Bristol Myers Squibb

Sr.GlobalTrialAssociate

₹22–35L ~AI est. India FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“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.

Problems you'll solve

Risk identification; Problem resolution; Assess situation

Eligibility Requirements

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

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