20 beste vacatures voor de functie van gcp in 2549 den haag (nieuwe medewerkers gezocht)

Associate Director Biostatistics
ProQR Therapeutics —Leiden
- Fulltime
- Doctor
- Engels
- Onderzoek
11 dagen
Senior QA Manager
Cerba Research —Rotterdam
- Fulltime
- Laboratoriumervaring
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- Analytisch vermogen
Snel solliciteren
12 dagen
Software Engineer
Lionsville —Den Haag
- € 5.400 - € 6.950 per maand
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- Azure
- Java
- SQL
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B2B Integration Engineer (TypeScript & Azure)
Eneco —Rotterdam
- € 79.000 - € 108.000 per jaar
- Hybride werken
- Azure
- DevOps
- AWS
- Winstdeling
- Werk vanuit huis
6 dagen
Technical Architect / Senior Fullstack Developer
DotControl —Rotterdam
- € 4.800 - € 5.800 per maand
- Parttime
- Azure
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- Kantoor
DevOps Engineer
FreshMinds —Leiden
- € 80.000 - € 155.000 per jaar
- Fulltime
- Hybride werken
- Azure
- DevOps
- Kantoor
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Technical Lead - Merch Platform & ERP - Fast Growing Scale Up
Monday Merch —Rotterdam
- Vanaf € 6.000 per maand
- Fulltime
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- ERP systemen
- Bachelor
- Begeleiding
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Import & Export Compliance Officer
Cerba Research —Rijswijk
- Fulltime
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- Engels
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- Zonder diploma
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Backend Developer Golang
Payter B.V. —Rotterdam
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- Engels
- Java
- Databases
- Reiskostenvergoeding
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Platform Automation Engineer
LessonUp —Den Haag
- € 5.000 - € 6.000 per maand
- Fulltime
- Hybride werken
- DevOps
- Bachelor
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- Budget voor professionele ontwikkeling
Snel solliciteren
10 dagen
IoT / DevOps Engineer - Home Energy Management
Eneco —Rotterdam
- € 69.000 - € 100.000 per jaar
- Hybride werken
- Azure
- DevOps
- Engineering
- Winstdeling
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6 dagen
Transport Network Coordinator
Cerba Research —Rijswijk
- Fulltime
- Engels
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Senior Data Engineer
Good Company —Leiden
- Online sollicitatie
- Azure
- SQL
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Technical Information Security Officer
ANWB —Den Haag
- € 4.710 - € 7.627 per maand
- Hybride werken
- Azure
- ICT
- Communicatieve vaardigheden
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GTM & CoE Lead, Insights & Data
Capgemini —Rotterdam
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Data Science Consultant
Sia —Rotterdam
- Fulltime
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AI Consultant - Utilities & Water
CGI —Rotterdam
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Junior DevOps Engineer
[email protected] —Zoetermeer
- Fulltime
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Medior/Senior Data Engineer (32+ uur), Den Bosch
Data Rocks —Rotterdam
- € 4.000 - € 6.500 per maand
- Parttime
- Hybride werken
- Azure
- Engels
- SQL
- Flexibele werkuren
IoT & DevOps Engineer (TypeScript & Azure)
Eneco —Rotterdam
- € 79.000 - € 108.000 per jaar
- Hybride werken
- Azure
- DevOps
- AWS
- Winstdeling
- Werk vanuit huis
6 dagen

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Associate Director Biostatistics

ProQR Therapeutics
Leiden

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Vacaturegegevens

Fulltime
11 dagen geleden

Secundaire arbeidsvoorwaarden

Aandelenopties
Pensioen

Kwalificaties

Statistiek
Doctor
R
Wiskunde
Engels
Onderzoek
Master
Analytisch vermogen
Python

Volledige vacaturetekst

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA.
At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering transformative RNA therapies to make a difference in the lives of the communities we serve.

Our proprietary Axiomer™ RNA editing technology platform enables the editing of specific single nucleotides in RNA using the cells own editing machinery. Axiomer RNA editing technology harnesses ADAR (Adenosine Deaminase Acting on RNA), a protein which is present in all human cells, to repair G-to-A mutations, modulate protein, and enable protective mutation functions. Axiomer could potentially yield a new class of innovative medicines and treat currently untreatable diseases. By harnessing the power of RNA editing, we aim to create a world where genetics inform your health - but never limit it.

Our Development / Clinical Quantitative Science department is currently looking for an Associate Director Biostatistics (Full-time) to join our team.

Location: Leiden, the Netherlands (on-site).

The Role
As Associate Director Biostatistics, you will provide senior statistical leadership across clinical and translational programs. This is a hands-on, high-autonomy role with strong matrix leadership: you will shape quantitative strategy, guide study design and analysis, oversee complex computational work, and help teams make clear, evidence-based decisions.

You will work closely with Clinical Development, Clinical Operations, Data Management, Biomarkers, Regulatory, external partners, CROs, and senior stakeholders. The role requires critical thinking, scientific maturity, strong communication, and the ability to operate pragmatically in a fast-moving biotech environment.

What You Will Do

Serve as biostatistical lead for clinical and translational projects, including protocol design, endpoints, estimands, sample size, SAPs, TLFs, interim/adaptive decisions, reporting, and regulatory responses.
Develop and defend quantitative strategies using frequentist and Bayesian methods, simulation, leveraging external evidence, sensitivity analyses, and decision-focused interpretation.
Plan, oversee, monitor, QC, and document demanding computational work, ensuring reproducibility, traceability, and fit-for-purpose quality.
Contribute to clinical development strategy by translating biological, clinical, regulatory, and operational questions into robust statistical plans.
Author and review statistical sections of protocols, synopses, briefing books, CSRs, regulatory documents, internal decision memos, and presentations.
Oversee CROs, consultants, programmers, and analytical vendors to ensure timelines, quality, documentation, and audit readiness.
Support GCP-aware ways of working and contribute to statistical quality systems, clinical data infrastructure, and good documentation practice.
Identify statistical, data, interpretability, and operational risks early, and propose pragmatic mitigation options.
Mentor colleagues in a matrix setting and promote quality, scientific challenge, and clear communication.

We expect our Associate Director Biostatistics to have:

PhD or MSc in biostatistics, statistics, mathematics, data science, epidemiology, or a related quantitative discipline.
At least 5 years of relevant experience (3+ if PhD.) in biotech, pharma, CRO, academic clinical research, or a comparable setting.
Experience leading statistical work for clinical studies, ideally including rare disease, small populations, translational medicine, precision medicine, or innovative trial designs.
Strong command of R is required. Python is a clear plus. SAS is useful but not mandatory.
Good command of Bayesian models, Bayesian thinking, adaptive or innovative designs, and simulation-based planning.
Ability to design and critically review complex analyses, not just execute them.
Familiarity with cloud or controlled computation environments, reproducible workflows, version control, and data-science techniques.
Knowledge of GCP and experience with regulatory interactions are strong pluses.
Strong written and verbal communication in English.
High integrity, quality mindset, pragmatic problem-solving, and the confidence to challenge assumptions constructively.

Skills and competencies that are required for making the difference:

We are looking for someone who combines statistical depth with strategic judgement. You are comfortable working independently, but you also know how to bring people with you. You can move between hands-on analysis, study-level statistical leadership, and senior stakeholder discussion. You communicate proactively, clearly, respectfully, and fearlessly.

If this role sounds exciting but you do not meet every criterion, we would still like to hear from you. Some gaps can be closed by doing the work; critical thinking, ownership, quality, and willingness to learn are essential.

ProQR as an employer

As an employer, we value a diverse workforce in which people are encouraged to develop themselves both personally and professionally. We believe that when people are happy, energized and supported by an environment in which they can thrive, they can achieve extraordinary things.

We are committed to ensuring that no employee, candidate, or job applicant receives less favorable treatment on the grounds of race, age, disability, pregnancy, religion, gender identity and expression, sexual orientation, marriage or civil partnership status. At ProQR we want to create an inclusive culture where everyone can be valued for who they are and in which individual differences and contributions in all forms are recognized and valued.

We offer an exciting and innovative working environment in a very committed organization, with the following benefits:

8% holiday allowance

30 vacation days

An annual performance bonus

Stock options

A premium-free pension plan

A commuting allowance

A subsidized staff restaurant

Unlimited (un)healthy snacks and drinks

Employee events (boot camp, Coffee and Collaboration Café and other social events)

We are looking for people who are inspired by our mission to edit RNA, treat disease and change lives. Are you up for the challenge?

Please contact Silvia Catellani via [email protected] if you have any questions.

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gcp vacatures in 2549 den haag

Associate Director Biostatistics

Senior QA Manager

Software Engineer

B2B Integration Engineer (TypeScript & Azure)

Technical Architect / Senior Fullstack Developer

DevOps Engineer

Technical Lead - Merch Platform & ERP - Fast Growing Scale Up

Import & Export Compliance Officer

Backend Developer Golang

Platform Automation Engineer

IoT / DevOps Engineer - Home Energy Management

Transport Network Coordinator

Senior Data Engineer

Technical Information Security Officer

GTM & CoE Lead, Insights & Data

Data Science Consultant

AI Consultant - Utilities & Water

Junior DevOps Engineer

Medior/Senior Data Engineer (32+ uur), Den Bosch

IoT & DevOps Engineer (TypeScript & Azure)

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van gcp in 2549 den haag

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