Regulatory Affairs Leader, Oncology Clinical Trials

McKesson Corporation; Florida; On-site; USD 140,000 - 200,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Senior Manager of Regulatory Affairs to oversee trial startup and ongoing compliance across multiple sites. You will partner with IRBs, sponsors, CROs, and internal teams to implement regulatory strategies and governance.

A strong background in regulatory operations, policy development, and team leadership is essential. Comprehensive Total Rewards are offered.

Qualifications

• Bachelor's degree required; Master’s preferred.
• Minimum 3 years of research regulatory experience on-site or within industry.
• Minimum 3 years of management experience with direct reports; CCRP/ACRP preferred.

Responsibilities

• Oversees regulatory start-up and maintenance of trials including safety and conflict of interest.
• Collaborates with study activation, protocol operations, budget, contracts, and finance teams.
• Develops/regulates policies for sites andClinical Operations teams; ensures compliance with FDA/GCP.

Skills

Regulatory leadership

Project management

Stakeholder collaboration

GCP/ FDA knowledge

People management

Education

Bachelor's degree

Master's degree preferred

Tools

Regulatory systems

IRB coordination

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Senior Manager of Regulatory Affairs to oversee trial startup and ongoing compliance across multiple sites. You will partner with IRBs, sponsors, CROs, and internal teams to implement regulatory strategies and governance.

A strong background in regulatory operations, policy development, and team leadership is essential. Comprehensive Total Rewards are offered.