CTM - Atopic Dermatitis (dermatology) experience required
Thermo Fisher ScientificSalary not specified
Full Time
Mid-level (3 to 4 years), Senior (5 to 8 years)
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, BiotechnologyIndustries
Requirements
- Senior leadership experience in global clinical trials and Global Development Operations (GDO)
- Expertise in strategic planning, risk management, and decision-making for complex clinical programs
- Ability to lead cross-functional study teams and manage vendor relationships
- Proficiency in study management systems (e.g., Veeva CTMS, eTMF)
- Strong collaboration skills with internal (GDO, R&D, Commercial) and external stakeholders
- Knowledge of regulatory standards, quality benchmarks, and trial feasibility assessment
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 and external contributors
- Serve as decision maker for complex issues, identify and manage risks, balancing cost, deliverables, quality, and timelines
- Manage high-value study budgets, contracts, and scope of work (SOW) for CROs and vendor partners
- Participate in vendor selection, evaluation, and strategic oversight of vendor relationships
- Set and monitor performance metrics, resolve operational challenges, and utilize quality indicators for trial execution
- Maintain accurate data records in study management systems (e.g., Veeva CTMS, eTMF)
- Establish and maintain study-level project management tools (e.g., action logs, decision trackers, issue registers, risk mitigation plans)
- Lead global initiatives, mentor future leaders, influence organizational strategy, and represent the organization in internal/external forums
- Foster innovation, process improvements, and strategic partnerships across GDO, R&D, Commercial, and other stakeholders
Skills
Key technologies and capabilities for this role
Questions & Answers
Common questions about this position
What benefits does Bristol Myers Squibb offer?
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.
Is this a remote position or does it require office work?
This information is not specified in the job description.
What are the key skills required for the Director, Global Trial Lead role?
The role requires strategic leadership, project management for complex clinical trials, risk management, cross-functional team leadership, and collaboration with internal and external stakeholders.
What is the company culture like at Bristol Myers Squibb?
The culture emphasizes challenging, meaningful, and life-changing work, growth opportunities with high-achieving teams, balance, flexibility, innovation, and continuous improvement.
What makes a strong candidate for this Director, Global Trial Lead position?
Strong candidates will have experience providing strategic leadership for global clinical trials, leading cross-functional teams and vendors, driving process improvements, and collaborating across R&D, Commercial, and other stakeholders.
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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