20 beste Stellen als clinical research in nordrhein westfalen – aktuell auf Personalsuche

Clinical Research Associate (CRA) (m/f/d), full-time
phenox GmbH —Bochum
- Vollzeit
- Hybrides Arbeiten
- Nursing
- Englisch
- Forschungserfahrung
Research Assistant / Clinical Reserach Coordinator (m/w/d)
Profil Institut für Stoffwechselforschung GmbH —Neuss
- 4.000 € – 4.400 € pro Monat
- Per E-Mail
- Englisch
- Forschungserfahrung
- Personalführung
- Kostenloser Parkplatz
- Gleitzeit
Direkt bewerben
13 Tage
Sr. Clinical Research Associate (Germany)
Allucent —Köln
- Vollzeit
- Hybrides Arbeiten
- Bachelor
- Mit Reiseanteil
- Flexible Arbeitszeiten
- Empfehlungsprogramm
Direkt bewerben
Clinical Research Associate (f/m/d) EMEA
Zoll Medical Corporation —Köln
- Vollzeit
- Microsoft Word
- Microsoft Excel
- Doktorat
- Employee Assistance Program
- Flexible Arbeitszeiten
Clinical Research Associate (m/w/d)
Universitätsklinikum Essen —Essen
- Vollzeit
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Weiterbildungsprogramme
13 Tage
Senior Clinical Project Manager (m/w/d), full-time
phenox GmbH —Bochum
- Vollzeit
- Hybrides Arbeiten
- Nursing
- Forschungserfahrung
- Master
Supervisor, Clinical Trial Materials
LabConnect, LLC —Köln
- ERP-Systeme
- Microsoft Office
- Hochschulreife
Direkt bewerben
Research Position (PhD Position) (m/f/d)
Universität Bielefeld —Bielefeld
- Teilzeit
- Datenanalyse
- Master
- Machine Learning
- Flexible Arbeitszeiten
Leiter*in (m/w/d) Koordinierungsstelle Klinische Studien / Clinical Research Support Unit
Universität Bielefeld —Bielefeld
- Online-Bewerbung
- Microsoft Powerpoint
- Doktorat
- Englisch
- Homeoffice-Möglichkeit
- Weiterbildungsprogramme
Biobank - Pre Clinical Research Assistant (m/w/d)
QIMA —Münster
- Vollzeit
- Englisch
- Bachelor
- Gleitzeit
- Flexible Arbeitszeiten
Direkt bewerben
11 Tage
PhD Candidate (f/m/x) in Ophthalmic Epidemiology
Deutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE) —Bonn
- Vollzeit
- Doktorat
- Forschungserfahrung
- Master
- Flexible Arbeitszeiten
Research Position (m/f/d) - Experimental Endocrinology and Tumor cell metabolism
Universität Bielefeld —Bielefeld
- Vollzeit
- Doktorat
- Personalführung
13 Tage
Research Assistant / Clinical Research Coordinator (m/w/d)
Profil Institut für Stoffwechselforschung GmbH —Neuss
- Per E-Mail
- Englisch
- Forschungserfahrung
- Erfahrung in der IT
- Employee Assistance Program
- Weiterbildungsprogramme
7 Tage
Clinical Trial Materials Specialist I
LabConnect, LLC —Köln
- Hochschulreife
- Mathematikkenntnisse
Direkt bewerben
Scientist in-vitro Pharmacology (m/f/d)
Grünenthal —Aachen
- Vollzeit
- Doktorat
- Datenanalyse
PhD candidate (m/f/x) in the Research Training Group “Monoaminergic Neuronal Networks & Disease” – Mechanistic aspects of GPCR signaling
Ruhr Universität Bochum —Bochum
- Teilzeit
- Forschungserfahrung
- Master
- Sprachkenntnisse werden vermittelt
7 Tage
Research Technician (m/f/d) – full time
QIMA —Münster
- Vollzeit
- Englisch
- Forschungserfahrung
- Microsoft Office
- Flexible Arbeitszeiten
Direkt bewerben
11 Std.
PhD Candidate (m/f/d)
Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. —Dortmund
- 4.768,12 € pro Monat
- Vollzeit
- Forschungserfahrung
- Master
- Datenbanken
4 Tage
PhD candidate (m/f/x) in the Research Training Group “Monoaminergic Neuronal Networks & Disease” – Mechanistic aspects of GPCR signaling
Ruhr-Universität Bochum —Bochum
- Teilzeit
- Forschungserfahrung
- Master
- Sprachkenntnisse werden vermittelt
Direkt bewerben
7 Tage
Site Activation Specialist - Germany
IQVIA —Bonn
- Vollzeit
- Bachelor

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Clinical Research Associate (CRA) (m/f/d), full-time

phenox GmbH
Bochum

Jetzt bewerben

Details zur Stelle

Festanstellung | Vollzeit

Leistungen

Firmenevents
Vermögenswirksame Leistungen

Qualifikationen

Nursing
Englisch
Forschungserfahrung
Microsoft Office

Vollständige Stellenbeschreibung

Remote, Bochum

Full-time

Permanent employee

YOUR JOB DUTIES

Take ownership of clinical study monitoring

You conduct site qualification, initiation, monitoring, and close-out visits — both on-site and remotely
You create clear, high-quality visit reports and keep everything on track within given timelines
You stay closely connected with your study sites, ensuring continuous support and follow-up
You ensure compliance with protocols and regulations (ISO 14155, GCP, EU MDR, FDA, etc.)
Most importantly, you safeguard the rights, safety, and well-being of study participants

Ensure data quality you can trust

You support submissions to Ethics Committees and competent authorities
You review and verify clinical data against source documentation, ensuring accuracy and completeness
You monitor informed consent processes and documentation
You ensure timely and accurate entry of data in EDC systems
You identify, document and follow-up on data queries, deviations, and open action items

Drive quality & compliance excellence

You keep Trial Master Files and site documentation audit-ready at all times
You identify and report protocol deviations, adverse events, and other critical findings in accordance with regulatory and internal requirements
You support audits and inspections with confidence
You assist with contracts, invoices, and other study related financial aspects
You follow — and help strengthen — SOPs and quality standards

Build strong site relationships

You act as a trusted partner to investigators and site staff
You train and guide sites on protocols, devices, and procedures
You create a positive, collaborative study environment

YOUR PROFILE

You have a degree in Life Sciences, Nursing, Biomedical Engineering, or a related field — or an equivalent combination of education and hands-on clinical research experience
You’ve gained 2–3+ years of experience in clinical research, including working as a CRA — ideally within medical device studies
You’re confident conducting site initiation, monitoring, and close-out visits in the DACH region (on-site and/or remote)
You’ve worked with Ethics Committees and Competent Authorities and understand their expectations
You have solid knowledge of GCP (ISO 14155) and EU MDR (2017/745); familiarity with FDA regulations (21 CFR) is a plus
You communicate fluently in English and German; any additional European language is a bonus
You’re open to travel (typically 30–70%) and enjoy being close to your study sites
You work independently, stay organized, and can manage multiple sites or studies at once
You have a strong attention to detail and a solution-oriented mindset
You’re proactive, collaborative, and enjoy working with different stakeholders
You manage your time effectively and stay on top of competing priorities
You’re comfortable working with EDC systems and MS Office tools

WE OFFER

Be part of an international and dynamic team where collaboration and a hands-on mentality drive daily work
A flexible working environment that supports a healthy work-life balance e.g. this role can be on-site in our Bochum office, hybrid or remote
Benefit from a comprehensive onboarding program to help you quickly feel at home and succeed in your role
Grow with us - we offer the possibility to evolve within the team and take on new responsibilities
A fair and motivating remuneration system that values your contribution
Attractive benefits such as a company pension scheme (bAV) and capital-forming benefits (VWL)
Celebrate successes together at regular company and team events
JobRad as a sustainable alternative for your commute to work and in your free time

About us

phenox GmbH is a specialized manufacturer of Class III medical devices for the treatment of neurovascular diseases, which are developed, manufactured and distributed. Our innovative technologies and solutions are used by neuroradiologists worldwide to treat strokes and aneurysms. We offer a growing portfolio of innovative treatment options - including long-established technologies.

Jetzt bewerben

Erweiterte Suche

clinical research Jobs in nordrhein westfalen

Clinical Research Associate (CRA) (m/f/d), full-time

Research Assistant / Clinical Reserach Coordinator (m/w/d)

Sr. Clinical Research Associate (Germany)

Clinical Research Associate (f/m/d) EMEA

Clinical Research Associate (m/w/d)

Senior Clinical Project Manager (m/w/d), full-time

Supervisor, Clinical Trial Materials

Research Position (PhD Position) (m/f/d)

Leiter*in (m/w/d) Koordinierungsstelle Klinische Studien / Clinical Research Support Unit

Biobank - Pre Clinical Research Assistant (m/w/d)

PhD Candidate (f/m/x) in Ophthalmic Epidemiology

Research Position (m/f/d) - Experimental Endocrinology and Tumor cell metabolism

Research Assistant / Clinical Research Coordinator (m/w/d)

Clinical Trial Materials Specialist I

Scientist in-vitro Pharmacology (m/f/d)

PhD candidate (m/f/x) in the Research Training Group “Monoaminergic Neuronal Networks & Disease” – Mechanistic aspects of GPCR signaling

Research Technician (m/f/d) – full time

PhD Candidate (m/f/d)

PhD candidate (m/f/x) in the Research Training Group “Monoaminergic Neuronal Networks & Disease” – Mechanistic aspects of GPCR signaling

Site Activation Specialist - Germany

Ich möchte aktuelle Job-E-Mails für Stellen als clinical research in nordrhein westfalen erhalten

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