**MEDICAL MANAGER** **Mexico City** **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. **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 Apply Now (https://www.jobs.abbott/) Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com