Kompetenznetz Vorhofflimmern e.V. * Münster * Feste Anstellung * Vollzeit - Das Kompetenznetz Vorhofflimmern e.V. / Atrial Fibrillation NETwork (AFNET) sucht für die Leitung der Geschäftsstelle in Münster/Westfalen zum nächst ...

Developing project strategies for (complex) clinical research projects while assessing project risks and issues and providing solutions where applicable

Universitätsklinikum Köln (AöR) * Köln * Befristeter Vertrag * Teilzeit,Vollzeit - Arbeiten an der Uniklinik Köln und der Medizinischen Fakultät heißt die Zukunft mitzugestalten – die Zukunft der Medizin, der ...

Als internationales Auftragsforschungsinstitut (Clinical Research Organization - CRO) führen wir klinische Studien mit Medizinprodukten, In-vitro-Diagnostika (IVDs) und Arzneimitteln durch.

assist in the preparation of risk assessments and strategies for clinical testing and approval * monitor clinical trials and international regulatory approvals * completed Master's degree in computer ...

support the preparation of risk assessments and strategies for clinical testing and approval * create procedure descriptions and assist the application support team in the creation of training materials * ...

Sie sind erster Ansprechpartner für externe Partner (Clinical Research Associates und Clinical Research Organizations) bei der Durchführung von Studien im internationalen Umfeld

Verstärken Sie unser Team als CRA (Clinical Research Associate) / Klinischer Monitor (m/w/d) * Idealerweise eine Zusatzqualifikation als „Klinischer Monitor / Clinical Research Associate“

Besonders eng sind die Partnerschaften mit der Charité – Universitätsmedizin Berlin im gemeinsamen Experimental and Clinical Research Center (ECRC) und dem Berlin Institute of Health ...

This also encompasses the manufacture of materials for toxicological and early clinical studies. * Manufacture materials for toxicological studies and early clinical development according to international ...

Vertragsverhandlung mit der Clinical Research Organisations (CRO) für Nacharbeiten

ROXALL Medizin GmbH * Oststeinbek * Feste Anstellung * Vollzeit - ROXALL ist ein deutsches, international tätiges pharmazeutisches Unternehmen.

Besonders eng sind die Partnerschaften mit der Charité – Universitätsmedizin Berlin im gemeinsamen Experimental and Clinical Research Center (ECRC) und dem Berlin Institute of Health ...

We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing a range of cancers such as neuroendocrine cancers or bone metastases.

CRS Clinical Research Services Wuppertal GmbH

Minimum of 8 years of experience in the pharmaceutical industry and minimum of 5 years of experience in global regulatory affairs with emphasis on late stage drug development and marketing ...

The position is located within the Research and Clinical Bioanalytics (RCB) department of CSL Behring Innovation GmbH, Research. For our Research department we are looking for a

Bindeglied zwischen den Teammitgliedern und Office-basierten Lilly-Teams in der Medizin (Clinical Research Physicians, Clinical Research Scientists, Medical Affairs Professionals) und im Business (Brand Teams)

Sie unterstützen bei klinischer Nachweisführung vor und nach dem Inverkehrbringen von Medizinprodukten – Mit Clinical Evaluation, PMS und PMCF sind Sie vertraut.

FGK Clinical Research GmbH

This includes at least the development of study protocols, analysis plans and analysis execution and interpretation for clinical studies, non-interventional studies, RWE activities, external control arm ...

Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. ...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and ...

Clinical Research Associate - Home-based, Berlin and North Germany Area. Together, we help clients define anddevelop clinical programmes, minimise delays and execute high-quality, cost-efficient clinicalstudies. Experience of independent, on-site monitoring ...

Translation Research in Oncology (TRIO) is an academic clinical research organization that is dedicated to advancing translational cancer research by bringing forward innovative and targeted therapeutic concepts from the lab ...

PPD is currently recruiting for Clinical Research Associates (CRA) in Germany. Together, we help clients define anddevelop clinical programmes, minimise delays and execute high-quality, cost-efficient clinicalstudies. Independent, on-site monitoring experience ...

As part of this role, you will be responsible for overseeing studies, monitoring the progress of clinical trials at the site level or headquarters and ensure that they are conducted, ...

Our Clinical Delivery team is world class and as a Clinical Research Associate within our EMEA Clinical Delivery team you will have the opportunity to work within a structure that ...

The Clinical Research Manager (CRM,Ophthalmology) will function operationally as a member of a Project Team being responsible of coordinating and overseeing the Ophthalmology country and site management activities during study ...

Klinisches Monitoring bei aktuellen Studien (Phase 2-3).Einreichungsprozesse (Vorbereitung Ethikeinreichungen).Erfolgreich abgeschlossenes Naturwissenschaftliches Studium....

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and ...

Translation Research in Oncology (TRIO) is an academic clinical research organization that is dedicated to advancing translational cancer research by bringing forward innovative and targeted therapeutic concepts from the lab ...

In depth knowledge of clinical research regulations governing the conduct of the clinical trials and quality standards. Contribute to the continuous improvement of clinical operations through participation or lead in ...

The Senior Clinical Research Associate (sCRA) coordinates and performs site management and monitoring activities within the Site Management department of CATO SMS’ Clinical Trial Operations. We are currently recruiting for ...

Associated Keywords: Freelance, Contract Clinical Research Associate, CRA, Monitoring, Contract, Pharma, Full-time, Germany, Permanent, Senior CRA, Lead CRA, CRO, Clinical Research Organization, Pharmaceutical, Research, Clinical Trials. Freelance Clinical Research Associate, ...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and ...

As part of this role, you will be responsible for overseeing studies, monitoring the progress of clinical trials at the site level or headquarters and ensure that they are conducted, ...

In depth knowledge of clinical research regulations governing the conduct of the clinical trials and quality standards. Contribute to the continuous improvement of clinical operations through participation or lead in ...

Klinisches Monitoring bei aktuellen Studien (Phase 2-3).Einreichungsprozesse (Vorbereitung Ethikeinreichungen).Erfolgreich abgeschlossenes Naturwissenschaftliches Studium....

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and ...

The Senior Clinical Research Associate (sCRA) coordinates and performs site management and monitoring activities within the Site Management department of CATO SMS’ Clinical Trial Operations. We are currently recruiting for ...