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Clinical research associate Jobs in Erzhausen

Zuletzt aktualisiert: vor 3 Tagen
Sr. Clinical Research Associate

Sr. Clinical Research Associate

AvaniaHesse, DE
Vollzeit
Avania is hiring Senior Clinical Research Associates (Sr CRAs) .Avania’s ClinOps Team establishes, maintains and supports clinical trials. as a key member of the team, our Sr CRA pe...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
Quality Assurance Associate

Quality Assurance Associate

MarkenKelsterbach, Germany
Quality Assurance Associate (m / f / d).To mainly provide support to the CAPA System, Trainings and Vendor qualification process and records review. Main Duties and Responsibilities : .Maintain the cultur...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Research Liaison Officer (m / w / d)

Research Liaison Officer (m / w / d)

GSI Helmholtzzentrum für Schwerionenforschung mbHDarmstadt, Deutschland
Zur Verstärkung des Projektteams suchen wir zum 01.Research Liaison Officer (m / w / d) Kennziffer : 25.Die Tätigkeit umfasst : Koordination und Moderation von Co-Creation-Workshops : Initiierung, Durc...Mehr anzeigenZuletzt aktualisiert: vor 25 Tagen
Senior Research Scientist Molecular Biology

Senior Research Scientist Molecular Biology

AB EnzymesDarmstadt, DE
R&D and business environment, working with cutting edge technologies involved in a broad portfolio of diverse projects.The role requires a strong background in Molecular Biology and Fungal genetics...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

Edwards LifesciencesGermany, Hessen, Remote
Homeoffice
Vollzeit
Innovation starts from the heart.At Edwards, we put patients first.We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical inn...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
BTA (m / w / d)

BTA (m / w / d)

GULP Information Services GmbHDarmstadt, Hessen, Germany
Für einen Geschäftspartner aus der .Randstad professional solutions derzeit einen .Ein sicheres und faires Einkommen und gute Sozialleistungen sind Ihnen genauso wichtig wie eine verantwortungsvoll...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
Research Associate (m / f / d), Pharmacometrics

Research Associate (m / f / d), Pharmacometrics

Paul-Ehrlich-InstitutLangen, Germany
Research Associate (m / f / d), Pharmacometrics.Section "Data Science and Methods" as soon as possible.About the Paul-Ehrlich-Institut. We are a senior federal authority responsible for vaccines and bio...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Associate Director Clinical Data Manager (all genders)

Associate Director Clinical Data Manager (all genders)

Merck KGaA, Darmstadt, GermanyDarmstadt, Germany
A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team. As an Associate Director Clinical Data Manage...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Research Coordinator, Medical (m / f / d)

Research Coordinator, Medical (m / f / d)

International SOSNeu-Isenburg, DE, 63263
As a Research Coordinator, Medical (m / f / d) you will be responsible for the research, case management and submission of requests delivered through the European Union Agency for Asylum (EUAA) contrac...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Support Quality Associate

Support Quality Associate

AutodeskDarmstadt, Germany
Homeoffice
Vollzeit
We are looking for an accountable, impactful, and innovative Support Quality Associate (SQA) to expand our world-renowned Customer Support Team. As an SQA, reporting to the Quality Manager, you will...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Engineer or Physicist for supervision of superconducting magnet production and the testing Reference : 25.23-6352

Engineer or Physicist for supervision of superconducting magnet production and the testing Reference : 25.23-6352

GSI Helmholtzzentrum für Schwerionenforschung GmbHDarmstadt
The GSI Helmholtz Centre for Heavy Ion Research (Helmholtzzentrum für Schwerionenforschung), a member of the Helmholtz Association of German Research Centres, is one of the largest investigation ce...Mehr anzeigenZuletzt aktualisiert: vor 4 Tagen
  • Gesponsert
Quality Strategy Lead Development (all genders) - Inklusiver Job 🦼 🦻 🦯

Quality Strategy Lead Development (all genders) - Inklusiver Job 🦼 🦻 🦯

MerckDarmstadt, Hessen, DE
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives wi...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
BTA (m / f / d)

BTA (m / f / d)

GULP – experts unitedDarmstadt
Randstad professional solutions is currently looking for a.A secure and fair income and good social benefits are just as important to you as a responsible job and a long-term perspective as a.Then ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Warehouse Associate / Lagerlogistik Mitarbeiter

Warehouse Associate / Lagerlogistik Mitarbeiter

Marken Time Critical Express GmbHKelsterbach, Hessen, Germany
Quick Apply
Der Warehouse Associate ist für die Bestandsverwaltung und die gesamte Lagerhaltung in der Marken-Niederlassung verantwortlich. Er arbeitet mit allen von Marken betriebenen Filialen und deren Vertre...Mehr anzeigenZuletzt aktualisiert: vor 19 Tagen
  • Gesponsert
Clinical Education and Training Specialist (f / m / d)

Clinical Education and Training Specialist (f / m / d)

SprintRay Europe GmbHWeiterstadt bei Darmstadt, Germany
SprintRay is a forward-thinking, nimble company on ajourney to provide digital dentistry solutions to our customers.Since 2014 we have produced products that are advanced,user-friendly, and offer a...Mehr anzeigenZuletzt aktualisiert: vor 19 Tagen
  • Gesponsert
Post-doctoral researcher - Functional Genomics in AML

Post-doctoral researcher - Functional Genomics in AML

Universitätsklinikum FrankfurtDreieich
Knowledge becomes health" - we are filling this motto with life every day, developing new ideas and improv-ing old-established knowledge. The University Hospital Frankfurt has existed since 1914.Ou...Mehr anzeigenZuletzt aktualisiert: vor 8 Tagen
Research Associate for Software Analysis

Research Associate for Software Analysis

Fraunhofer-GesellschaftDarmstadt
To strengthen the Testlab Mobile Security department, we are looking for motivated employees with sound knowledge in the field of IT security. Tasks include deep static software analysis using newly...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Associate Finance 1+

Associate Finance 1+

Schollmeyer&SteidlHessen
Diese weltweit agierende Kanzlei sucht Verstärkung für den florierenden Finance-Bereich.In den letzten Jahren erlebte das Team ein gesundes Wachstum und soll nun auf Associate Ebene weiter verstärk...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Site Coordinator

Site Coordinator

Cummins Inc.Gross-Gerau, DEU
In this role, you will make an impact in the following ways : .Assist with Health, Safety, and Environment (HSE) related tasks, ensuring compliance with established guidelines and promoting a safe wo...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Sr. Clinical Research Associate

Sr. Clinical Research Associate

AvaniaHesse, DE
Vor 9 Tagen
Anstellungsart
  • Vollzeit
Stellenbeschreibung

Avania is hiring Senior Clinical Research Associates (Sr CRAs)

Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the trials, verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable (from source documents). Partnering closely with our Trial sites, Avania's Sr CRA ensures that the conduct of the trial follows approved protocols / amendment(s), with ISO14155 or ICH-GCP, and with applicable regulatory requirements.

Our Senior CRA role includes the following key activities -

  • Interact with and guide study investigators and study coordinators in conducting clinical trials in accordance with study protocols. Member of a site Start-up Team for assigned projects.
  • Monitor site’s completion of action items between visits and help prepare for audits and inspections; conduct and write accurate visit reports in accordance with SOPs and GCP (SQV, SIV, IMV, COV)
  • Ensure data entered on the CRFs is timely, accurate and verified. Collaborate with analytical services to obtain clean database, resolve queries and conduct or participate in data reviews (both internally and with sponsor), identifying and communicating trends or erroneous data.
  • Participate in internal TMF reviews, as needed.
  • Develop and maintain trackers, such as visit reports trackers, site trackers, recruitment and enrollment trackers.
  • Review and write informed consent forms. Review of protocols, investigator brochures on compliance with applicable regulations and CRFs in development. Prepare clinical trial agreements and present to site and study sponsor.
  • Review regulatory compliance for study documents and protocols.
  • May act as a Clinical Lead, overseeing clinical trial activities at investigational sites (will require travel to investigational sites).

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply. With our continued growth we are hiring talent to join us on our journey and grow with us.

Sr CRAs require skills in planning and preparation; sourcing and collecting information; prioritizing tasks and actions; and displaying a proactive attitude to assist in project planning and study execution.

We seek -

  • B.A. / B.S. or equivalent experience in a (para)medical, scientific or health related discipline or related work experience.
  • Minimum 3-7 years of relevant CRA work experience, with extensive cardiology Class III device monitoring experience.
  • Tracker and Start-up experience (with good spreadsheet or similar skills)
  • Ability to understand basic and complex medical details.
  • GCP-ICH-E6, FDA regulations and ISO 14155, 13485 and 9001 knowledge where applicable; knowledge of / ability to learn regulations and guidelines on medical devices and clinical trials.
  • Ability to travel up to 75% domestically and internationally.
  • Experience as a Clinical Lead helpful
  • Strong communicator with excellent presentation skills; able to build rapport with site personnel
  • We offer -

  • The opportunity to work in an innovative, fast-growing and rewarding industry
  • A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties
  • Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities
  • Competitive compensation and benefits package (details shared during the interview process)
  • Some roles offer the opportunities for travel
  • Ask us about our hybrid and fully remote work opportunities
  • We look forward to receiving your application!

    When you need to advance your career, it takes Avania!

    LI-DNI