Senior Manager Medical Affairs

Abbott; Maharashtra; Presencial; INR 1.800.000 - 3.200.000; Jornada completa

Descripción de la vacante

Abbott is seeking a Senior Supervisor to lead a Medical Affairs team of more than two professionals in India. The role focuses on mentoring, coordinating, and delivering high-quality clinical trial oversight and data collection across protocols.

You will recruit investigators, negotiate study designs and costs, direct Phases III & IV trials, monitor safety and AE reporting, and ensure regulatory reporting timelines are met.

Formación

• Education requirement: Associates Degree (± 13 years).
• Minimum 4 years of experience.

Responsabilidades

• Supervises professionals in directing clinical trials, data collection, and research activities.
• Contributes to clinical protocol implementation and final report completion.
• Recruits clinical investigators and negotiates study design and costs.
• Directs human clinical trials for product development (Phases III & IV).
• Participates in adverse event reporting and safety monitoring.
• Coordinates reporting for regulatory submissions.
• Monitors protocol adherence and determines study completion.
• Oversees investigator initiations and group studies.
• May liaise with other corporations under licensing agreements.

Educación

Associates Degree

Descripción del empleo

MAIN PURPOSE OF THE ROLE

Leads/supervises a team of more than 2 professionals within the Medical Affairs Sub-Function.

MAIN PURPOSE OF THE ROLE

Leads/supervises a team of more than 2 professionals within the Medical Affairs Sub-Function.

First level manager of a work team that may comprise professionals, technical and/or administrative staff.

Typically without budget or hire/fire authority.

Focuses on mentoring, coaching, and coordination.

Main Responsibilities

• As the Supervisor of the Medical Affairs Sub-Function, supervises professionals in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• Monitors adherence to protocols and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.May act as consultant/liaison with other corporations when working under licensing agreements.

Qualifications

Education Level Major/Field of Study or Equivalent

Associates Degree (± 13 years)

Experience/Background

Minimum 4 years