Endocrinology Clinical Development Lead

Vertex Inc.; Boston (MA); Hybrid; USD 240,000 - 360,000; Full time

Benefits offered by this job

Medical, dental and vision benefits

Paid time off including company-wide休?

Educational assistance programs

Student loan repayment

Commuting subsidy

401(k)

Job summary

Vertex is seeking a Clinical Development Medical Director to serve as Medical Lead for multiple clinical trials across all phases. You will work with cross-functional teams on trial strategy, design, and execution, and monitor safety as the Medical Monitor.

The role requires medical leadership, extensive experience in clinical development, and strong communication and regulatory submission skills. Hybrid-eligible or on-site in Boston area, with comprehensive Total Rewards.

Qualifications

• MD, DO or equivalent ex-US medical degree
• Board certification/eligibility in a specialty field is highly desired
• Typically requires 10 years of basic or clinical research experience
• Experience in analysis of research data and publications; knowledge of biostatistics; knowledge of GCP and clinical study design
• Experience with design, execution, and analysis of clinical trials

Responsibilities

• Leads the development of study protocols and other key study documents
• Serves on cross-functional Study Execution Teams for assigned trials
• Participates in regulatory submissions and safety reports for regulatory authorities
• Provides scientific input to study documents and analysis plans; liaises with Regulatory Affairs and Clinical Operations
• Represents Vertex to outside medical personnel in protocol development and study conduct
• Performs other duties related to clinical programs

Skills

Excellent communication

Cross-functional collaboration

Medical leadership

Endocrinology knowledge

Education

MD/DO or equivalent

Board certification/eligibility in a specialty

Job description

Vertex is seeking a Clinical Development Medical Director to serve as Medical Lead for multiple clinical trials across all phases. You will work with cross-functional teams on trial strategy, design, and execution, and monitor safety as the Medical Monitor.

The role requires medical leadership, extensive experience in clinical development, and strong communication and regulatory submission skills. Hybrid-eligible or on-site in Boston area, with comprehensive Total Rewards.