Snehal Parmar, Ms Email & Phone Number

Edmonton, Ab, Ca

Canada

• Servers as project manager for large scale Project by working with functional teams to ensure timely and high-quality deliverables• Oversees case processing, medical review, regulatory reporting, literature review, aggregate reporting, PSMF oversight, and medical information activities.• Present weekly and monthly quality and compliance data with analysis of root causes and potential CAPA.• Reviews and implement project plans and PV agreements with business partners and MAHs.• Actively participates in customer and agency audits and inspections and assists in audit activities, risk management plan, risk identification and risk mitigation strategies implementation with QA, Operations, and senior leadership teams.• Provides leadership of global project teams of more than 100+ staff• Develops program specific documents (i.e., transition plans, safety management plan, quality management plan, communication plan, etc.)• Accountable as primary point of contact for IQVIA customers, including leading project team meetings• Ensures quality and timely deliverables for assigned projects, while providing continuity during project startup, maintenance, and close out• Collaborates with customer to establish mutually agreed working practices, standardizing procedures across the program

Mississauga, Ontario, Canada

• Accountable for ensuring appropriate process is in place for receiving, collecting, processing and submitting PV data to clients. • Managed timely processing of safety data by overseeing departmental workload, prioritizing critical cases, and managing a team of 10 associates. • Authored and maintained PV training materials and delivers Pharmacovigilance training for employees and contractors to adhere to PV requirements. • Facilitated and coordinated in external and internal audit and conducts self-inspections. • Wrote and implemented Work instructions and Standard Operating Procedures. • Provided inputs to licensing agreements and third-party contracts for safety data reporting processes

Mississauga, Ontario, Canada

• Reviewed and processed over 9000 adverse event reports for the department and submitted to clients within the set timeframe.• Promoted to position of specialist Pharmacovigilance in about a year for exceptional performance which helped improve the overall departmental compliance. • Collaborated with the clinical, nursing, reimbursement and customer service teams to ensure the pharmacovigilance activities are performed in timely manner. • Initiated over 350 deviations and documented root cause analysis and CAPA. • Trained 04 PV associates on PV database and internal and external processes.• Participated successful audits, helped in audit readiness in maintaining the trackers and document files. • Trained over 100 employees on drug safety requirements to maintain pharmacovigilance awareness. • Performed monthly reconciliations and Quality Control checks.• Provided inputs to the project management and business development teams on Pharmacovigilance processes.• Shared regular reporting on project metrics to the senior manager and director.

Mississauga, Ontario, Canada

• Took ownership of individual products assigned and comply with specific reporting requirements.• Received, reviewed and documented all pertinent clinical information in compliance with SOP/protocol and applicable legislation.• Data entry into program-specific databases. • Participated in team discussion for both processing and product knowledge.

Mumbai Area, India

• Collected, reviewed and processed over 4000 adverse event reports from spontaneous, literature and Solicited sources in the safety database (SEPTRE).• Generated regulatory reports, including CIOMS, E2B files, line listings and Aggregate reports as per the local regulatory requirements. • Met the Health Authority deadlines with 100 % compliance (First half of 2017) which resulted in recognition with "Encore Gold Award”. • Acted as the primary receiver for all AE reporting by monitoring the safety mail boxes. • Successfully monitored and reported adverse events by liaising with cross-functional teams.• Made sure the pharmacovigilance agreements (PVA) is implemented by vendors and international business partners. • Placed queries, conducted follow-ups and closed answered queries as requested by global teams and health authorities. • Conducted new employee training and annual refresher training for entire field force.• Generated the product quality complaints investigation and tracking the ETS/PQMS numbers.

Mumbai Area, India

• Reviewed source documents including lab results, discharge summaries and other medical documents to find and report adverse events.• Processed over 6000 the safety reports in database (ARGUS), assessed regulatory status which is seriousness and expectedness/relatedness to prioritize workload.• Wrote case narratives and coded medical history, concomitant medication, adverse events (using MedDRA and WHODD).• Prioritized workload and liaise with other safety associates to meet reporting deadlines.

Maroli- India

• Dispensed medication as a pharmacist in a busy community pharmacy with around 100 to 150 prescriptions a day. • Worked toward improving peoples' health by providing advice and information.• Managed the pharmacy medication orders, supply with in the hospital and stocks with expiry medication management.

London, United Kingdom

• Interact with clients, vendors and visitors.• Answer telephones and transfer to an appropriate staff member. • Perform general clerical duties to include, but not limited to, bookkeeping, photocopying, faxing, filing and emailing.• File and retrieve organizational documents, records and reports.• Attend Board, committee meetings or other meetings as requested in order to record minutes.• Support staff in assigned project‐based work, Work flexibly and as a part of the team to help colleagues as necessary. • Deal with the enrolment of the new learners and their induction to the new course.

London, United Kingdom

• Provided front line customer care services which involved dealing with customers of different cultures, helped me develop my people's skills.• Selected to deputise for the store manager, gained good resource management and people management skills. • Responsible for ordering stock from the suppliers and dealing with telephone inquiries as well as web orders.• Managing the till, taking money from customers and hanging out receipts.• Following policies and procedures relating to cash & stock handling.• Checking the inventory listing with the actual stock on the shop shelves and reporting any discrepancies to managers.

Surat Area, India

• Worked on providing an interface between pharmaceutical companies and healthcare professionals.• Successfully structured and organized healthcare programs at local medical practices and hospitals, working on building greater awareness for diabetes.• Focusing on organizing medical conferences to aid, identify and introduce optimal products and solutions within the pharmaceutical sector.• Continuously building a positive working relationship with medical professionals, whilst providing consistent support with administration staff.

M.Sc, Pharmaceutical Science

Activities and Societies: Research Assistant internship for three months with the University. Publication: Metabolomics of four TCM herbal.

Bachelor Of Pharmacy - Bpharm, Pharmacy

Activities and Societies: Inter college competition (singing, extempore speech) Player of College Cricket and Volleyball teamA four year.