Bristol-Myers Squibb is a global Biopharma company committed to a single mission : to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference.We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development.
Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
CTM activities for Argentina and Chile including activities such us : Country feasibility, site selection, ICF revision, logistic planning for start up, site training (including SIV, Investigator Meeting organization and presentations), importation and local purchase process oversight, regulatory oversight of the study, recruitment strategies, site preparation for audit readiness, Monitoring report revision.
B.S. degree in Science. Strong scientific background, good computer skills, ability to interact and communicate, both written and oral.
Thorough understanding of ICH-GCP guidelines and local regulatory guidelines or regulations as they apply to protocol / site management.
Knowledge of general clinical research including Investigator site issues, important milestones and strategies to ensure timelines are met.
A detailed understanding of project planning and management methods. 5-7 years’ experience in clinical trial monitoring or clinical trial project management
Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.