pharmacovigilance scientist Openings in Hyderabad – PV

Pharmacovigilance Scientist, ICSR (India) vacancies in Hyderabad for Freshers & Experience Candidates

Job Description

• The PV Scientist will be responsible for processing of ICSRs (Individual Case Safety Reports) with a great working knowledge of the adverse event safety profile of the assigned drugs, labelling documents, client’s guidelines, SOPs, and Global drug safety regulations.

Essential Functions Include:

• Monitoring of incoming reports from various sources viz mailboxes, EudraVigilance and literature searches etc.
• Downloading of L2A (Regulatory authority) and MLM cases from EV Web on regular basis by using client specific filters for triage process.
• Triage of incoming reports for completeness, duplicate check, legibility, and validity.
• Perform literature searches according to search strategy.
• Responsible for sending translation requests.
• Responsible for data entry of individual case safety reports into the safety database
• Full data entry including medical coding and safety narrative

As Medical Coder:

• Responsible for coding all medical history, events, drugs /procedures/indication and laboratory tests according to the appropriate dictionary (For e.g., MedDRA, Company Product Dictionary, WHO-DD)

As Narrative Writer:

• Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
• Performs clear and accurate data capture of cases in accordance with client conventions/guidelines and Standard Operating Procedures (SOPs).
• Ensures that the expectedness, causality assessment as well as seriousness criteria are accurate for the events.
• Request follow-up and perform query management, as applicable.
• Maintaining of respective trackers required for the process and client delivery.
• Maintaining an awareness of global regulatory reporting obligations and organizing work to ensure compliance with internal and regulatory timelines for the adverse event reporting
• Attend internal, drug safety and project-specific training sessions
• Finishes training assigned on internal and client Learning Management System (LMS) as applicable
• Liaising as well as collaborating with the relevant function at the client’s end to help with the delivery of high-quality work.

Qualifications

Qualified candidates must have:

PhD, BDS, M-Pharmacy / B-Pharmacy, Doctor of Pharmacy (PharmD) from PCI recognized University/College.

Experience:

• Fresher 0-2 years of experience in case processing.
• Excellent verbal, written and interpersonal communication skills.
• Strong organization and prioritization skills; able to multitask.
• Computer proficiency, IT skills, the expertise, and an ability to deal with web-based applications, and familiarity with the Windows Operating system and the MS Office suite (Word/Excel/PowerPoint).
• Capability to evaluate data and draw conclusions independently.
• Understanding of patient safety regulatory obligations
• Flexibility to adapt and meet fluctuating business priorities.
• Able to occasionally work extended and/or flexible schedule to meet client requirements.
• Capability to work collaboratively as well as efficiently in a team environment.
• Client focused approach to work

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting

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