Responsibilities: Prepare payroll tax deposits and other payroll reports. Issue form 941,940, 943 and W2s. Process live or after-the-fact payroll for clients Use knowledge of payroll tax filing & reporting Collect & verify time sheets Annual bonus Health insurance
Company: An MNC Pharma Company Position: Manager / Senior Manager–Product Safety Risk Management (PSRM) Experience: 10 Years Education : MBBS (MD Preferrable) Location: Hyderabad CTC: Rs. 30-40 LPA Purpose of this role: To assist in the global pharmacovigilance activities within PSRM in accordance with Company, international standards and regulatory requirements, as assigned. Key Accountabilities: Responsible for coordinating Periodic Safety Update Reports (PSUR) and Addendum to Clinical Overview (ACO) related activities (including but not limited to PSUR writing & medical review, handling of requests received from Central & Local Regulatory Affairs and PV departments) within respect of timelines and any other related task. Responsible for coordinating Risk Management Plans (RMP) related activities (including but not limited to collection of data, RMP writing and medical review, handling requests received from central or local regulatory affairs and PV department) within timely manner. Responsible for Signal Management related activity (including signal detection by company methodology, medical review of signaling reports, communication and escalation to CPSC). Responsible for assisting in: A. CCDS development, review and updating B. Maintenance of RSI. Health Authority Responses Assists in preparing or prepares responses to Regulatory Authority questions related to safety issues and conducts medical review. Provides safety input into Medical Risk Assessments (MRAs), drives the process from SST and develops and follows-up the quality issues having safety implications. Reviews and provides medical/safety inputs in the Product Information and labelling issues. Liaises with internal and external stakeholders in performance of the above-mentioned tasks. Assists in any other Pharmacovigilance department projects, as necessary. Provides medical safety expertise and training to other personnel, as necessary. Keeps current with professional and pharmacovigilance regulations and knowledge. Provides medical guidance to PV Officers/ Senior PV Officers in medical aspects of drug safety and any other personnel. Writing & update of Standard Operating Procedures (SOP). Assists or oversees any other project where PSRM (P roduct Safety and Risk Management) SST ( System Suitability Testing) is involved, as deemed necessary. Training Required: Ability to manage own workload and interact well in a team environment . Minimum 10 Years of pharmaceutical industry experience, preferably working within pharmacovigilance. Knowledge of Pharmacovigilance guidance’s Excellent time management skills and must be able to work to work seamlessly on tight timelines.