20 beste Stellen als clinical data in deutschland – aktuell auf Personalsuche

Clinical Site Associate
ICON Plc —Frankfurt am Main
- Vollzeit
- Forschungserfahrung
- Microsoft Office
- Bachelor
13 Tage
Clinical Research Coordinator
Parexel —Berlin
- Wochenendarbeit möglich
- Windows
- PC-Kenntnisse
Medical Reviewer for Clinical Data
Excelya —Freiburg
- Vollzeit
- Hybrides Arbeiten
- Doktorat
- Master
Direkt bewerben
13 Tage
Clinical Research Associate (CRA) (m/f/d), full-time
phenox GmbH —Bochum
- Vollzeit
- Hybrides Arbeiten
- Nursing
- Englisch
- Forschungserfahrung
Clinical Trial Manager (f/m/d)
Nia Health GmbH —Berlin-Kreuzberg
- Teilzeit
- Medizin
- Doktorat
- Krankenhaus
- Weiterbildungsprogramme
Direkt bewerben
Clinical Trial Manager
Ambu —Augsburg
- Vollzeit
- Hybrides Arbeiten
13 Tage
Talent wanted (all)
mediaire GmbH —Berlin
- Vollzeit
Direkt bewerben
Senior Clinical Project Manager (m/w/d), full-time
phenox GmbH —Bochum
- Vollzeit
- Hybrides Arbeiten
- Nursing
- Forschungserfahrung
- Master
Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Lübeck
- Vollzeit
- Microsoft Office
- Bachelor
- Organisationstalent
Direkt bewerben
Quality Assurance Lead (all genders)
Avelios Medical GmbH —München
- Vollzeit
- Produktmanagement
- Führungserfahrung
- Flexible Arbeitszeiten
Clinical Research Associate (m/w/d)
MSD —Schwabenheim
- Vollzeit
- Englisch
- Microsoft Office
- Mit Reiseanteil
9 Tage
Clinical Research Associate / Klinischer Monitor (m/w/d)
IGES GmbH —Berlin
- Online-Bewerbung
- Englisch
- Analysefähigkeit
- Organisationstalent
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Direkt bewerben
Clinical Data Repository Projektmanager (w/m/d)
AGAPLESION Management- und Beratungsgesellschaft gGmbH —Frankfurt am Main
- Teilzeit
- Informatik
- Projektmanagement
- Gleitzeit
- Weiterbildungsprogramme
Direkt bewerben
13 Tage
Clinical Trial Transparency Associate
ICON Plc —Frankfurt am Main
- Vollzeit
- Microsoft Excel
- Projektmanagement
- Bachelor
Clinical Research Associate II/III - Germany
Optimapharm d.o.o. —Berlin
- 50.000 € – 60.000 € pro Jahr
- Vollzeit
- Homeoffice
- Nursing
- Forschungserfahrung
- Master
- Flexible Arbeitszeiten
- Empfehlungsprogramm
Clinical Site Coordinator / Studienkoordinator
Milestone One —Kassel
- Teilzeit
Direkt bewerben
Medical Consultant (all genders)
Avelios Medical GmbH —München
- Vollzeit
Solutions Consultant
Certara —Home Office
- Vollzeit
- Homeoffice
- Bachelor
2 Tage
Systems Navigator (SN) - Bavaria, Germany
Patriot Enterprises LLC —Bayern
- Vollzeit
- Militär
- Microsoft Office
- Bachelor
Direkt bewerben
7 Tage
Clinical Research Associate (CRA) (m/w/d) – Zelltherapie (Außendienst)
AstraZeneca —Hamburg
- Englisch
- Mit Reiseanteil
- Kommunikationsfähigkeit

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Clinical Site Associate

ICON Plc -
Frankfurt am Main

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 13 Tagen

Qualifikationen

Forschungserfahrung
Microsoft Office
Bachelor
Dateneingabe

Vollständige Stellenbeschreibung

Clinical Site Associate Germany

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.

What You Will Do:

You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Supporting site activation activities, including the collection, review, and tracking of essential documents and approvals.
Maintaining up-to-date site information and status in clinical trial management systems and trackers.
Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions.
Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness.
Collaborating with internal stakeholders to support timely site payment processing and issue resolution.
Contributing to process improvement initiatives and sharing best practices to enhance site support efficiency.

Your Profile:

You will bring relevant scientific operations experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in life sciences, healthcare or a related field, or equivalent experience.
Initial experience in clinical research, administration, or a similar regulated environment is preferred.
Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines.
High attention to detail and accuracy in documentation and data entry.
Effective written and verbal communication skills, with a customer-focused approach to site support.
Proficiency with MS Office and comfort working with electronic systems and databases.
Ability to work collaboratively in a team environment and adapt to changing priorities.
Willingness to travel as required (approximately 10%)
Excellent communication skills in German and English

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Jetzt bewerben

Erweiterte Suche

clinical data Jobs in deutschland

Clinical Site Associate

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Medical Reviewer for Clinical Data

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

Clinical Trial Manager (f/m/d)

Clinical Trial Manager

Talent wanted (all)

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

Clinical Research Coordinator I

Quality Assurance Lead (all genders)

Clinical Research Associate (m/w/d)

Clinical Research Associate / Klinischer Monitor (m/w/d)

Clinical Data Repository Projektmanager (w/m/d)

Clinical Trial Transparency Associate

Clinical Research Associate II/III - Germany

Clinical Site Coordinator / Studienkoordinator

Medical Consultant (all genders)

Solutions Consultant

Systems Navigator (SN) - Bavaria, Germany

Clinical Research Associate (CRA) (m/w/d) – Zelltherapie (Außendienst)

Ich möchte aktuelle Job-E-Mails für Stellen als clinical data in deutschland erhalten

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