Remote Associate Director of Regulatory Affairs Jobs
Remote Associate Director of Regulatory Affairs jobs are open across the U.S. at remote-first biotech, pharmaceutical, and medical device companies, as well as distributed teams in life sciences consulting and contract research organizations. Employers hiring remotely right now include Parexel, Pace Analytical Services, and Insmed Incorporated. See the openings below and apply to the ones that match your experience.
Find JobsOverview
Showing 5 of 99+ Remote Associate Director of Regulatory Affairs jobs









ABOUT THE ROLE:
We are seeking an articulate, thorough and highly organized individual who is results driven with a passion for risk mitigation. The Director of PBM Compliance and Regulatory Affairs will be a critical leader of Rightway's Compliance team. As a strategic member of the team, you will guide the integration of compliance obligations into the organization's operational, contractual, data, technology, and client-facing processes. You will provide leadership and oversight to promote continuous regulatory readiness, strengthen risk management practices, establish and maintain effective compliance controls, validate compliance through evidence-based reviews, and foster a proactive culture of compliance within a complex and rapidly evolving regulatory environment.
This role is instrumental in establishing a best in class compliance department and have the tactical skills to execute on the departmental needs through system integration, policy establishment and results monitoring.
WHAT YOU'LL DO:
- Perform federal and state regulatory research proactively anticipate business needs and requirements, identify and communicate potential risks/needs to key stakeholders, develop policies and procedures as well as strategic plans to mitigate risks and address needs
- Specific to business registration and licensure requirements, routinely conduct and monitor state and federal regulations, in addition, prepare, file and manage business registrations and licenses including the submission of required reporting
- Partner with department leads to ensure compliance with all statutory and regulatory requirements, pharmacy compliance activities and PBM compliance initiatives across the business; develop and maintain department approved regulatory and legislative compliance plan; create, implement, and maintain effective internal controls including policies and procedures
- Partner with department leads to ensure terms and conditions within vendor and client contracts as well as other pertinent agreements comply with applicable state and federal regulations
- Track, monitor and communicate across departments i) policies and procedures; ii) performance and reporting requirements; and iii) key metrics
- Participate as compliance subject matter expert on all mandated projects and escalated matters; achieve business operational compliance with all related measures relative to PBM accreditation initiatives
- Maintain an understanding and knowledge of regulatory affairs in all applicable jurisdictions and regulatory environments; lead and facilitate the development of company positions as well as internal and external responses related to pending regulatory initiatives
- Develop and implement training and communication plans; manage and lead scheduled and ad-hoc compliance projects; provide and deliver compliance consultation services to all departments
- Provide strategic compliance leadership and guidance to Rightway clients and business partners, fostering a culture of compliance, regulatory accountability, and operational excellence.
- Promote continuous improvement of regulatory programs and initiatives by identifying opportunities for improvement; work with key stakeholders across departments to design and implement regulatory process improvement programs and initiatives; and develop recommendations
- Conduct, direct, lead and facilitate all activities related to Internal and External (Regulatory and Client) audits and responses to findings
- Lead, mentor, and develop a team of compliance professionals and people leaders through coaching,performance management, succession planning, and talent development.
WHO YOU ARE:
- Education level: Bachelor's Degree Required (Preferred: Master's Degree) and JD (Juris Doctorate) degree or equivalent combination of practical experience
- Work experience: Minimum 7 years of relevant work experience in the healthcare industry with PBM industry experience preferred
- Important characteristics of ideal candidate: Detail-oriented, analytical, intellectually curious, good listener, empathetic, ability to challenge status quo, values exemplar
- Specific skills needed for job: Solid communication, research and organizational skills, ability to lead projects and influence others even without direct reporting line ownership
- Ability to work independently and manage multiple projects in a fast-paced, fluid environment
- Advanced computer and Windows skills required
COMPENSATION: $185,000 - $220,000 annually, in addition to bonus and equity
Compensation offered will be determined by geographic location, experience, and qualifications.
CYBERSECURITY AWARENESS NOTICE
In response to ongoing and industry-wide fraudulent recruitment activities (i.e., job scams), Rightway wants to inform potential candidates that we will only contact them from the @rightwayhealthcare.com email domain. We will never ask for bank details or deposits of any kind as a condition of employment.
ABOUT RIGHTWAY:
Rightway is on a mission to harmonize healthcare for everyone, everywhere. Our products guide patients to the best care and medications by inserting clinicians and pharmacists into a patient's care journey through a modern, mobile app. Rightway is a front door to healthcare, giving patients the tools they need along with on-demand access to Rightway health guides, human experts that answer their questions and manage the frustrating parts of healthcare for them.
Since its founding in 2017, Rightway has raised over $300mm from investors including Khosla Ventures, Thrive Capital, Francisco Partners, and Tiger Global. We're headquartered in New York City, with satellite offices in Denver and Dallas. Our clients rely on us to transform the healthcare experience, improve outcomes for their teams, and decrease their healthcare costs.
HOW WE LIVE OUR VALUES TO OUR TEAMMATES:
We're seeking those with passion for healthcare and relentless devotion to our goal. We need team members that embody our core values:
1) We are human, first
Our humanity binds us together. We bring the same empathetic approach to every individual we engage with, whether it be our members, our clients, or each other. We are all worthy of respect and understanding and we engage in our interactions with care and intention. We honor our stories. We listen to—and hear—each other, we celebrate our differences and similarities, we are present for each other, and we strive for mutual understanding.
2) We redefine what is possible
We always look beyond the obstacles in front of us to imagine new solutions. We approach our work with inspiration from other industries, other leaders, and other challenges. We use ingenuity and resourcefulness when faced with tough problems.
3) We debate then commit
We believe that a spirit of open discourse is part of a healthy culture. We understand and appreciate different perspectives and we challenge our assumptions. When working toward a decision or a new solution, we actively listen to one another, approach it with a "yes, and" mentality, and assume positive intent. Once a decision is made, we align and champion it as one team.
4) We cultivate grit
Changing healthcare doesn't happen overnight. We reflect and learn from challenges and approach the future with a determination to strive for better. In the face of daunting situations, we value persistence. We embrace failure as a stepping stone to future success. On this journey, we seek to act with guts, resilience, initiative, and tenacity.
5) We seek to delight
Healthcare is complicated and personal. We work tirelessly to meet the goals of our clients while also delivering the best experience to our members. We recognize that no matter the role or team, we each play a crucial part in our members' care and take that responsibility seriously. When faced with an obstacle, we are kind, respectful, and solution-oriented in our approach. We hold ourselves accountable to our clients and our members' success.
Rightway is proud to be an Equal Opportunity Employer that believes in the strength of diverse thought, beliefs, backgrounds, and education. We foster an inclusive culture where differences are celebrated to drive the best business decisions possible. We do not discriminate on any basis protected by applicable law. All employment decisions are based on merit, qualifications, need, and performance.
See All 99 Remote Associate Director of Regulatory Affairs Jobs
Find roles that match your experience and apply in just a few clicks.
Find JobsRemote Associate Director of Regulatory Affairs Job Market
Who's Hiring



Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Medical Devices
- Banking & Financial Services
- Consulting & Professional Services
What Employers Look For
The qualifications that appear most often in remote associate director of regulatory affairs jobs.
- Bachelor's or advanced degree in life sciences, pharmacy, chemistry, or a related field
- Minimum five to eight years of regulatory affairs experience in pharmaceutical or biotech settings
- Hands-on experience preparing and submitting INDs, NDAs, BLAs, or 510(k)s to the FDA
- Working knowledge of ICH guidelines, 21 CFR regulations, and eCTD submission standards
- RAC certification from the Regulatory Affairs Professionals Society preferred or required
- Experience using regulatory information management systems such as Veeva Vault or similar platforms
Tips for Your Remote Associate Director of Regulatory Affairs Job Search
Signal async regulatory experience upfront
Remote regulatory teams depend on written communication over real-time meetings. Highlight experience writing clear regulatory strategy memos, managing submission timelines asynchronously, and coordinating with cross-functional teams across time zones without needing frequent check-ins.
Find remote openings in one place
Migrate Mate lists remote associate director of regulatory affairs openings from companies across the U.S. in one place. Search roles that match your regulatory background and apply directly to the ones that fit your experience and preferred industry sector.
Show ownership of past regulatory submissions
Remote employers can't observe your day-to-day work, so your application needs to prove independent ownership. Name the specific submission types you've led, the agencies you've interfaced with, and the outcomes you drove without close supervision from senior staff.
Prepare for remote-format regulatory interviews
Remote interviews for this role often include scenario questions about managing agency interactions, resolving submission gaps, and coordinating distributed teams. Practice giving structured answers that show regulatory judgment and clear written and verbal communication under time pressure.
Remote Associate Director of Regulatory Affairs Jobs: Frequently Asked Questions
How do I get a remote associate director of regulatory affairs job?
Target remote-first biotech and pharmaceutical companies, contract research organizations, and medical device firms with distributed regulatory teams, since these employers are most likely to hire this role remotely. Remote hiring managers screen for independent judgment, strong written communication for async collaboration, and deep familiarity with FDA submission processes and regulatory strategy. Demonstrating a history of managing cross-functional projects without direct oversight gives you a clear edge.
Which companies hire remote associate director of regulatory affairss?
Remote associate director of regulatory affairs roles are posted by Parexel, Pace Analytical Services, and Insmed Incorporated and others right now, based on current remote listings on Migrate Mate as of November 2026. These include remote-first biotech and pharmaceutical companies, distributed contract research organizations, and medical device firms that run regulatory functions across geographically dispersed teams.
Can you get a remote associate director of regulatory affairs job with no experience?
Yes, but remote associate director of regulatory affairs roles at this seniority level are rarely entry-level, so candidates without direct regulatory leadership experience face a steep climb. Your strongest path is building regulatory experience in on-site or hybrid roles first, then transitioning remotely. Demonstrating async project management skills, FDA or EMA knowledge, and self-directed deliverables can help open doors with smaller remote-first companies.
Do you need a degree for remote associate director of regulatory affairs jobs?
Usually, but the degree matters less than the regulatory expertise behind it. Most remote employers expect at least a bachelor's degree in a life sciences field, and many prefer a graduate degree for director-level roles. However, candidates who can show deep hands-on experience with submissions, dossiers, and agency interactions often move forward even if their academic background is not an exact match.
Which industries hire the most remote associate director of regulatory affairss?
The sectors hiring the most remote associate director of regulatory affairss are Biotechnology & Pharmaceuticals, Medical Devices, and Banking & Financial Services, based on current remote listings on Migrate Mate as of November 2026. These industries rely on distributed regulatory teams to manage submissions, compliance timelines, and agency relationships across multiple sites and time zones.
See All 99 Remote Associate Director of Regulatory Affairs Jobs
Find roles that match your experience and apply in just a few clicks.
Find Jobs