20 beste vacatures voor de functie van clinical trial in amsterdam (nieuwe medewerkers gezocht)

Regulatory Affairs Manager (Expanded Access Programs)
myTomorrows —Amsterdam
- Fulltime
- Hybride werken
- Microsoft Word
- Microsoft Excel
- Engels
(Ervaren) Clinical Project Manager (CPM)
Antoni van Leeuwenhoek —Amsterdam
- € 3.903 - € 5.503 per maand
- Online sollicitatie
- Ziekenhuis
- Engels
- Onderzoek
- Kosteloos parkeren
- Reiskostenvergoeding
Snel solliciteren
Global Health Economics and Outcome Research - VIE Contract
Sanofi —Amsterdam
- Microsoft Excel
- Doctor
- Engels
13 dagen
Onderzoeksarts Amsterdam, Zwolle en Den Bosch
Progress Clinical Research en Brain Research Center —Amsterdam Zuid
- € 4.120 - € 6.180 per maand
- Parttime
- Laboratorium
- Reiskostenvergoeding
Sr. Clinical Project Manager (Europe)
Allucent —Amsterdam
- Hybride werken
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Budget voor professionele ontwikkeling
- Flexibele werkuren
Snel solliciteren
Clinical Data Management Lead
IQVIA —Amsterdam
- Fulltime
- Thuiswerk
- Oracle
- Onderzoek
- Managementervaring
Executive Director of Clinical Business Development (Strategic Accounts)
Syneos Health Commercial Solutions —Amsterdam
- Doctor
- Verkoopervaring
- Salesforce
Customer Success Specialist (EMEA)
Nicolab —Amsterdam-Zuidoost
- € 45.000 - € 75.000 per jaar
- Parttime
- Ziekenhuis
- Engels
- Onderzoek
- Flexibele werkuren
- Aanbrengbonus
Snel solliciteren
Student onderzoeksassistent GRIPonMASH-studie: Europese studie naar leverfibrose
Amsterdam UMC —Amsterdam-Zuidoost
- € 17,59 per uur
- Parttime
- Geneeskunde
- Communicatieve vaardigheden
7 dagen
Onderzoeksarts
Progress Clinical Research en Brain Research Center —Amsterdam Zuid
- € 4.120 - € 6.180 per maand
- Parttime
- Laboratorium
- Reiskostenvergoeding
Senior Medical Science Liaison (FTC)
Vertex Pharmaceuticals —Haarlem
- Fulltime
- Engels
- Microsoft Office
- Master
Associate Director, Oncology Distribution – Europe
Corcept Therapeutics —Amsterdam
- € 110.000 - € 125.000 per jaar
- Bachelor
Snel solliciteren
Legal Counsel
4G Clinical, LLC —Amsterdam Centrum
- Engels
- Master
- Analytisch vermogen
Snel solliciteren
Data Standards Engineer (CDISC)
IQVIA —Amsterdam
- Fulltime
- Informatica
- Java
- Bachelor
Principal Biostatistician (Oncology) - FSP
IQVIA —Amsterdam
- Fulltime
- Bediening
- Communicatieve vaardigheden
1 dag
Manager, Medical Affairs
Gilead Sciences —Amsterdam
- Fulltime
- Geneeskunde
- Doctor
- Verkoopervaring
3 uur
Account Manager Vascular Access Management: Zuid West NL
BD —Amsterdam
- € 58.800 - € 89.700 per jaar
- Verkoopervaring
- Ziekenhuis
- Engels
10 uur
Director, Site Head Operations
uniQure —Amsterdam
- Engineering
- ERP systemen
- Engels
Account Executive (BDA) - Amsterdam
Ideals —Amsterdam
- Fulltime
- Hybride werken
- Verkoopervaring
- Engels
- Communicatieve vaardigheden
Technical Product Owner
myTomorrows —Amsterdam
- Fulltime
- Hybride werken
- Azure
- Engels
- AWS

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Regulatory Affairs Manager (Expanded Access Programs)

myTomorrows
Amsterdam

Nu solliciteren

Vacaturegegevens

Fulltime

Kwalificaties

Microsoft Word
Microsoft Excel
Supplychain
Engels
Master
SharePoint
Gegevensverzameling
Communicatieve vaardigheden

Volledige vacaturetekst

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, 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).

What you bring to the table:

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)

What we offer:

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!

Equal opportunities

myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that.

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clinical trial vacatures in amsterdam

Regulatory Affairs Manager (Expanded Access Programs)

(Ervaren) Clinical Project Manager (CPM)

Global Health Economics and Outcome Research - VIE Contract

Onderzoeksarts Amsterdam, Zwolle en Den Bosch

Sr. Clinical Project Manager (Europe)

Clinical Data Management Lead

Executive Director of Clinical Business Development (Strategic Accounts)

Customer Success Specialist (EMEA)

Student onderzoeksassistent GRIPonMASH-studie: Europese studie naar leverfibrose

Onderzoeksarts

Senior Medical Science Liaison (FTC)

Associate Director, Oncology Distribution – Europe

Legal Counsel

Data Standards Engineer (CDISC)

Principal Biostatistician (Oncology) - FSP

Manager, Medical Affairs

Account Manager Vascular Access Management: Zuid West NL

Director, Site Head Operations

Account Executive (BDA) - Amsterdam

Technical Product Owner

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical trial in amsterdam

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