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Medical Science Consultant

hace 1 semana

Buenos Aires, Buenos Aires C.F., Argentina Coca-Cola HBC A tiempo completo
Job Description
As a Medical Science Consultant at IQVIA, you will be responsible for providing medical, clinical, and scientific advisory expertise to all divisions as requested. This will involve participating in all aspects of Medical Science involvement on assigned trials, serving as a medical expert during the project delivery life-cycle. Your primary responsibility will be to provide therapeutic medical and strategic expertise to business development activities.

Key Responsibilities:
* Conduct medical reviews of protocols, Investigative Drug Brochures (IDBs), and Case Report Forms (CRFs).
* Provide therapeutic area/indication training for project clinical teams.
* Attend and present at Investigator Meetings.
* Perform review and clarification of trial-related Adverse Events (AEs).
* May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
* May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of the Pharmacovigilance department.
* May perform medical review of adverse event coding.
* Review the Clinical Study Report (CSR) and patient narratives.
* Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
* Available 24 hours a day, 7 days a week to respond to urgent protocol-related issues at the investigative sites.

Requirements:
* Excellent communication, presentation, and interpersonal skills, including command of the English language (both written and spoken).
* Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
* Certification as a Psychiatrist (mandatory).
* 3 - 5 years of prior relevant experience in general clinical medicine.
* Previous clinical research experience as an investigator or in the Pharma, CRO, or Biotech industry is required; or equivalent combination of education, training, and experience.
* Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.
* Strong Business Acumen.
* Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
* Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.