Bristol Myers Squibb
Sr.GlobalTrialAssociate
Neural analysis suggests this role is
optimal for Senior candidates.
“Sr. Global Trial Associate at Bristol Myers Squibb. Skills: Global Trial Management, Clinical Research Operations, Study Documentation, Cross-functional Collaboration. Manage study documentation development. Support Global Trial Lead”
Industry & Context.
Risk identification; Problem resolution; Assess situation
Travel less than 5%
What They're Looking For.
Must Have
2-4 years experience in Clinical Research, Global experience preferred
Nice to Have
BAS in relevant discipline, Knowledge of clinical research budgets, Working knowledge of project management
What You'll Do.
Manage study documentation development
Support Global Trial Lead
Provide operational input
Facilitate operational processes
Use performance metrics
Use quality indicators
Identify risks proactively
Implement action plans
Resolve routine problems
Escalate important issues
Contribute to cross-functional teams
Provide input to study tools
Provide input to study plans
Perform core GTA tasks
Escalate appropriately
Push back appropriately
Delegate appropriately
Contribute to study meetings
Lead assigned components
Assist Global Trial Lead
Contribute to oversight
Oversee country regulatory approvals
Oversee country site approvals
Oversee IRB/IEC approvals
Oversee IRB/IEC notifications
Work on various trials
Contribute to initiatives
Identify path forward
Understand task interdependence
Participate in study meetings
Capture meeting minutes
Support study CSR appendices
Manage vendor payments
Track vendor payments
Lead study closure activities
Lead study archival activities
How You'll Work.
Team & Collaboration
Cross-functional global teams; Key stakeholders; Internal stakeholders; External stakeholders
Communication Scope
Oral communication; Written communication; Presentation skills
Process & Methodology
Project management
Full Job Description
**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 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. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). **Duties/Responsibilities** **Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to the following:** **_Project Management_** * Manages the development and/or collection of study level documentation & support Global Trial Lead (GTL) in ensuring eTMF accuracy & completion of for all studies * Provides operational input and facilitates operational processes as an SME in support of the startup, maintenance, and closure of studies. * Uses performance metrics and quality indicators to assist the Global Trial Lead (GTL) in driving study execution. * Proactively Identifies risks and develops/implements action to avoid or mitigate. * Resolves routine problems and escalates important issues appropriately (with a sense of urgency). * Actively contributes as a key functional member on cross-functional teams. **_Study/Project Planning, Conduct and Management_** * Provides and support input to study level tools and plans while wo
Applying for this Sr. Global Trial Associate role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Bristol Myers Squibb?
Real rants from real employees. Read before you apply.