26 Jobs für Clinical Trials Nurse
Stellenangebote Clinical Trials Nurse Jobs
Job vor 5 Tagen bei Jobleads gefunden
• Admont, Steiermark
Clinical Specialist AWC (m/f/) Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. [. .. ] hospital standards. Deliver handson training and inservices for nurses, wound care teams, surgeons, physicians, and allied staff on appropriate product selection and correct application. Provide onsite/ remote clinical support during trials, conversions, and golives to ensure safe and effective use. Build trusted relationships with key stakeholders: wound care nurses/ specialists, tissue viability teams, surgeons, diabetology/ vascular teams, procurement, pharmacy/ materials management, and hospital quality teams. Support the development and delivery of educational materials: protocols, dressing guides, competency checklists, and clinical FAQs. [. .. ] discussions; tailor communication to different audiences and levels of clinical expertise. Your Skills And Expertise Bachelors Degree or higher in Nursing, Public Health, Paramedic or related experience. Clinical background: Registered Nurse (RN) or equivalent (preferred) , or allied health/ scientific degree with strong wound care practice exposure. 3+ years in hospital clinical practice and/or Med Tech clinical specialist role; strong exposure to wound care (surgical wounds, pressure injuries, diabetic foot, venous leg ulcers) . Excellent training and facilitation skills; confident [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
Senior Manager Medical Affairs (mfd)
• München, Bayern
[. .. ] safety. We are currently searching a Senior Manager Medical Affairs (m/f/d) based in Munich. Summary The Global Manager Sr. Medical Affairs-HST (Manager MA HST) will provide both [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development and launch expertise as well as technical knowledge to assigned product line (s) of appropriate HST division. This person is responsible for aligning their team with HST Medical Affairs and other pertinent departments. Critical to this role is global and regional clinical knowledge of surgical medical devices environments of [. .. ] presentation and teaching skills. Self-motivated independent mulit-tasking team-oriented individual with exceptional follow through. -Industry experience preferred Degree in related clinical discipline or equivalent required Experienced and skilled Nurse/ Practitioner with significant surgical device background required. Active license or regional equivalent in good standing required. Minimum 5 years of related Surgical experience required. Experience with surgical tables lights table accessories and booms systems along with healthcare information technology implementation and training preferred. Knowledge of Baxter products and competitive products [. .. ] or financial information. To learn how you can protect yourself review our Recruitment Fraud Notice. Required Experience Senior Manager Key Skills Proofreading Adobe Acrobat FDA Regulations Manufacturing Controls Biotechnology Clinical Trials Research Development GLP c GMP Product Development Chemistry Writing Skills Employment Type: Full-Time Experience: years Vacancy: 1 #J-18808-Ljbffr 70789416 [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
GULP experts united
• Biberach, Baden- Württemberg
[. .. ] business partners Tailored further training opportunities and free language courses A wide range of employee benefits Your tasks n this challenging and exciting role, you will take [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on a medical-clinical assistant function and accompany clinical trials from preparation to implementation. You will look after test subjects, independently carry out medical procedures such as ECG recording and vital parameter measurements, collect and process human samples and ensure the monitoring and safety of study participants. With your high quality standards, you will actively contribute to the success of [. .. ] of medical material for the clinical trial, e. g. labeling of blood collection tubes Support with the possible emergency care of test subjects Your profile Completed medical training as a nurse, medical assistant, physicians assistant, emergency paramedic, with several years of relevant professional experience as a paramedic, emergency medical technician Confident handling of blood sampling techniques Careful, structured, effective and efficient way of working as well as strong organizational skills and high quality awareness Experienced with PC programs (e. g. MS [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
GULP experts united
Study Operation Support-Study Assistant (m/f/d)
• Biberach, Baden- Württemberg
[. .. ] g. electronically using suitable software Compliance with existing quality standards, legal or similar requirements (e. g. ICH-GCP) and internal standard operating procedures Your profile Completed medical training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a nurse, medical assistant, physician assistant or comparable practical relevant professional experience Experience in conducting clinical trials with healthy volunteers and good knowledge of GCP or willingness to acquire this knowledge with us Confident handling of blood sampling techniques Experienced with PC programs (e. g. MS Office, Teams) Fluent German, good written and spoken English skills Team player with strong communication skills and good time management The [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Rapid Trials
• Chemnitz
POSITION SUMMARY Rapid
Trials is hiring an experienced
Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. This part-time, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] freelance role is based in Chemnitz, Germany. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, and ensuring compliance with protocol, GDPR, and site SOPs. [. .. ] Germany (cross-border recognition if applicable) QUALIFICATIONS REQUIREMENTS Bachelors degree in life sciences, nursing, or healthcare (verified healthcare qualification required) Minimum 2 years experience as a CRC or clinical research nurse role Demonstrated prescreening/ recruitment experience, preferably in metabolic/ liver studies Proficiency with EMR (SAP experience preferred) , EDC, and CTMS systems. Prior experience with industry-sponsored trials is strongly desired Strong attention to detail, independent work ethic, and excellent communication skills Fluent in German and conversational in English; proof of [. .. ]
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 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. 70064962 [. .. ]
Job am 20.11.2025 bei Neuvoo.com gefunden
Tigermed
• 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 [. .. ]
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 [. .. ]
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 [...]
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. 70058366 [. .. ]
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 [...]
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. 70055606 [. .. ]
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 [...]
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. 70061095 [. .. ]
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 [. .. ]
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 [...]
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. 70063722 [. .. ]
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 [. .. ]
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 [. .. ]
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 [...]
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. 70064668 [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tigermed
• 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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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 [. .. ]
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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 26 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 (4 Jobs) und Niedersachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Nurse Jobs?
Clinical Trials Nurse Jobs gehören zum Berufsfeld Krankenpflege.
