Global Clinical Science Manager, Cardiovascular Partnerships

Bristol Myers Squibb; England; Hybrid; GBP 90,000 - 130,000; Full time

Job summary

Bristol Myers Squibb seeks a Senior Manager in Global Clinical Science (Cardiovascular) to support diligence, asset valuation and clinical development planning in the UK. You will partner with senior BD leaders and cross-functional teams to shape trial design and risk assessment, contributing to governance discussions and deal strategy.

The role requires strong GCP/ICH knowledge, experience in study design, statistics and medical writing, and a track record of delivering timely, data-driven

Qualifications

• Degree in Life Sciences or related field required; industry experience preferred.
• Strong understanding of GCP/ICH and drug development timelines.
• Experience in clinical study design, statistics and medical writing.
• Ability to translate clinical data into diligence memos and deal narratives.

Responsibilities

• Collaborate with external partners and senior BD leads on diligence discussions.
• Contribute to clinical development plans from early to late development stages.
• Lead review of trial design elements to inform feasibility and valuation assumptions.
• Support asset valuation and deal feasibility through data review and trend analysis.
• Provide guidance to junior team members and collaborate cross-functionally with Biostatistics, Regulatory, and Medical Affairs.

Skills

GCP/ICH knowledge

Drug development process

Study design

Statistics

Clinical operations

Data review

Trend identification

Medical writing

Planning / project management

Deal narratives

Valuation frameworks

Education

Life sciences degree

MBA or business/finance coursework

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Data review tools

Job description

Bristol Myers Squibb seeks a Senior Manager in Global Clinical Science (Cardiovascular) to support diligence, asset valuation and clinical development planning in the UK. You will partner with senior BD leaders and cross-functional teams to shape trial design and risk assessment, contributing to governance discussions and deal strategy.

The role requires strong GCP/ICH knowledge, experience in study design, statistics and medical writing, and a track record of delivering timely, data-driven