Gerente Médico

Abbott; Ciudad de México; On-site; MXN 700,000 - 1,100,000; Full time

Benefits offered by this job

Career development

Global recognition

Diversity & inclusion

Job summary

Abbott in Mexico City is seeking a Specialist in Medical Affairs to oversee and execute complex clinical trials, data collection, and regulatory reporting within our Established Pharmaceutical Division.

The role requires strong knowledge of Medical Affairs, ability to manage multi-disciplinary projects, and collaboration with investigators, regulators, and external partners to ensure high-quality study outcomes.

Qualifications

• English language proficiency required.
• Experience as an MSL in the pharmaceutical industry is preferred (1–3 years).
• Relevant degree(s) as above.

Responsibilities

• Oversee direction, planning and execution of Medical Affairs activities.
• Coordinate clinical protocols and final reports.
• Recruit clinical investigators and negotiate study design/costs.
• Direct human clinical trials, Phases III & IV for products under development.
• Participate in adverse event reporting and safety monitoring.
• Prepare reports for regulatory agencies.
• Monitor study adherence and determine study completion.
• Liaise with partner organizations and licensing agreements as needed.

Skills

English language proficiency

Education

Bachelor's degree

Doctoral degree / Medicine

Job description

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

MEDICAL MANAGER

Mexico City

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to :

• Career development with an international company where you can grow the career you dream of .
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Mexico location in the Established Pharmaceutical Division. We are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory. We are looking for a specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions.

What You’ll Do

• As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization 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

• Bachelor's degree
• Doctoral degree / Medicine;
• Experience in similar role, minimum a year or 3 years of experience as a MSL in the pharmaceutical industry.
• English language proficiency

Abbott is an Equal Opportunity Employer, committed to employee diversity.