Regional Medical Advisor

Abbott India Ltd; Lucknow; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Abbott India Ltd seeks a Regional Medical Advisor to supervise the direction, planning, and execution of clinical trials and data collection in India. The role requires handling protocols, reports, and safety responsibilities, with recruitment and negotiation of study designs with investigators.

The candidate should have an Associates Degree and at least 1 year of relevant experience in Medical Affairs or clinical research, with the ability to coordinate trials across multiple sites in Lucknow

Qualifications

• Associates Degree required.
• Minimum 1 year of experience in Medical Affairs or related field.
• Experience with clinical trials, data collection, and safety reporting was noted.

Responsibilities

• Oversee direction, planning, execution of clinical trials and data collection activities.
• Contribute to implementation of clinical protocols and final reports.
• Recruit clinical investigators and negotiate study design and costs.
• Direct human clinical trials (Phases III & IV) for products under development.
• Participate in adverse event reporting and safety responsibilities.

Skills

Clinical research

Trial coordination

Data collection

Education

Associates Degree

Job description

Regional Medical Advisor JOB DESCRIPTION:

MAIN PURPOSE OF ROLE

Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements.

MAIN RESPONSIBILITIES

• As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills 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 Education Level : Associates Degree (± 13 years)

Experience/Background Experience : Minimum 1 year

The base pay for this position is N/A In specific locations, the pay range may vary from the range posted.

JOB FAMILY: Medical & Scientific Affairs

DIVISION: EPD

LOCATION: India > Lucknow : Speed Building

ADDITIONAL LOCATIONS:

WORK SHIFT: Standard

TRAVEL: Not specified

MEDICAL SURVEILLANCE: Not Applicable

SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Experience Level Senior Level