Regulatory Affairs Analyst Jobs in Tennessee
Regulatory affairs analyst jobs in Tennessee are concentrated in Nashville, Memphis, and the Knoxville corridor, where healthcare, pharmaceuticals, and medical device manufacturing drive consistent demand at every level from junior specialist to senior compliance lead. Major employers with long-standing operations in the state include HCA Healthcare, Vanderbilt University Medical Center, and Cigna, all of which maintain regulatory and compliance functions that hire analysts regularly. The most in-demand specialties are FDA regulatory submissions, healthcare compliance, and pharmaceutical quality systems. See the openings below and apply to the ones that match your experience.
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Showing 5 of 7+ Regulatory Affairs Analyst jobs
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.
As the Regulatory Coordinator you are responsible for managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. In this position you will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.
- You will process regulatory document signature request through an electronic signature platform
- You will track documents pending site regulatory signatures
- You will provide site level regulatory support to the Clinical Operations’ sites and internal department managers in relation to the status of start-up and ongoing regulatory maintenance
- You will establish and maintain a document management system for regulatory paper and electronic files
- You will maintain Food and Drug Administration (FDA) and Good Clinical Practice (GCP) required regulatory documentation for individual sites, studies, sponsors and/or other networks. You will ensure all regulatory documentation is compliant with local Standard Operating Procedures (SOP’s) for format and content
- You will maintain updated physician credentials for network participants and other critical documentation ensuring compliance You will triage site requests for regulatory support and identifies correct pathway for issue resolution
You should have for this position:
- An Associate Degree, preferably a Bachelor’s Degree
- Regulatory experience is preferred Customer service experience is preferred
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.
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.
McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
McKesson job postings are posted on our career site: careers.mckesson.com .
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.
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.
As the Regulatory Coordinator you are responsible for managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. In this position you will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.
- You will process regulatory document signature request through an electronic signature platform
- You will track documents pending site regulatory signatures
- You will provide site level regulatory support to the Clinical Operations’ sites and internal department managers in relation to the status of start-up and ongoing regulatory maintenance
- You will establish and maintain a document management system for regulatory paper and electronic files
- You will maintain Food and Drug Administration (FDA) and Good Clinical Practice (GCP) required regulatory documentation for individual sites, studies, sponsors and/or other networks. You will ensure all regulatory documentation is compliant with local Standard Operating Procedures (SOP’s) for format and content
- You will maintain updated physician credentials for network participants and other critical documentation ensuring compliance You will triage site requests for regulatory support and identifies correct pathway for issue resolution
You should have for this position:
- An Associate Degree, preferably a Bachelor’s Degree
- Regulatory experience is preferred Customer service experience is preferred
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.
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.
McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.
McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
McKesson job postings are posted on our career site: careers.mckesson.com .
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.
See All 7 Regulatory Affairs Analyst Jobs in Tennessee
Find roles in Tennessee that match your experience and apply in just a few clicks.
Find JobsRegulatory Affairs Analyst Jobs by City in Tennessee
Where Tennessee roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Tennessee
A snapshot from current Tennessee openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
What Tennessee Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Tennessee.
- Bachelor's degree in life sciences, pharmacy, chemistry, or a closely related field
- Familiarity with FDA regulations, CFR Title 21, and federal regulatory submission processes
- Experience preparing or reviewing regulatory documents such as INDs, NDAs, or 510(k)s
- Knowledge of quality management systems and GxP compliance standards
- Proficiency with regulatory information management software and document control platforms
- Strong technical writing skills with the ability to communicate complex compliance requirements
Regulatory Affairs Analyst Jobs in Tennessee: Frequently Asked Questions
How do you become a regulatory affairs analyst in Tennessee?
Most regulatory affairs analyst roles in Tennessee require a bachelor's degree in a life science, pharmacy, or engineering discipline as the baseline entry point. Tennessee does not issue a state-specific regulatory affairs license, but employers in Nashville and Memphis strongly favor candidates who hold or are pursuing the Regulatory Affairs Certification from the Regulatory Affairs Professionals Society. Building experience through quality assurance, clinical research, or compliance roles at Tennessee's large health systems or pharmaceutical manufacturers is the most direct path.
Which companies hire regulatory affairs analysts in Tennessee?
Companies currently hiring regulatory affairs analysts in Tennessee include Sarah Cannon Research Institute, Opella., and McKesson, per current listings on Migrate Mate as of November 2026. Tennessee's concentration of hospital systems, managed care organizations, and pharmaceutical operations means demand is spread across both large corporate compliance teams and specialized regulatory consulting firms headquartered in the Nashville area.
Which Tennessee cities have the most regulatory affairs analyst jobs?
Tennessee, Bartlett, and Nashville account for the largest share of regulatory affairs analyst openings in Tennessee. Nashville dominates because it is home to a dense cluster of healthcare corporations, insurance companies, and pharmaceutical firms, while Memphis draws openings through its hospital networks and biomedical research institutions, and Knoxville adds openings tied to its medical device and manufacturing sector.
Are there remote regulatory affairs analyst jobs in Tennessee?
Yes, and more than most fields, because regulatory affairs work is primarily document-driven and does not require a physical presence on a production floor. About 0% of regulatory affairs analyst openings tied to Tennessee are remote or hybrid as of November 2026, reflecting how broadly employers have adopted flexible arrangements for compliance and submissions work. Document review, dossier preparation, and regulatory strategy roles are the most consistently offered in remote formats.
How can I get hired as a regulatory affairs analyst in Tennessee with little or no experience?
The most realistic entry path is moving laterally from a quality assurance, clinical research coordinator, or compliance specialist role at a Tennessee health system or pharmaceutical company. HCA Healthcare and Vanderbilt University Medical Center both run structured early-career programs in compliance and regulatory operations that serve as a pipeline for analyst positions. Earning the Regulatory Affairs Certification in Training designation from the Regulatory Affairs Professionals Society while in an adjacent role signals commitment and gives candidates a measurable edge with Tennessee employers.
Where can I find and apply to regulatory affairs analyst jobs in Tennessee?
You can find and apply to regulatory affairs analyst jobs in Tennessee on Migrate Mate, which lists current openings across the state. Search the listings, find the roles that match your background and location preference, and apply directly to the ones that fit.
See All 7 Regulatory Affairs Analyst Jobs in Tennessee
Find roles in Tennessee that match your experience and apply in just a few clicks.
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