Manager of Regulatory Affairs - Remote US

Sarah Cannon Research Institute; United States; Remote; USD 120,000 - 170,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization with a nationwide network of clinical trials. This remote role oversees the regulatory operations for site Clinical Operations, ensuring FDA/GCP compliance and audit readiness while aligning with strategic plans and cross-functional partners.

The Regulatory Affairs Manager will lead regulatory policies, manage sponsor relationships, and coordinate with primary investigators and industry sponsors to support trial

Qualifications

• Bachelor’s Degree required.
• 1+ year work experience with 5+ years’ preferred in clinical research corporation and regulatory team; education may substitute partially.
• Knowledge of scientific and clinical research terminology.
• Knowledge of FDA and GCP guidelines.
• Knowledge of organizational policies, procedures, and systems.
• Advanced skills with MS Office products including Excel, Word, Outlook.
• Experience meeting strict deadlines and supervising team members.

Responsibilities

• Manages regulatory department activities and schedules.
• Establishes and enforces procedures ensuring trial teams/sites comply with laws, regulations, SOPs, and guidelines.
• Develops and implements regulatory policies for site operations and Clinical Operations team.
• Manages regulatory affairs between the organization for multiple clinical trials according to FDA and GCP.
• Oversees regulatory audits by sponsors/industry and governmental auditors.
• Other duties as assigned.

Skills

Regulatory affairs

FDA guidelines

GCP guidelines

Team supervision

Clinical research terminology

Education

Bachelor's Degree

Tools

MS Office

Job description

It’s More Than a Career, It’s a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.

Our Regulatory Affairs Manager oversees all aspects of the regulatory operations for Sarah Cannon site Clinical Operations and manages the regulatory department. This position is responsible for developing and implementing short‑and‑long‑term strategies for the regulatory compliance for the site Clinical Operations. You will ensure Sarah Cannon adheres to and maintains FDA regulatory compliance as well as oversees any regulatory audit. This position will work closely with the department directors and/or primary investigators, industry sponsors and other outside entities.

_ This is a remote position based in the US; relocation assistance and visa sponsorship are not available. _

Duties include and are not limited to:

• Manages, directs, plans and schedules activities and programs for the regulatory department
• Establishes and enforces procedures that assure all trial teams and sites are fully compliant with all applicable laws, regulations, SOPs, and other applicable guidelines
• Develops and implements regulatory policies and procedures for the sites and the site Clinical Operations team, including managing and planning regulatory affairs compliance for industry sponsors and/or sites
• Manages the regulatory affairs between the organization for multiple clinical trials according to FDA and GCP guidelines; for individual sites, studies, sponsors and/or other networks
• Manages the relationships between industry partners and the FDA regarding regulatory compliance for the organization and managing regulatory audits of studies by sponsor/industry and governmental auditors.
• Other duties as assigned

Qualifications for success include :

• Bachelor’s Degree
• 1+ year work experience with 5+ years’ preferred in clinical research corporation and regulatory team - education may be substituted for partial experience
• Knowledge of scientific and clinical research terminology
• Knowledge of FDA and GCP guidelines
• Knowledge of organizational policies, procedures, and systems
• Advanced skills with MS Office products including Excel, Word, Outlook
• Experience meeting strict deadlines and supervising team members

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first‑in‑human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.

We care about the well‑being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well‑being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please...

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.