Clinical Research Site Monitor I/II
vor 4 Wochen
Parexel FSP is seeking a dedicated Clinical Site Monitor I or II to work remotely. The primary responsibility of the Site Monitor is to uphold data integrity and data quality, ensuring adherence to ICH GCP and local regulations at the site level.
The monitoring activities will align with the Study Monitoring Plan (SMP) and will predominantly be conducted virtually, complementing any necessary on-site visits. The Site Monitor will work closely with the Site Manager to guarantee that the site complies with the study protocol and remains inspection-ready. Additionally, the role involves coordination with local institutions and investigators.
Required Experience- A minimum of 1 year of experience as a Clinical Research Associate with proven expertise in monitoring (both virtual and on-site).
- Experience in site activation processes.
- Background in feasibility assessments and site management.
- Experience overseeing Contract Research Organizations (CROs).
- Familiarity with submission processes (note: this role does not involve direct submissions).
- Proficient in utilizing systems such as Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF) (Florence).
- A Bachelor's degree or Registered Nurse (RN) in a relevant field, or an equivalent combination of education, training, and experience.
Parexel offers exceptional financial rewards, comprehensive training, and opportunities for professional development. Expect engaging challenges while maintaining a healthy work/life balance. We prioritize the well-being of our employees just as much as that of our patients.
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Clinical Research Site Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The Site Monitor plays a crucial role in ensuring the integrity and quality of data collected at clinical sites, adhering to ICH GCP and local regulations.Key ResponsibilitiesConduct monitoring activities in accordance with the Study Monitoring Plan (SMP),...
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Clinical Research Site Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The primary responsibility of the Site Monitor is to uphold data integrity and quality while ensuring adherence to ICH GCP and local regulations at the site level.The monitoring activities will be executed in accordance with the Study Monitoring Plan (SMP), with...
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Clinical Research Site Monitor I/II
vor 4 Wochen
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Clinical Research Site Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The successful candidate will play a crucial role in maintaining the integrity and quality of data collected during clinical trials.Key ResponsibilitiesEnsure compliance with ICH GCP guidelines and local regulations at the site level.Oversee data integrity and...
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Clinical Research Site Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The successful candidate will play a crucial role in ensuring the integrity and quality of clinical data while adhering to ICH GCP and local regulations at the site level.Key ResponsibilitiesConduct monitoring activities in accordance with the Study Monitoring...
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Clinical Research Site Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated and detail-oriented Clinical Site Monitor I or II to work remotely. The successful candidate will play a crucial role in ensuring the integrity and quality of clinical data while adhering to ICH GCP and local regulations at the site level.Key ResponsibilitiesConduct monitoring activities in accordance with...
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Clinical Research Monitor I/II
vor 4 Wochen
Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition OverviewPharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The primary focus of this role is to uphold the integrity and quality of data while ensuring adherence to ICH GCP and local regulations at the site level.Key ResponsibilitiesEnsure data integrity and quality throughout the clinical trial process.Monitor...
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Leipzig, Sachsen, Deutschland Pharmiweb VollzeitPosition Overview: Pharmiweb is seeking a dedicated Clinical Site Monitor I or II to work remotely. The primary role of the Site Monitor is to uphold the integrity and quality of data while ensuring adherence to ICH GCP and local regulations at the site level. Key Responsibilities: Ensure data accuracy and compliance with regulatory standards. Conduct site...
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