Global VP, Clinical Development & Strategy

Visa Hunt; United States; On-site; USD 345,000 - 375,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Paid time off

Professional development

Job summary

Codera, a Tang Capital company, seeks a Vice President of Clinical Development to steer regulatory strategy and execution for domestic and international programs. You will oversee biometrics, medical writing, safety monitoring and pharmacovigilance across asset portfolios, reporting to the Chief Development Officer, with broad global oversight.

You will guide trials from early to late phases, ensure regulatory submissions are rigorous, and lead teams to deliver high-quality data and analyses.

Qualifications

• 10+ years of clinical development experience in biotech/pharma.
• Experience leading teams through early-to-late development and regulatory submission.
• Deep knowledge of global regulatory requirements and trial-to-approval processes.

Responsibilities

• Oversee clinical development programs including strategic planning and execution of clinical trials.
• Evaluate and refine development strategies to mitigate risks and expedite assets.
• Direct planning, delivery and leadership of clinical trials from early to late phases.
• Lead development of trial protocols with scientific rigor and regulatory compliance.
• Assume medical and clinical accountability, including safety monitoring and risk management.
• Oversee biometrics and medical writing to summarize studies per timelines and quality standards.
• Collaborate with Regulatory Affairs to enable trial approvals and submissions.
• Direct data analysis and reporting to support decision-making and submissions.

Skills

Leadership

Strategic thinking

Regulatory knowledge

Cross-functional collaboration

Communication

Education

Bachelor's Degree

Advanced degree preferred

Job description

Codera, a Tang Capital company, seeks a Vice President of Clinical Development to steer regulatory strategy and execution for domestic and international programs. You will oversee biometrics, medical writing, safety monitoring and pharmacovigilance across asset portfolios, reporting to the Chief Development Officer, with broad global oversight.

You will guide trials from early to late phases, ensure regulatory submissions are rigorous, and lead teams to deliver high-quality data and analyses.