Average salary: Rs237,500 /yearly
More statsSearch Results: 166,686 vacancies
...alone projects and programs, and the main pharmacovigilance point of contact for assigned full-... ...recommends improvement plans to projects.
• Manages resources and resource projections to... ...staff.
• Performs metric collection and data analysis to support company efforts for...
...research solutions, quality compliance, pharmacovigilance, medical information, and RD technology,... ...checking the completeness and accuracy of the data entered in the various fields.... ...Request follow-up and perform query management, as applicable.
Maintaining respective...
...Job Description
Skill required: Pharmacovigilance Operations - Safety Writing
Designation... ...unique insights into the patient experience.
Management of the Affiliate Mailbox, reconciliation... ...SOP.
• Narratives are written based on data listings and/or safety reports (e.g.,...
...Role & responsibilities
Conduct and execute all pharmacovigilance related activities in Unichem lab.
Train PV Team, corporate office... ...) and submitting it to the regulatory authorities and risk management plans (RMPs) contribute to pharmacovigilance matrix to ensure...
...obligations.
• Serve as support to the Safety Reporting Group management in all aspects of departmental activities, including but not... ...multiple databases. Maintenance of project information or Pharmacovigilance intelligence information with timely updates to the project or...
Remote job
...safety review of clinical and diagnostic data for case processing
• Assist with... ...and efficient development of the Safety Management Plan, including development of specific... ...projects as assigned; coordinates teams of Pharmacovigilance associates on project level and serves as...
Remote job
...Scientific Unit and other relevant groups within and outside of Teva Pharmacovigilance.
Quality control of literature reviews performed within... ...including literature review process in ICSR/Signal Management/PSUR.
Reports To
~ Sr. Mgr Pharmacovigilance
Teva's...
...The Senior Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs...
...Core member of the safety team and is responsible for performing pharmacovigilance activities within the North American PV unit, in partnership... .../Pharmacovigilance Safety Specialist and Pharmacovigilance Managers/Director to receive and review adverse event information for pre...
...Job Summary
We are looking for Associate Pharmacovigilance to join our Pharmacovigilance (PV) team (offices working in Hybrid model). This is an amazing opportunity to support the team to perform literature monitoring and assessing for adverse events reporting, indexing...
...the Single Point of Contact (SPOC) for the contracted Pharmacovigilance activities and assists Project Manager for project operation oversight.
• Provide... ...and compliance for safety deliverables and provides data metrics for inclusion in monthly project reports. Additionally...
...Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company representatives
Assess the severity and causality of adverse...
...Pharmacovigilance Associate Responsibilities:
Process and manage adverse event reports: This includes reviewing AE reports from healthcare professionals, patients,... ...Pharmacovigilance Associates enter and maintain AE data in safety databases. This data is used to track trends...
...actions (e.g., requirements updates) as designated
Reviews Safety Management Plans with regard to documented country-specific regulatory... ...project tracker) as designated; ensures completeness, accuracy and data integrity; suggests enhancements to gain efficiencies...
~ The Pharmacovigilance (PV) Associate I will support administrative and operational activities for Signal Detection (SD), Safety Data Review (SDR) and Scheduled Aggregate Reports (SARs), Safety Management Team (SMT) system set-up, access support, data coordination, and tracking...
...part of a project team, performing, and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance
PV Officers are... ...workflow cycle, except Medical Review.
Independent SAE/SUSAR Management (submissions, unblinding, clinical trial reconciliations)...
...achieved by:
· Assume responsibility for management of client and client products.
· Serve as a resource for pharmacovigilance team on the procedures and processes for adverse... ...other stakeholders for the purpose of safety data collection, data reconciliation, etc.
·...
~ The Executive Pharmacovigilance will be responsible end-to-end case management, including case receipt, facilitation of case follow-up, case download from regulatory... ...and safety files.
Prepare and share compliance data with QPPV.
Provide data for compliance representation...
...narratives of cases and checking the completeness and accuracy of the data entered in the various fields.
Performs clear and accurate... ...accurate for the events.
Request follow-up and perform query management, as applicable.
Maintaining respective trackers required for...
...position is a member of Global Patient Safety – Pharmacovigilance Compliance and Safety Operations -PV... ...Support team. This position is responsible for managing systems and databases to support consistent and accurate pharmacovigilance data collection, data analysis, report...
