Director, Global Trial Leader at Bristol-Myers Squibb

Warsaw, Masovian Voivodeship, Poland

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

Passionate about strategic leadership and operational excellence in global clinical trials
Experience in driving delivery across all phases and therapeutic areas
Ability to set vision for trial execution and align with business objectives, regulatory standards, and quality benchmarks
Senior leadership within Global Development Operations (GDO) or equivalent
Skills in critical decision making, risk management, and fostering innovation/continuous improvement
Experience working closely with internal/external stakeholders on process improvements and strategic planning
Capability to lead cross-functional study teams and study vendors
Experience collaborating across GDO, R&D, Commercial, and other stakeholders
Ability to lead global initiatives, mentor leaders, and represent organization in high-stakes forums
Knowledge of study management systems such as Veeva (CTMS, eTMF)

Responsibilities

Provide leadership and oversight for multiple, complex clinical trials and programs, ensuring high-quality data and regulatory compliance
Spearhead collaboration with internal study teams and vendors to meet timelines, budgets, and quality benchmarks
Provide strategic input on study feasibility and oversee operational activities of internal/external contributors
Serve as decision maker for complex issues, identify and manage risks, balancing cost, deliverables, quality, and timelines
Manage high-value study-level budgets, contracts, and scope of work (SOW) for CROs and vendor partners
Participate in vendor selection and evaluation processes
Oversee vendor and partner relationships strategically, ensuring alignment with contracts and standards
Set and monitor performance metrics, identify/resolve operational challenges, and utilize quality indicators
Maintain accurate data records in study management systems such as Veeva (CTMS, eTMF)
Establish and maintain study-level project management tools, including action logs and decision logs

Skills

Key technologies and capabilities for this role

Clinical TrialsGlobal Trial ManagementStrategic LeadershipRisk ManagementCross-Functional TeamsRegulatory StandardsProcess ImprovementStudy Vendor ManagementStrategic Planning

Questions & Answers

Common questions about this position

What is the location for this Director, Global Trial Leader position?

The role is based in Warsaw-Poland.

What are the main responsibilities of the Director, Global Trial Leader?

The role involves strategic leadership and operational excellence of global clinical trials, driving delivery across phases and therapeutic areas, providing project management oversight for complex trials, ensuring timelines, budgets, and quality, and leading cross-functional teams and vendors.

What is the salary or compensation for this position?

This information is not specified in the job description.

What is the company culture like at Bristol Myers Squibb?

The culture is challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and a focus on balance, flexibility, innovation, and continuous improvement.

What makes a strong candidate for the Director, Global Trial Leader role?

A strong candidate is a passionate senior leader with expertise in global clinical trials, capable of strategic decision-making, risk management, leading cross-functional teams, collaborating with stakeholders, and driving innovation and process improvements.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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