Pharmacovigilance Manager

Konovo is a global healthcare intelligence company on a mission to transform research through technology- enabling faster better connected insights.

Konovo provides healthcare organisations with access to over 2 million healthcare professionalsthe largest network of its kind globally. With a workforce of over 200 employees across 5 countries: India Bosnia and Herzegovina the United Kingdom Mexico and the United States we collaborate to support some of the most prominent names in healthcare. Our customers include over 300 global pharmaceutical companies medical device manufacturers research agencies and consultancy firms.

As we transition from a service-oriented model to a product-driven platform we are expanding our hybrid Bengaluru-based team. We are looking for a Pharmacovigilance Manager to contribute to our mission by overseeing all aspects of adverse event identification documentation and reporting across our market research studies.This position ensures all research activitiescomply withglobal marketresearch codes of conduct pharmacovigilance regulations and specific requirements of our clients.

HowYoull Make an Impact:

Lead Patient Safety &Compliance

• Ownand manageKonovospatient safety complianceprogram ensuring adverse events product complaints and special situations are reported accurately and on time in line with client contractual requirements

• Ensure market research protocols and study designs are executed in compliance with PV regulations and requirements to proactively avoid andidentifypotentialadverse events

• Partner closely with Client Services and internal/client-based patient safety teams to assess cases and determineappropriate actions

• Ensure patient safety case data is accurately captured tracked andmaintainedinKonovossystems

Drive Data Quality Excellence

• Manage resources within data quality managementto ensure research studies meet quality standards and support ongoing revenue recognition

• Prioritise assign and execute daily QC reviews across large volumes of survey datasets

• Apply rigorous validation checks while balancing speed accuracy and compliance

• Manage thetimelyandaccuratereporting of identifiedAEs/SAEs to clients PV departments and other stakeholders as needed adhering to strict client-specific timelines andregulatory requirements.

Build Scalable Processes

• Draft refine and implement SOPs and workflow documentation to scale patient safety and data quality operations

• Administer and support client-specific patient safety training programs with strong documentation and record-keeping

Collaborate & Innovate

• Work cross-functionally with Operations Product and Engineering teams to enhance tools and introduce innovative solutions

• Contribute to continuous improvement initiatives that strengthenKonovosposition as an industry leader in patient safety and data quality

Lead with Judgment

• Makeindependent decisions andfinalrecommendations that influence compliance strategy and operational outcomes

• Evaluate changing conditions assess risks and introducenew approachesto solve complex business challenges

What Were Looking For:

• You bring 57 years of experience in Pharmacovigilance compliance and data quality control ideally within the healthcare market research or adjacent regulated environments.
• You have hands-on experience identifying assessing and reporting adverse events with strong working knowledge of global PV regulations and client requirements
• You have experience in quality control and/or quality assurance with a track record of maintaining high standards at scale
• You have led or mentored others and know how to raise the bar on quality and accountability within a team
• You take ownership of outcomes not just tasks and follow through with precision in high-stakes compliance-driven work
• You are highly detail-oriented and consistently balance accuracy speed and sound judgement
• You are comfortable making decisions independently and know when to escalate based on risk and impact
• You are organised and able to prioritise effectively across competing deadlines and high volumes of work
• You collaborate well across functions and build trust with client services product and technical teams
• You communicate clearly and concisely especially when translating complex compliance requirements into action across global stakeholders
• You are comfortable working with data systems and evolving tools including AI-enabled workflows with strong judgement on data integrity and responsible use of technology
• You are energised by building and improving processes and look for ways to scale quality and compliance as the business grows
• You adapt quickly in a changing environment and approach ambiguity with structure and ownership
• Fluency in English with strong written and verbal communication skills required
• Proficiency in Microsoft Office Suite and experience working with data and reporting tools required

Why JoinKonovo

• Be part of a mission-driven organisation that is empowering life science researchers and data scientists with the broadest ecosystem of healthcare audiences and an intelligent AI-enabled platform so insights arent just collected theyre connected.

• Join a fast-growing global team with opportunities for professional growth and advancement.

• Enjoy a collaborative and hybrid work environment that fosters innovation and flexibility.

• Experience a workplace that puts employees first offering a workplace designed for growth well-being and balance.

• Become a part of an organisation that prioritises your well-being with comprehensive benefits including group medical coverage accident insurance and a robust leave policy. Our employee-centric policies ensure a rewarding and fulfilling work experience.

• Make a real-world impact by helping healthcare organisations innovate faster.

This is just the beginning of what we can accomplish together. Join us at Konovo and help shape the future of healthcare technology!

Apply now to be part of our journey.