Clinical Trials Nurse Stellenangebote


+ Suchfilter (0 aktiv)

21 Jobs für Clinical Trials Nurse


Stellenangebote Clinical Trials Nurse Jobs


Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed

Contractor CRA-Tigermed Jyton-Germany (MJ000035)

• Munich Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70055606 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Stuttgart Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70064668 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Leipzig Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70063722 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Hamburg Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70061095 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Düsseldorf Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70058366 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Essen Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70064962 [. .. ]

▶ Zur Stellenanzeige
Button Jobabo Nichts verpassen: Jobs per eMail
► Speichern Sie jetzt Ihre Jobsuche!

Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Dortmund Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70065179 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Frankfurt Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70059668 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Berlin Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70061230 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) • Cologne Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70063472 [. .. ]

▶ Zur Stellenanzeige
Job am 20.11.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany (MJ000035) Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70056983 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Frankfurt Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65911382 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed

Contractor CRA-Tigermed Jyton-Germany

• Cologne Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65924645 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Essen Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65912943 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65923487 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Hamburg Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65927535 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Berlin Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65916018 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Dortmund Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65927277 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Düsseldorf Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65906870 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Munich Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65910884 [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden Tigermed Contractor CRA-Tigermed Jyton-Germany • Stuttgart Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Tigermed Jyton or sponsor Standard Operating Procedures (SOPs) , International Conference on Harmonization Good Clinical Practice standard (GCP) ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. [. .. ] Study Tools and system Update and maintain Study tools/ systems in a timely manner. Minimum Qualifications 1. Academic/ Major: Bachelor degree in biomedical/ medical science or equivalent (e. g. medical, Nurse, Pharmacology) . 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65935218 [. .. ]

▶ Zur Stellenanzeige
Jobs



Häufig gestellte Fragen

Wieviel verdient man als Clinical Trials Nurse pro Jahr?

Als Clinical Trials Nurse verdient man zwischen EUR 40.000,- bis EUR 65.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Trials Nurse Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 21 offene Stellenanzeigen für Clinical Trials Nurse Jobs.


In welchen Bundesländern werden die meisten Clinical Trials Nurse Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Trials Nurse Jobs werden derzeit in Nordrhein-Westfalen (6 Jobs), Baden-Württemberg (2 Jobs) und Niedersachsen (2 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Trials Nurse Jobs?

Clinical Trials Nurse Jobs gehören zum Berufsfeld Krankenpflege.


Jobs per Email


Verpassen Sie keine Jobs!
Wir informieren Sie kostenfrei über neue Jobangebote!


Datenschutzklärung lesen


Dauer: 0.0437 s., Vers. V.2025-d-2008-Ind-141