Bristol Myers Squibb

TrialManager,LateDevelopment

$12000–18000k ~AI est. Otemachi, Japan FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Trial Manager, Late Development at Bristol Myers Squibb. Skills: Project management, Clinical trials, Stakeholder management. Manage protocols for operational execution. Support management of issues”

Industry & Context.

Problems you'll solve

Risk identification; Risk neutralization

What They're Looking For.

Must Have

2-4 years project management experience, 1 year pharmaceutical or healthcare experience, GCP, ICH Guidelines knowledge, Clinical research processes knowledge, Microsoft Suite proficiency, Clinical Trial Management Systems experience

Nice to Have

Japanese language proficiency

What You'll Do.

Manage protocols for operational execution

Support management of issues

Support management of risks

Support management of timelines

Support management of budget

Foster partnerships across multidisciplinary teams

Monitor trial progress

Lead study team meetings

Address and manage obstacles

Escalate appropriately

Manage quality systems

Comply with quality systems

Manage compliance systems

Lead operational start-up

Lead operational maintenance

Lead operational close-out

Serve as primary point of contact

Liaise with Medical stakeholders

Liaise with global stakeholders

Monitor study progress

Ensure data deliverables are met

How You'll Work.

Team & Collaboration

Multidisciplinary teams; Cross-functional teams

Communication Scope

Verbal communication; Written communication

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). **Position Summary** Responsible for operational execution of Late Development Book of Work across various therapeutic areas and study types (e.g., NIR, ISR, PAA, Phase IV). Act as point of contact for external study sponsors and internal stakeholders. **Duties/Responsibilities** * Manages protocols within a complex matrix environment for successful and timely operational execution of research from start to end * Focused on project management concepts to support management of issues, risks, timelines, and budget * Leverages interpersonal and influencing skills to foster partnerships across multidisciplinary teams _BMS-Sponsored Studies_ * Monitor trial progress and study budget * Lead study team meetings * Address and manage obstacles * Identify issues and risks, escalating appropriately * Oversee vendors * Manage and comply with various quality and compliance systems _Non-BMS Sponsored Studies_ * Lead operational start-up, maintenance, and close-out * Serve as primary point of contact for study Sponsor * Liaise with Medica

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