Director of Quality — GCP/GLP Oversight (Phase 3)

Braveheart Bio; Oregon (WI); On-site; USD 195,000 - 230,000; Full time

Job summary

Braveheart Bio, located in Wisconsin, is seeking a Director of Quality to oversee clinical quality and ensure compliance in its late-stage clinical programs. This critical role includes managing GCP oversight, implementing quality strategies, and developing oversight plans while collaborating closely with various teams.

The ideal candidate will possess extensive GxP experience, strong communication skills, and the ability to thrive in a dynamic environment. A competitive salary range of $195,000 - $230,000 is offered for this pivotal position.

Qualifications

• 10+ years of GxP quality experience in clinical development.
• Ability to assess risk and solve complex problems.
• Experience in rare disease or specialty disease clinical development.

Responsibilities

• Lead clinical quality strategy aligned with regulatory requirements.
• Develop and execute clinical quality oversight plans.
• Ensure inspection readiness across clinical activities.

Skills

GxP quality experience

GCP oversight

Clinical data integrity

Risk assessment

Regulatory compliance

Strong communication skills

Education

Bachelor’s degree in life sciences, health sciences or related discipline

Advanced degree preferred

Job description

Braveheart Bio, located in Wisconsin, is seeking a Director of Quality to oversee clinical quality and ensure compliance in its late-stage clinical programs. This critical role includes managing GCP oversight, implementing quality strategies, and developing oversight plans while collaborating closely with various teams.

The ideal candidate will possess extensive GxP experience, strong communication skills, and the ability to thrive in a dynamic environment. A competitive salary range of $195,000 - $230,000 is offered for this pivotal position.