Regulatory Affairs Lead, Biotech — Equity Eligible

Kymera Therapeutics; Boston (MA); On-site; USD 145,000 - 215,000; Full time

Job summary

Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs in Boston to lead regulatory activities for multiple drug development programs. This dynamic role involves managing regulatory submissions and providing guidance on cross-functional teams.

The ideal candidate has 5–7 years of experience in regulatory affairs, strong knowledge of US regulatory requirements, and excellent communication and problem-solving skills. A competitive compensation package includes a base salary range of $145,000 – $215,000.

Qualifications

• 5–7 years of drug development experience in regulatory affairs.
• Experience managing regulatory submissions (INDs/CTAs).
• Ability to work in a fast-paced environment.

Responsibilities

• Lead regulatory activities for drug development programs.
• Compile and author regulatory submission packages.
• Provide regulatory guidance to cross-functional teams.
• Contribute to health authority interactions.

Skills

Drug development experience

Regulatory submissions management

Knowledge of US regulatory requirements

Excellent communication skills

Problem-solving skills

Education

Bachelor’s degree in a scientific discipline

Job description

Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs in Boston to lead regulatory activities for multiple drug development programs. This dynamic role involves managing regulatory submissions and providing guidance on cross-functional teams.

The ideal candidate has 5–7 years of experience in regulatory affairs, strong knowledge of US regulatory requirements, and excellent communication and problem-solving skills. A competitive compensation package includes a base salary range of $145,000 – $215,000.