Senior Manager – Medical Advisor, Medical services - Zuventus Healthcare Limited, A division of Emcure Pharmaceuticals - Regionally based
(2025-04)
- Preparation of drug appraisals
- Preparation of product monographs
- Preparation of training slides
- Preparation of Product FAQ's
- Prepare of product rationale
- Identifying place in therapy as and when required
- Provide strategic inputs for marketing plans during product launch
- CME slide set preparation
- Preparation of question set for panel discussion
- Attended advisory board meetings (Semaglutide)
- Conduct training sessions for Business officers
- Conducted training sessions for business officers – pan India (Semaglutide)
- Attended KOL's for field visit
- Review and approval of promotional literature (VA, LBL)
- Preparation of knock out points for organisational products
- Preparation of patient awareness literature
- Attending to Product Management Team for training regarding products and further discussion concerning identifying therapy gaps for existing products
- Attended liver Summit at Kolkata 2026 for semaglutide
- Conducted talk for physicians on ibutilde at Kokilaben Ambani hospital
Pharmacovigilance officer in-charge and Medical Advisor, Pharmacovigilance and medico-marketing - Franco-Indian Pharmaceuticals Private Limited - Regionally based
(2024-06)
- Drafting and submission of PSUR (periodic safety update reports)
- Conducting training sessions for medical representatives
- Updating and approving product labels
- Conducting lectures at product launch conferences
- Authoring drug monographs
- Attending to queries from consultants and physicians regarding organization's products
- Drafting and preparing slides and study articles for clinicians and specialist physicians for CME's
Medical Review Manager, Pharmacovigilance - Piramal Critical Care Limited - Regionally based, India
(2022-01 - 2024-06)
- Review and conduct medical assessment of pharmacovigilance / safety documents (ICSRs)
- Submission of veterinary cases in safety reporting portal
- Monitor adverse event reporting
- Support in medical information and product complaint activities for reports related to adverse events
- Support for internal or external/ regulatory audits and inspections
- Prepare and impart pharmacovigilance training
- Provide data for compliance of safety activities
- Review of literature articles (veterinary and human) for identification of ICSRs, safety and efficacy information for inclusion in aggregate reports, RMPs and signal reports
- Respond to queries and requests related to safety of products and the pharmacovigilance system from internal and external stakeholders including health authorities
- Conduct/ support drafting follow-up questionnaires to seek additional information from the reporter
- Reconciliation of queries with vendors
- Provide medical/clinical guidance to case processing and medical writing teams
- Preparation and review of procedural documents such as standard operating procedure (SOP), manual, etc
- Ensure compliance with all the company SOPs, procedures and local privacy related regulations
- Maintain awareness of changes to/ new regulations affecting pharmacovigilance activities. Communicate new or changed regulations to management and to relevant members of the department in order to initiate any change in process
- Coordination with different stakeholders for data request for fulfillment of pharmacovigilance responsibilities
- Support medical information activities and co-ordinate with stakeholders
- Support in activities related to pregnancy prevention program and controlled distribution of Lenalidomide. This includes but is not limited to pharmacy registrations, PAF reviews, PAF database update, follow-ups with pharmacies, reconciliations with wholesaler and pharmacies, coordination with internal stakeholders etc
Associate Medical Manager, PSS - Covance Inc. - Regionally Based, India
(2020-12 - 2022-01)
- Implement and promote use of consistent, efficient and quality process to meet timelines and deliverables according to requirements and standard operating procedures
- Ensure compliance of operations with governing regulatory requirements
- Create, maintain and assume accountability for a culture of high customer service
- Undertake primary medical review of cases, including medical assessment of the case for seriousness, Listedness/labeling, causality, adverse event coding and narrative review
- Update document daily case data, case feedback in appropriate trackers/tools to facilitate tracking and workflow management
- Assume complete responsibility for all assigned deliverables in line with expected quality, compliance and productivity SLAs and KPIs
- Undertake and complete additional tasks and activities, assigned by supervisor as required
- Provide training and guidance to the case processing team on medical aspects of case processing
Medical Officer, Department of Medicine - Employees State Insurance Scheme (ESIS) Hospital, Mumbai, India - Mumbai, India
(2019-12 - 2020-12)
- Attended patients in outdoor patient's department
- Attended ward rounds
- Attended to patients in emergency on 24 hours on-call duty
Medical Officer, ICU - Shantiniketan Nursing Home, Mumbai, India - Mumbai, India
(2019-06 - 2019-08)
- Attended to patients in ICU
- Performed procedures like cardiopulmonary resuscitation, central venous catheterization
Medical Officer- Department of Urology/CVTS - Nanavati Superspeciality Hospital, Mumbai, India - Mumbai, India
(2018-10 - 2019-01)
- Attended to Patients in Urology and Cardiovascular Thoracic Surgery Department with completion of their admission notes, carrying ward rounds, completion of pre- operative check
- Assisted senior Consultants with operative procedures in Urology and Cardiovascular surgeries
Post Graduate resident - Lokmanya Tilak Municipal Medical College and Sion Hospital, Mumbai, India - Mumbai, India
(2014-07 - 2017-07)
Post graduate curriculum – Has been working in nodal centers under pharmacovigilance India program for adverse event data collection. Opd clinical experience during pharmacovigilance training – 3 years.
- Pharmacovigilance cases feeding in Vigiflow database during post-graduation training
- Conducted and attended seminars, journal presentations as per post graduate training program
- Conducted animal experiments and assisted in maintenance of animal house with animal house in-charge
- Conducted lectures and practicals for Under-Graduate students and nursing students
- Conducted causality assessment of adverse drug reaction cases and reported to seniors for further corrections
- Uploaded pharmacovigilance cases in Vigiflow database for monitoring
- Conducted pharmacovigilance case presentations pertaining to adverse drug reactions
Medical Officer – Wards/Consulting - Shantiniketan Nursing Home, Mumbai, India - Mumbai, India
(2013-02 - 2014-06)
- Conducted ward round with senior consultants
- Perform procedures like foley's catheterization, Ryle tube insertion, dressings
- Consulted patients in the opd, catering to malaria, enteric fever, leptospirosis, dengue, Myocardial infarction, hemiplegia etc cases