compliance
- Oversee adverse event (AE), serious adverse event (SAE), and product complaint reporting
- Ensure compliance with global pharmacovigilance regulations and client requirements
- Collaborate with internal teams and client safety departments to evaluate safety cases
- Maintain accurate tracking and documentation of safety data
Data Quality & Reporting
- Manage quality control processes for research data and safety reporting
- Conduct validation checks to ensure accuracy and compliance
- Ensure timely reporting of safety data to stakeholders and regulatory teams
Process Development & SOP Management
- Develop and implement SOPs for pharmacovigilance and data quality workflows
- Manage training programs related to patient safety and compliance
- Ensure documentation meets audit and regulatory standards
Cross-Functional Collaboration
- Work with operations, product, and engineering teams to improve systems
- Drive innovation in safety data management and reporting tools
- Support continuous improvement initiatives across the organization
Leadership & Decision Making
- Lead quality and compliance initiatives across teams
- Mentor team members and improve operational efficiency
- Make strategic decisions related to compliance risks and process improvements
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, Pharm.D, MSc Life Sciences, Biotechnology, Clinical Research
Experience Required:
- 5–7 years of experience in pharmacovigilance, drug safety, or regulatory compliance
- Experience in adverse event reporting and safety data management
Skills Required:
- Strong knowledge of global pharmacovigilance regulations and guidelines
- Experience in quality control and compliance processes
- Leadership and team management skills
- Strong analytical and decision-making abilities
- Excellent communication and stakeholder management skills
- Experience with data systems, reporting tools, and safety databases
Location & Salary
- Location: Bangalore, India
- Work Mode: Hybrid
- Job Type: Full-time
- Salary: Competitive package with performance-based benefits
Application Process
Interested candidates can apply through the official careers portal:
Apply Here: https://job-boards.greenhouse.io/konovo/jobs/5138569008
Early application is recommended due to high competition for senior pharmacovigilance roles.
Why This Role Matters in Healthcare
Pharmacovigilance managers play a critical role in ensuring drug safety and regulatory compliance. Their work directly impacts patient safety, risk management, and the successful delivery of healthcare innovations to the market.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, this is a senior-level role requiring 5–7 years of experience.
2. What is the main responsibility?
Managing pharmacovigilance operations, compliance, and safety data reporting.
3. What career growth can I expect?
You can grow into roles like PV Director, Safety Lead, or Regulatory Strategy Head.
4. Is leadership experience required?
Yes, candidates should have experience in managing teams or processes.
Summary
| Category | Details |
|---|---|
| Company | Konovo |
| Vacancies | Pharmacovigilance Manager |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, MSc |
| Experience | 5–7 Years |
To apply for this job please visit job-boards.greenhouse.io.
