At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Co-op, Clinical Data Management is a supporting role to the Clinical Data Management function within GDMCM providing a learning opportunity for the co-ops to understand Clinical Data Management activities and its importance in the execution of clinical trials. The position will report into Associate Director, Clinical Data Management and work closely with a Data Management Lead.

This is an office-based position located in San Diego, CA.  The resource will have the option of working remotely 50% of the time per company policy.  Office requirements are subject to change based on company and local government guidelines during the COVID-19 pandemic.  COVID-19 vaccination documentation is required to be submitted to be on-site.  BMS offices have mask and other public health guidelines in place.  Weekly COVID-19 testing is required and is available on-site at no cost to employees.

Key Responsibilities

• Completion of assigned GCP and Clinical Data Management trainings
• Read and understand the clinical trial protocol to understand the study design and evaluate the data collection requirements
• Assist the Data Management Lead in creation of the specifications for the Electronic Case Report form
• Assist in implementation, and evaluation of data validation processes (e.g., edit checks).
• Assist in Data Review processes such as Data Quality Management Plan, Protocol Data Review Plan, External Data Reconciliation and SAE reconciliation Plan.
• Learn about different vendors providing data for clinical trial and assist with vendor data quality oversight
• Participate and assist in the Database Lock planning and execution
• Learn about eTMF and its importance in clinical trials and good documentation practices

Qualifications & Experience

• Aspiring to completion of Bachelor’s Degree in life sciences/healthcare/data science/Project Management
• Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
• Strong oral and written communication skills
• Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications.
• Strong knowledge of Microsoft Office skills
• Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors
• Basic knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management
• Ability to learn quickly

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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 with the resources to pursue their goals, both at work and in their personal lives.

Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, hematology, immunology, cardiovascular, fibrosis and neuroscience. Our employees work every day to transform patients’ lives through science.