Regional Medical Advisor

Thornton Tomasetti; Lucknow; On-site; INR 600,000 - 1,000,000; Full time

Job summary

Abbott in Lucknow, India, is seeking an experienced medical affairs professional to guide clinical research, data collection, and regulatory reporting activities. The role involves oversight of protocols, investigator recruitment, and management of safety reporting across trials.

The position sits within Abbott's Medical & Scientific Affairs group, located at Speed Building in Lucknow, with standard work shifts and opportunities to collaborate with cross-functional teams globally.

Qualifications

• Education: Associates Degree (± 13 years).
• Experience: Minimum 1 year.

Responsibilities

• Oversee direction, planning, execution of clinical trials/research and data collection.
• Contribute to implementation of clinical protocols and final reports.
• Recruit clinical investigators and negotiates study design and costs.
• Direct human clinical trials, phases III & IV for company products under development.
• Participate in adverse event reporting and safety monitoring.
• Coordinate reporting for regulatory submissions.
• Monitor adherence to protocols and study completion.
• Coordinate investigator initiations and group studies.
• May act as consultant/liaison with other corporations under licensing agreements.

Education

Associates Degree

Job description

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 Established Pharma

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)

Abbott is about the power of health.

For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more.

Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people.

They push the boundaries to help manage and treat some of life’s greatest health challenges.

We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings.

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

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