Bristol Myers Squibb Clinical Site Manager in Citi Center, Mexico

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.

The Clinical Site Manager is responsible for/expected to:

  • Applies project management skills to plan for the study milestones and drivers. Keeps all stakeholders informed, escalate issues with proposals and drive solutions in coordination with other departments (as applicable)

  • Manages activities at the site and monitors study progress by providing guidance as required and by close collaboration with other key stakeholders (e.g. Medical Monitor, Protocol Manager, Clinical Trial Associates, Contract Administrators, Clinical Data Quality Managers and Site Monitor(s)) as applicable. Documents substantive contacts concisely and in accordance with SOPs.

  • Disseminates information to appropriate team members to ensure timelines are met . Proactively identifies and resolves issues noted during site management which impact the overall protocol timelines and informs the appropriate BMS team members

  • In collaboration with other roles assesses whether the budget per patient is suitable to carry out the study. Participates in budget negotiations with sites, as required.

  • Demonstrates understanding of Expected Areas of Competence as stated within this position profile and demonstrates some project management Knowledge, Able to lead small teams using the PM tools. Still improving habilities to run effective meeting with large teams.

  • Developing habilities to run effective meetings and still needs to improve skills for team motivation and creating members accountability

  • Makes decisions escalating issues to appropiate member and takes action within the scope of Site Manager responsibilities

  • Demonstrates monitoring and management skills both on site and remotely.

  • Ability to exhibit more flexibility to change and being receptive to new systems and processes;

  • Applies project management skills to plan for the study milestones and drivers. Keeps all stakeholders informed, escalate issues with proposals and drive solutions in coordination with other departments (as applicable)

  • Manages activities at the site and monitors study progress by providing guidance as required and by close collaboration with other key stakeholders (e.g. Medical Monitor, Protocol Manager, Clinical Trial Associates, Contract Administrators, Clinical Data Quality Managers and Site Monitor(s)) as applicable. Documents substantive contacts concisely and in accordance with SOPs.

  • Disseminates information to appropriate team members to ensure timelines are met . Proactively identifies and resolves issues noted during site management which impact the overall protocol timelines and informs the appropriate BMS team members

  • In collaboration with other roles assesses whether the budget per patient is suitable to carry out the study. Participates in budget negotiations with sites, as required.

  • At least 4 years of experience in clinical trials (either in pharmaceutical industry or investigational sites) including some experience as project manager. Drives study level activities and deliverables in partnership with the Protocol Manager. Capable of independent decision making regarding problem solving and solution identification and implementation to meet Protocol objectives. Leads or actively participates in non-project initiatives or business workstreams.

  • Bachelors degree in a health- administrative related field and or developmental/clinical experience.

  • English language High Intermediate - advance level, both written and oral

  • Have knowledge of ICH-GCP but understand commonly- used concepts, practices, and procedures within a particular field.

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.