myTomorrows
Healthcare
RegulatoryAffairsPharmacovigilanceManager
Neural analysis suggests this role is
optimal for Manager candidates.
“Regulatory Affairs Pharmacovigilance Manager at myTomorrows. Skills: Pharmacovigilance, Regulatory affairs, Risk management. Manage and oversee pharmacovigilance activities. Ensure compliance with global regulatory requirements”
Industry & Context.
Risk assessment; Signal detection
What They're Looking For.
Must Have
5+ years of experience in pharmacovigilance, Experience with regulatory submissions, Experience with GVP modules
Nice to Have
Experience in a biotech or pharmaceutical company, Experience with clinical development
What You'll Do.
Manage and oversee pharmacovigilance activities
Ensure compliance with global regulatory requirements
Develop and implement pharmacovigilance strategies
Conduct risk assessments and manage safety signals
Prepare and submit regulatory safety reports
Collaborate with internal and external stakeholders
Contribute to regulatory intelligence gathering
Maintain GVP modules and documentation
How You'll Work.
Team & Collaboration
Internal and external stakeholders
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). What you will do in this role: - Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals,
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