myTomorrows
Healthcare
RegulatoryAffairsPharmacovigilanceManager
Neural analysis suggests this role is
optimal for Manager candidates.
“Regulatory Affairs Pharmacovigilance Manager at myTomorrows. Skills: Regulatory Affairs, Pharmacovigilance, Expanded Access. Support regulatory strategies for EAPs. Act as RA/PV expert”
Industry & Context.
Identify challenges; Suggest solutions
What They're Looking For.
Must Have
5 years relevant experience, Expanded Access experience, Working knowledge of Pharmacovigilance, Bachelor's or Master's degree, Experience with clients/external stakeholders, Reside within EST or CST time zones
Nice to Have
Knowledge of additional languages
What You'll Do.
Support regulatory strategies for EAPs
Communicate with clients
Submit to Health Authorities
Attend cross-functional meetings
Prepare regulatory dossiers for EAPs
Compile regulatory dossiers for EAPs
Submit regulatory dossiers for EAPs
Provide input for regulatory strategy
Support setting up EAPs
Support executing EAPs
Collaborate with Commercial team
Ensure compliant handling of regulatory activities
Ensure compliant handling of pharmacovigilance activities
Stay up to date on global laws
Stay up to date on regulations
Stay up to date on guidelines
Assist in drafting documentation
Assist in reviewing documentation
Assist in maintaining documentation
Liaise with Pharmacovigilance provider
Contribute to maintaining SOPs
Contribute to maintaining QIs
Contribute to maintaining CAPAs
How You'll Work.
Team & Collaboration
Working with Medical Affairs; Working with Program Management; Working with Quality Assurance; Working with Supply Chain; Collaborating across teams; Working in cross-functional environment
Communication Scope
Convey complex topics
Full Job Description
About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem. We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection. With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business. Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Regulatory Affairs & Pharmacovigilance Manager As the Regulatory Affairs and Pharmacovigilance Manager, you will be responsible for ensuring compliance of our processes with country-specific expanded access regulations globally. In this role, you'll be a key contributor to our regulatory and quality infrastructure, keeping us aligned with global legislation. You will be actively working together with Medical Affairs, Program Management, Quality Assurance, and Supply Chain and will report to the Director of Regulatory Affairs and Pharmacovigilance (Emily says hi). Geographic Requirement: For candidates in North America, to ensure seamless collaboration with our teams, applicants must reside within the EST or CST time
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