33 Jobs für Clinical Study Coordinator
Stellenangebote Clinical Study Coordinator Jobs
Job vor 8 Tagen bei Jobleads gefunden
• Lüchow, Niedersachsen
[. .. ] 2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role Relevant prior Pharma/ Biotech Sponsor employment or experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical study coordinator preferred Experience in the drug discovery/ development process. Competencies Knowledge and understanding of clinical research processes, regulations and methodology Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management Working knowledge of ICH/ GCP Guidelines and applicable local laws and regulations (that govern clinical [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Clinical Study Coordinator Oncology Trials
• Wiener Neustadt, Niederösterreich
Med Austron Gmb H in Wiener Neustadt sucht eine/n
Clinical Study Specialist zur aktiven Mitgestaltung klinischer Studien im Behandlungsspektrum der Protonen- und Kohlenstoffionentherapie. Sie koordinieren Patientenregister und Studien, unterstützen Planung, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Durchführung und Nachverfolgung von Forschungsprojekten und arbeiten eng mit Radioonkologie, Patientenadministration sowie weiteren Schnittstellen zusammen. #J-18808-Ljbffr 02049237 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Clinical Research Associate (m/w/d) Region: Stuttgart, Heilbronn, Heidelberg
• München, Bayern
[. .. ] 2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role. Relevant prior Pharma/ Biotech Sponsor employment or experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a clinical study coordinator preferred. Experience in the drug discovery/ development process. Competencies Knowledge and understanding of clinical research processes, regulations and methodology. Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management. Working knowledge of ICH/ GCP Guidelines and applicable local laws and regulations to ensure compliance [. .. ]
Job vor 11 Tagen bei StepStone gefunden
Carl von Ossietzky Universität Oldenburg
Forschungs- und Studienkoordination in der Kinder- und Jugendpsychiatrie und psychotherapie
• Oldenburg
Teilzeit Homeoffice möglich Abgeschlossenes Studium Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Public Health, Medizinmanagement, Wirtschaftswissenschaften, Gesundheitswissenschaften oder einer vergleichbaren Fachrichtung oder Hochschulabschluss und mehrjährige berufliche Erfahrung im Aufgabenbereich oder abgeschlossene Berufsausbildung im medizinischen Bereich sowie (möglichst) eine abgeschlossene [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Prüfung zumzur Studienassistentin (Study Nurse) Ausgeprägte Kommunikations- und Organisationsfähigkeiten sowie ein hohes Maß an Selbstständigkeit und Zuverlässigkeit Strukturierte und sorgfältige Arbeitsweise Sehr gute Englischkenntnisse in Wort und Schrift Fließende Deutschkenntnisse in Wort und Schrift Von Vorteil sind Gute EDV Kenntnisse, insbesondere in den Bereichen Textverarbeitung, Tabellenkalkulation (z. B. Excel) und grafische Darstellung von Daten Erfahrungen im wissenschaftlichen Arbeiten und/oder Projektmanagement Erfahrungen im Umgang mit Forschungsdatenbanken oder Studienregistern Weiterbildungen: Good-Clinical-Practice-(GCP) - Zertifikat, Kurs zur Studienkoordination, Weiterbildung Clinical Research Associate (CRA) , Weiterbildung Clinical Research Coordinator (CRC) , Projektmanagement (z. B. PRINCE2, PMP, Scrum) , Drittmittelmanagement, Forschungsdatenmanagement, Medizinische Statistik, Datenschutz im Gesundheitswesen, Forschungsrecht und Ethik Wir bieten Strukturierte Einarbeitung, intensive Betreuung und eine kollegiale Arbeitsatmosphäre, die Ihre fachliche und persönliche Weiterentwicklung unterstützt Mitarbeit in innovativen, interdisziplinären Forschungsprojekten im Bereich der klinischen Kinderpsychologie und psychiatrie Möglichkeit, eigene [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
• Dortmund, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Munich, BY Muenchen
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Hamburg, HH
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Frankfurt
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Berlin, BE
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Stuttgart, BW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Essen, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Hessen
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Saxony Leipzig
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Baden- Württemberg
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Bavaria Munich
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] to the Company forums, boards and/or discussions. Assist sites with enrollment barriers by reinforcing protocol specific site recruitment plans. Support assigned studies from a regional and cultural perspective support study teams with quality related visits as needed. Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites. Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities. Travel including overnight stays, possibly global, up to 50. Qualifications: Terminal Scientific [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
Job vor 10 Tagen bei JobMESH gefunden
Carl von Ossietzky Universität Oldenburg
• Niedersachsen 26129 Oldenburg
Abgeschlossenes Studium Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Public Health, Medizinmanagement, Wirtschaftswissenschaften, Gesundheitswissenschaften oder einer vergleichbaren Fachrichtung oder Hochschulabschluss und mehrjährige berufliche Erfahrung im Aufgabenbereich oder abgeschlossene Berufsausbildung im medizinischen Bereich sowie (möglichst) eine abgeschlossene [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Prüfung zumzur Studienassistentin (Study Nurse) Ausgeprägte Kommunikations- und Organisationsfähigkeiten sowie ein hohes Maß an Selbstständigkeit und Zuverlässigkeit Strukturierte und sorgfältige Arbeitsweise Sehr gute Englischkenntnisse in Wort und Schrift Fließende Deutschkenntnisse in Wort und Schrift Von Vorteil sind Gute EDV-Kenntnisse, insbesondere in den Bereichen Textverarbeitung, Tabellenkalkulation (z. B. Excel) und grafische Darstellung von Daten Erfahrungen im wissenschaftlichen Arbeiten und/oder Projektmanagement Erfahrungen im Umgang mit Forschungsdatenbanken oder Studienregistern Weiterbildungen: Good-Clinical-Practice-(GCP) - Zertifikat, Kurs zur Studienkoordination, Weiterbildung Clinical Research Associate (CRA) , Weiterbildung Clinical Research Coordinator (CRC) , Projektmanagement (z. B. PRINCE2, PMP, Scrum) , Drittmittelmanagement, Forschungsdatenmanagement, Medizinische Statistik, Datenschutz im Gesundheitswesen, Forschungsrecht und Ethik Wir bieten Strukturierte Einarbeitung, intensive Betreuung und eine kollegiale Arbeitsatmosphäre, die die fachliche und persönliche Weiterentwicklung unterstützt Mitarbeit in innovativen, interdisziplinären Forschungsprojekten im Bereich der klinischen Kinderpsychologie und -psychiatrie Möglichkeit, eigene [. .. ]
Neu Job vor 2 Std. bei Stellen-Online.de gefunden
Medpace
Clinical Project Coordinator-Vollzeit
• München, 80331 Muenchen
Job Summary Due to continuous business growth and a strong
study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the companys success. Responsibilities Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; [. .. ]
Neu Job vor 2 Std. bei Stellen-Online.de gefunden
UCB Group
• Mettmann, 40822
Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing Environment Business
Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Reporting team, based in any of our Brussels (Belgium) , Monheim (Germany) , Raleigh (USA) , or Slough (UK) offices. About the role You will help clinical programming teams move to and work confidently within UCBs modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs. Who youll work with You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business [. .. ]
Neu Job vor 2 Std. bei Stellen-Online.de gefunden
Medpace
Regulatory Submissions Coordinator-Vollzeit
• München, 80331 Muenchen
Job Summary Our
clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions
Coordinator to join our Clinical Operations team in Munich. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. [. .. ] to collect all essential documents required before the site starts to enroll patients to participate in the clinical trial; Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration; Ensure submissions comply with applicable regulations and guidance documents; Advise on changing country regulations and compliance requirements; and Track submissions and ensure timely filing of documents. Qualifications Bachelor s degree (preferably in a Life Sciences field) ; Interest in drug development and [. .. ]
Job vor 10 Tagen bei Stellen-Online.de gefunden
Carl von Ossietzky Universität Oldenburg
Forschungs- und Studienkoordination in der Kinder- und Jugendpsychiatrie und -psychotherapie-Teilzeit
• Oldenburg, 26129, 26122
Teilzeit Abgeschlossenes Studium Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Public Health, Medizinmanagement, Wirtschaftswissenschaften, Gesundheitswissenschaften oder einer vergleichbaren Fachrichtung oder Hochschulabschluss und mehrjährige berufliche Erfahrung im Aufgabenbereich oder abgeschlossene Berufsausbildung im medizinischen Bereich sowie (möglichst) eine abgeschlossene [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Prüfung zumzur Studienassistentin (Study Nurse) Ausgeprägte Kommunikations- und Organisationsfähigkeiten sowie ein hohes Maß an Selbstständigkeit und Zuverlässigkeit Strukturierte und sorgfältige Arbeitsweise Sehr gute Englischkenntnisse in Wort und Schrift Fließende Deutschkenntnisse in Wort und Schrift Von Vorteil sind Gute EDV-Kenntnisse, insbesondere in den Bereichen Textverarbeitung, Tabellenkalkulation (z. B. Excel) und grafische Darstellung von Daten Erfahrungen im wissenschaftlichen Arbeiten und/oder Projektmanagement Erfahrungen im Umgang mit Forschungsdatenbanken oder Studienregistern Weiterbildungen: Good-Clinical-Practice-(GCP) - Zertifikat, Kurs zur Studienkoordination, Weiterbildung Clinical Research Associate (CRA) , Weiterbildung Clinical Research Coordinator (CRC) , Projektmanagement (z. B. PRINCE2, PMP, Scrum) , Drittmittelmanagement, Forschungsdatenmanagement, Medizinische Statistik, Datenschutz im Gesundheitswesen, Forschungsrecht und Ethik Wir bieten Strukturierte Einarbeitung, intensive Betreuung und eine kollegiale Arbeitsatmosphäre, die die fachliche und persönliche Weiterentwicklung unterstützt Mitarbeit in innovativen, interdisziplinären Forschungsprojekten im Bereich der klinischen Kinderpsychologie und -psychiatrie Möglichkeit, eigene [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Medpace
Clinical Safety Coordinator-Pharmacovigilance/ Drug Safety-Vollzeit
• München, 80331
Job Summary At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. As such, we are searching for motivated individuals to join our
Clinical Safety team in London. Working [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines. If you want [. .. ] oversight and compliance reports) Additional Responsibilities Develop presentation material and present during face-to-face Sponsor meetings (i. e. , Kick-off Meetings, Investigator Meetings) Coordinate final medical review of study report narratives and submission to Medical Writers Develop drafts of adjudication material (i. e. , charter, reporting materials) Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor Train new Clinical Safety Coordinators on safety reporting responsibilities Coordinate safety responsibilities for aggregate reporting purposes (e. g. [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Medpace
Clinical Trial Site Relationship Coordinator-Vollzeit
• München, 80331
Job Summary Our
clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship
Coordinator to join our vibrant Clinical Operations team in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Germany, Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities across the DACH region. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. If you want an exciting career [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Associate (Germany)
• Berlin
Junior
Clinical Research Associate (Germany) Role Summary The role supports the organization and execution of clinical studies in Germany. It involves working with internal teams and external partners to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure that studies run smoothly, in accordance with timelines, quality standards, and applicable regulations. Key Responsibilities Support the coordination and day-to-day follow-up of clinical studies. Work closely with clinical sites and internal teams throughout the different stages of a study. Help prepare and activate study sites and support patient recruitment activities. Follow up on study progress, timelines, documentation, and overall site performance. Support the review of study data and documentation to ensure quality and completeness. Help identify and resolve issues that may arise during the study. Support compliance with study [. .. ] and fast-paced environment. Required Qualifications Relevant background in life sciences, healthcare, nursing, engineering, or a related field. A first relevant experience in clinical research (CTA, Study start-up, Study Coordinator, . . . ) Good knowledge of clinical trial processes and GCP principles. Fluency in German and English. Good organizational, communication, and problem-solving skills. Ability to manage priorities and work independently while collaborating with a wider team. Good knowledge of MS Office and experience with relevant clinical systems. Willingness to [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Team Leader (Player/ Manager) Clinical Development Liaison (CDL) Neuromuscular Diseases-Germany
Führungs-/ Leitungspositionen
[. .. ] resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Leader (Player/ Manager) Clinical Development Liaison (CDL) Neuromuscular Diseases Business Unit : Field Operations Reports to: Program Director, Medical, Amplity Location: Germany Territory: Germany and some other countries in Europe Role Type: Individual Contributor with Leadership Responsibilities (Player-Coach) About the Role Amplity is partnering with an innovative global biopharmaceutical company dedicated to advancing [. .. ] field-based role combining scientific leadership, stakeholder engagement, and operational support for clinical trial execution. As a Clinical Development Liaison, you will serve as a key scientific partner to investigators, study sites, and internal stakeholders, supporting study start-up, patient identification, enrollment strategies, and study conduct. In addition, as a Player-Coach, you will provide mentorship, guidance, and leadership to fellow CDL team members, helping drive consistency, best practices, and operational excellence across the region. This role offers the opportunity to [. .. ] regional experts, they will gain insight into treatment patterns and trends that will be shared internally to shape strategy. The role is also the field-based leader and key contributor/ coordinator to the overall remit of the clients Medical Affairs organisation for the Amplity Medical team. This position is responsible for leading and coordinating operational requirements of the Amplity team to support the clients Medical Affairs business. The specific deliverables being managed can vary and is defined in the contract Amplity [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Study Coordinator pro Jahr?
Als Clinical Study Coordinator verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Study Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 33 offene Stellenanzeigen für Clinical Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Study Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Coordinator Stellenangebote:
- Medpace (4 Jobs)
- UCB Group (1 Job)
- Herman Medical Staffing GmbH (1 Job)
In welchen Bundesländern werden die meisten Clinical Study Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Coordinator Jobs werden derzeit in Niedersachsen (6 Jobs), Bayern (6 Jobs) und Baden-Württemberg (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?
Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.
