Project Coordinator, Pharmacovigilance - Pune

Job description · OVERVIEW: · The Project Coordinator, Pharmacovigilance (PV) Solutions will be responsible for day-to-day administrative tasks related to TransPerfect's literature monitoring projects. This role will focus on support functions for the wider Production team, ensur ...

The Project Coordinator will be responsible for day-to-day administrative tasks related to TransPerfect's literature monitoring projects. · This role will focus on support functions for the wider Production team, · ensuring all client deadlines are met.Oversee administrative elem ...

We are looking for a highly skilled and experienced Project Coordinator to join our team in the Pharma Company. · The ideal candidate will have a strong background in Pharmacovigilance and excellent project coordination skills. · ...

The Project Coordinator will be responsible for day-to-day administrative tasks related to TransPerfect's literature monitoring projects. · ...

The post holder will provide all clients with the appropriate quality of service in a safe and cost-effective manner. The individual will comply with legal requirements and document this in the Company's Health and Safety Manual. · Take ownership of assigned aspects of quality re ...

Provide all clients with appropriate quality of service in a safe and cost-effective manner. · ...

This Telecaller will be responsible for outbound calls to prospective clients managing inquiries and providing program details for clinical research courses. · ...

The Clinical Trial Manager II serves as the clinical functional lead accountable for delivering site management clinical monitoring and central monitoring of assigned studies A CTM II is expected to independently manage the clinical central monitoring team members but may serve a ...

The Functional Quality Specialist II will provide quality of service to clients in a safe and cost-effective manner. The individual will comply with legal requirements and document health and safety procedures. · Take ownership of assigned aspects of quality reviews on projects. ...

+Job Summary · Lead the preparation and review of aggregate safety reports. Be responsible for end-to-end report management including planning, authoring and managing review approval and submission steps per project scope and requirements. · +ResponsibilitiesWrite and review vari ...

This job involves assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process. · The role requires managing and processing expeditable adverse events to the required standard, submitting them to the client and ...

The Clinical Trial Manager II serves as the clinical functional lead accountable for site management oversight. The position provides leadership problem-solving mentoring technical support ensuring compliance with monitoring plan timeliness quality within budget. · ...

The Compliance Manager will be responsible for developing implementing and managing the company's regulatory compliance strategy for Over The Counter pharmaceutical products across all domestic and international markets including e-commerce platforms This role is critical in ensu ...