Regulatory Affairs Manager – Expanded Access Programs

🔥 8 minutes ago

🏄 California, New York – Remote

🏄 California – Remote 🗽 New York – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

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myTomorrows

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2012

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 Venture Round on 2017-01

Biotechnology • Healthcare Insurance • Pharmaceuticals

myTomorrows is a healthcare company dedicated to helping patients discover and access experimental treatments through clinical trials and expanded access programs. They provide personalized patient navigation and support to empower patients and their families in making informed decisions regarding their treatment journeys. By leveraging technology and partnerships with healthcare professionals and biopharmaceutical companies, myTomorrows aims to bridge the gap between patients and innovative therapies currently in development.

📋 Description

• Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs. • Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits. • Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients. • Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how). • Collaborate with the Commercial team to support new EAPs. • Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs. • Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs. • Assist in drafting, reviewing, and maintaining regulatory documentation and templates. • Liaise with the Pharmacovigilance service provider to ensure alignment and compliance. • Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions).

🎯 Requirements

• Approximately 5 years of relevant experience in Regulatory Affairs, including experience in Expanded Access. • Working knowledge of fundamental principles of Pharmacovigilance is required. • Solid understanding of national and international legislation and regulation relating to Expanded Access. • A Bachelor’s or Master's degree in Life Sciences or a related field. • Experience working directly with clients or external stakeholders in a professional setting. • Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus. • Comfortable collaborating across teams and working in a cross-functional environment. • Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions. • Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint).

🏖️ Benefits

• Impactful work that helps patients gain access to potentially lifesaving treatments. • International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability. • Competitive salary, annual performance bonus and an Employee Stock Option Plan. • Great career development opportunities in a fast-growing company. • Learning and development budget alongside internal knowledge sharing sessions. • Hybrid working model if you're in the Netherlands. • Policies to support working parents. • Healthy lunch at the thriving Amsterdam office. • Unlimited access to professional guidance by certified psychologists via OpenUp. • Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration!