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 Monitor will be responsible for :
Identifies new potential Investigators, through ongoing collaborations with medical monitors (including local staff), field medical personnel, and other medical contacts.
Assess potential Investigators and their sites.
Documents the visit, and communicate findings. Provides feedback on Potential Site Assessment findings to collaborators.
Recommends sites for consideration in future studies, as needed.
Expedites the pre-study and study initiation processes including the conduct of Pre-Study Evaluation and Site
Initiation visits. Conducts initiation visits in collaboration with Clinical Site Managers, Field Medical and / or
Protocol Managers. Orients and trains site personnel regarding the protocol, study related processes and procedures and applicable regulatory requirements.
Reviews site activities and quality through on-site visits in addition to emote management capabilities.
Monitors study sites following the monitoring plan, BMS SOPs, protocol, ICH / GCP Guidelines and other local regulations as applicable.
This includes, but is not limited to : Managing multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and / or geographic territory.
Ensures safety and protection of study subjects according to the monitoring plan, SOPs, and ICH / GCP
Guidelines and local regulations. Ensures quality of data submitted from study sites and assures timely submission of data by using the available systems to follow site activities.
Supervises overall activities of site personnel over whom there is no direct authority. Motivates / influences them to meet study objectives, including enrollment and retention goals.
Resolves study site problems / issues as they occur. More complex issues may be resolved jointly with management. Initiates, recommends, documents and communicates corrective actions as needed and follows up to ensure corrective actions are implemented.
Ensures documented follow-up to all outstanding issues / corrective actions, within the scope of this position profile, in the available systems.
Appropriately documents and promptly escalates serious or persistent outstanding issues to management and project team.
Facilitates the Regulatory Compliance audit process, as needed.
Prepares and submits written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner.
Identifies opportunities to interact, builds and strengthens professional and collaborative relationships with all internal and external stakeholders (e.
g., site and institutional personnel, Thought Leaders, internal colleagues, etc.).
Uses multiple technologies to maintain open and frequent communication with all stakeholders.
Exhibits flexibility and adaptability when facing change.
Employs good fiscal management for travel expenses, etc.
Ability to perform site management activities, as required.
Performs other tasks, as assigned or requested by line manager.