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 Programs. Support regulatory strategies for EAPs. Act as Regulatory Affairs expert”
Industry & Context.
Proactive problem solver; Identify regulatory challenges; Identify operational challenges; Suggest practical solutions
Reside within EST or CST
What They're Looking For.
Must Have
5 years relevant experience, Expanded Access experience, Working knowledge Pharmacovigilance, Bachelor's or Master's degree, Life Sciences degree, Experience with clients, Experience with external stakeholders
Nice to Have
Knowledge of additional languages
What You'll Do.
Support regulatory strategies for EAPs
Act as Regulatory Affairs expert
Act as Pharmacovigilance expert
Communicate with clients
Submit to Health Authorities
Attend cross-functional meetings
Prepare regulatory dossiers
Compile regulatory dossiers
Submit regulatory dossiers
Provide input for regulatory strategy
Ensure compliant handling
Handle regulatory activities
Handle pharmacovigilance activities
Stay up to date on regulations
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
Collaborate with Medical Affairs; Collaborate with Program Management; Collaborate with Quality Assurance; Collaborate with Supply Chain; Collaborate across teams; Work 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
Applying for this Regulatory Affairs Pharmacovigilance Manager role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Ashby
- Ashby is a fast modern ATS — most applications take under 3 minutes.
- The resume parser is strong; verify parsed experience dates and job titles.
- Custom screening questions are often scored algorithmically — answer completely.
- Location field affects geo-based screening; use your actual metro area.
ANONYMOUS · UNFILTERED
What do employees actually say about myTomorrows?
Real rants from real employees. Read before you apply.