Global Clinical Safety Director: Strategy & Analysis

Madrigal Pharmaceuticals; Conshohocken (Montgomery County); On-site; USD 213,000 - 260,000; Full time

Benefits offered by this job

Flexible paid time off

Medical, dental, vision and life/disability insurance

401(k) offerings with employer match

Mental health benefits via Employee Assistance Program

Job summary

Madrigal Pharmaceuticals is seeking a Director, Global Clinical Safety Scientist to lead safety assessments for clinical products. The role requires over 12 years in clinical safety within the pharmaceutical industry.

With a salary range of $213,000 – $260,000, the position includes benefits like flexible paid time off, medical plans, and equity. Ideal candidates will have strong analytical skills, a relevant Bachelor's degree, and experience with regulatory submissions.

Qualifications

• Minimum 12 years of experience in clinical safety or pharmacovigilance.
• Prior experience in designing safety and PV processes is highly desirable.
• Experience with MedDRA and WHO Drug terminology.

Responsibilities

• Serve as the lead safety scientist for assigned projects.
• Evaluate safety data from clinical studies and summarize key findings.
• Collaborate with stakeholders to develop safety content.

Skills

Strong analytical and critical thinking skills

Excellent written and verbal communication skills

Good knowledge of global safety regulations

Experience contributing to regulatory submissions and safety reports

Detailed-oriented

Education

Bachelor’s degree in a relevant scientific discipline

Advanced degree (PharmD, PhD, NP/PA, or Master's)

Tools

Safety databases (Argus preferred)

Job description

Madrigal Pharmaceuticals is seeking a Director, Global Clinical Safety Scientist to lead safety assessments for clinical products. The role requires over 12 years in clinical safety within the pharmaceutical industry.

With a salary range of $213,000 – $260,000, the position includes benefits like flexible paid time off, medical plans, and equity. Ideal candidates will have strong analytical skills, a relevant Bachelor's degree, and experience with regulatory submissions.