Director, Clinical Science — Global Trial Strategy

Alnylam Pharmaceuticals, Inc.; United States; On-site; USD 180,000 - 260,000; Full time

Job summary

Alnylam Pharmaceuticals seeks a Director, Clinical Science to lead scientific strategy within the global clinical development team. You will guide study design, protocol development, and clinical study execution, contributing to regulatory submissions and responses.

In this role you will chair cross-functional trials, ensure robust data review, and collaborate with medical safety, pharmacovigilance, and investigators. This position is based in the United States.

Qualifications

• College degree in life sciences or nursing; advanced degree preferred; 10+ years in pharma/biotech.
• Experience in cardiovascular and large outcome trials preferred.
• Proven track record executing multiple proof-of-concept and pivotal trials; HA interactions a plus.
• Strong scientific/analytic ability and strategic/tactical thinking.
• Ability to work in multifunctional, multinational teams and multitask.

Responsibilities

• Clinical science expert for assigned studies, maintaining current knowledge in therapeutic areas.
• Independently leads clinical execution of studies and may be accountable for program-level deliverables.
• Input to protocol design; leads development of protocol and related letters.
• Represents clinical science in protocol reviews and interacts with KOLs and Health Authorities.
• Ensures development of Study Informed Consent Documents and responses to stakeholders.

Skills

Scientific ability

Analytic skills

Strategic thinking

Multitasking

Team leadership

Education

Bachelor's degree in life sciences or nursing

Advanced degree (PhD/PharmD/MS)

Job description

Alnylam Pharmaceuticals seeks a Director, Clinical Science to lead scientific strategy within the global clinical development team. You will guide study design, protocol development, and clinical study execution, contributing to regulatory submissions and responses.

In this role you will chair cross-functional trials, ensure robust data review, and collaborate with medical safety, pharmacovigilance, and investigators. This position is based in the United States.