Current jobs related to Pharmacovigilance Manager - Bengaluru, Karnataka - Novaspire Biosciences

  • Data Quality Analyst

    2 weeks ago

    Bengaluru, Karnataka, India beBeeDataQuality Full time ₹ 25,00,000 - ₹ 45,00,000

    Job Title: Data Quality Analyst - PharmacovigilanceAs a data quality analyst in pharmacovigilance, you will be responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global regulations.Key ResponsibilitiesData entry, seriousness assessment, and causality assessment of adverse event reports in the PV...

  • Pharmacovigilance Scientist

    2 weeks ago

    Bengaluru, Karnataka, India Propharma Group Full time US$ 90,000 - US$ 1,20,000 per year

    The Pharmacovigilance (PV) Scientist supports the activities in the Benefit Risk group by ensuring that day-to-day operational activities are completed. The PV Safety Scientist is expected to be professional and diligent and liaise with the director and management group members within the team on any issues, as well as coordinate the work with the senior PV...

  • PV Professional

    7 days ago

    Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 5,00,000 - ₹ 8,00,000

    PV Specialist Role We are seeking a skilled PV Specialist to join our team. As a key member, you will play a pivotal role in ensuring the high-quality execution of pharmacovigilance processes. Key Responsibilities: Literature Review: Design and implement comprehensive search strategies using databases such as Embase, Medline, PubMed, and Ovid to ensure...

  • Senior Pharmacovigilance Specialist

    5 days ago

    Bengaluru, Karnataka, India Clarivate Full time

    Senior Pharmacovigilance SpecialistJob Profile SummaryThis position involves Biomedical Literature Searching in our team and requires knowledge of biomedical literature and searching databases such as MEDLINE Embase and Biosis Previews You will need broad knowledge of biomedical terminology drugs and therapeutic areas In this role you are responsible...

  • Analyst - Pharmacovigilance

    2 weeks ago

    Bengaluru, Karnataka, India Elanco Full time

    Job DescriptionAt Elanco (NYSE: ELAN) - it all starts with animalsAs a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals,...

  • Pharmacovigilance Specialist, Case Processing

    2 weeks ago

    Bengaluru, Karnataka, India Propharma Group Full time US$ 90,000 - US$ 1,20,000 per year

    Job DescriptionThe Pharmacovigilance (PV) Specialist, Case Processing manages individual case safety reports, performs initial case-level assessment of expectedness, confirms seriousness, composes accurate and thorough medical narratives, and generates queries for missing or unclear information. The PV Specialist ensures all cases meeting expedited...

  • Safety and Compliance Specialist

    2 weeks ago

    Bengaluru, Karnataka, India beBeeRegulatory Full time US$ 1,20,000 - US$ 1,40,000

    Pharmacovigilance Professional OpportunityWe are seeking an experienced Pharmacovigilance Manager to join our team at Novaspire Biosciences. The ideal candidate will have a strong background in pharmacovigilance and excellent organizational skills.Main Responsibilities:Organize, manage, and maintain a highly compliant PV system.Maintain awareness and ensure...

  • Medicines Safety Expert

    1 week ago

    Bengaluru, Karnataka, India beBeePharmacovigilance Full time

    Job Title: Pharmacovigilance Lead", "Manage a comprehensive medical review process for adverse event reports to ensure accuracy, relevance, and consistency with supporting documents.Evaluate the seriousness and coding of adverse events, and provide causality assessments to support medical sign off.Rectify coding errors in medical history, lab details, or...

  • Data Specialist

    2 weeks ago

    Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 9,00,000 - ₹ 13,55,000

    Job TitleWe are seeking a Data Officer to contribute to pharmacovigilance activities and work effectively within a team.The ideal candidate will perform local safety case receipt, processing, data entry, quality control (QC) tracking, and ICSR follow-up for clients, adhering to agreed timelines.Manage email boxes as required.Register, triage, assign, and...

  • Medical Reviewer/Drug Safety Physician

    2 weeks ago

    Bengaluru, Karnataka, India Propharma Group Full time US$ 90,000 - US$ 1,20,000 per year

    The PV Drug Safety Physician should be able to perform medical review of all types of individual case safety reports (ICSRs) by writing an expert company pharmacovigilance comment. The PV Drug Safety Physician maintains distinctive quality and commitment as the operating philosophy in carrying out all processes., and continually seeks out ways to enhance...

Pharmacovigilance Manager

2 weeks ago

Bengaluru, Karnataka, India Novaspire Biosciences Full time

Company Description

At Novaspire Biosciences, we pride ourselves on being a trusted partner to the pharmaceutical industry, delivering comprehensive, high-quality clinical research services. We specialize in supporting pharmaceutical, biotechnology, medical device, and nutraceutical companies at every stage of the drug/product development lifecycle, from clinical studies Phase I to post-market surveillance. Our core services include pharmacovigilance, clinical trials, medical writing, bioequivalence study support, GxP consulting services & training, and imaging studies. With over 75 years of combined experience, our team provides solutions and streamlined processes to ensure efficient and effective research outcomes.

Role Description


• Organize, manage and maintain a highly compliant Pharmacovigilance (PV) system


• Maintain awareness and ensure adherence to established and updated local and global processes and guidelines as well as national and international regulations and guidelines for pharmacovigilance.


• Ensure PV business continuity and after hours availability.


• Lead and coordinate internal and external PV audits and inspections.


• Monitor PV system performance and compliance of partners and distributors.


• Maintain expertise in country as well as worldwide regulations and guidelines and promote increased awareness of the legislative and regulatory environment in the country.


• Accountable for all strategic PV activities


• Active contribution to the activities relevant to the pharmacovigilance system to ensure monitoring of the safety profile


• Act as the responsible contact person in the region, internally and externally, for safety-related aspects and PV.


• Ensure internal regulatory/PV processes and procedures are well documented and support compliant regulatory/PV activities.


• Perform other duties as assigned.

Skills Required:


• In depth knowledge of national/regional regulatory legislation and guidelines.


• Knowledge of the pharmacovigilance regulations of all the countries.


• Demonstrated ability to provide quality work using strong organizational, facilitation and interpersonal skills in a cross-functional team locally, within PV and externally.


• Skilled at people management including overseeing and controlling outsourced vendor activities in a compliance/regulated field.


• Capable of troubleshooting and managing multiple projects simultaneously.


• Strong knowledge and understanding of medical terminology and clinical development processes


• Rational approach to issues and their business implications, good problem solving and decision making skills.


• Highly analytical with the ability to give attention to detail.


• Excellent organizational skills and capable of working efficiently.


• Possess an excellent interpersonal, verbal, and written communication skills. 

Minimum Requirements:


• Minimum five years of working experience within the pharmaceutical industry and minimum five years within pharmacovigilance.


• Degree / Advanced degree in medicine or in life sciences or equivalent experience


• Excellent communication skills including proficiency in verbal and written English


• Experience in other affiliate medical functions (e.g., Medical Affairs, Clinical Operations, Medical Information) or global clinical product development is considered advantageous.


• Proficiency in Microsoft Word and Excel.