Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease.
Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-
on community support. 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.
Experiences Desired :
Experience as a Senior Clinical Site Manager and Manager of Clinical Site Managers Clinical Trial Associates or equivalent in the pharmaceutical industry.
Experience in the planning, conduct, management and oversight of studies in a clinical program from study start-up to regulatory submission.
Demonstrated ability to drive project related activities.
Previous resource allocation experience.
Previous management, supervisory, and / or leadership experience (i.e., participation in task force, initiative, or cross functional team);
experience mentoring and providing feedback to others.
Experience working in a complex matrix environment.
Experience working on, or supervising, complex projects in Oncology area, particularly valued experience in working with Immunooncology protocols
Experience working with CROs as a liaison, Specialist or similar, both for outsourced projects as well as with CRO Services.
Experience working with, or supervising, all phases and types of protocols within R&D space, from Phase I to IV, and Investigator Sponsored Research (ISRs), across Latin America
Experience working within a Functional Service Providers environment
Knowledge equivalent to that attained with a Bachelor's degree and a minimum of 10 years pharmaceutical industry / R&D related experience.
An in depth knowledge of Good Clinical Practices (GCPs), International Conference on Harmonization (ICH) Guidelines, and local regulations across Argentina, Chile, Colombia and Peru.
An in-depth knowledge of clinical research including its processes, procedures, and timelines. An in-depth knowledge of the pharmaceutical industry and of the pre-
clinical, clinical, and regulatory components.
An in-depth understanding of overall planning and management of a project.
An in-depth understanding of planning and oversight of complex oncology protocols within the Immunooncology space.