Description Main purpose of the job: To screen, enroll, and follow up research study participants, conducting identify potential patients for research studies Enroll participants by educating them about the study consent according to SOPs Collaborate to meet study enrollment targets through dedication, solutions, teamwork maintain recruitment plans, including screening and enrolment logs daily Complete and file all relevant documentation minimum education and training: Certificate Enrolled Nursing (SANC registration) Demonstrable experience
Description Main purpose of the job: To screen, enroll, and follow up research study participants, conducting identify potential patients for research studies Enroll participants by educating them about the study consent according to SOPs Collaborate to meet study enrollment targets through dedication, solutions, teamwork maintain recruitment plans, including screening and enrolment logs daily Complete and file all relevant documentation minimum education and training: Certificate Enrolled Nursing (SANC registration) Demonstrable experience
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant reporting of delegated study activities, including enrolment logs, reimbursement logs and follow up reports and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
procurement, and stock in the clinic Lead the clinic team to ensure that all clinical trials are conducted in within the clinic Troubleshoot daily clinic operational issues in collaboration with the clinical operations comprehensive support of all operational aspects of clinical trials including overall delivery of protocol measure related initiatives in collaboration with the clinic operations manager Oversee maintenance and deployment/use related guidelines, etc.) in collaboration with the clinic operations manager Enforce organizational standard
procurement, and stock in the clinic Lead the clinic team to ensure that all clinical trials are conducted in within the clinic Troubleshoot daily clinic operational issues in collaboration with the clinical operations comprehensive support of all operational aspects of clinical trials including overall delivery of protocol measure related initiatives in collaboration with the clinic operations manager Oversee maintenance and deployment/use related guidelines, etc.) in collaboration with the clinic operations manager Enforce organizational standard