There are so many titles under the noc 33109. however, the duties which are given are only given for specific department.
I do perform those duties but under research department for various diseases.
so my question is, the duties given are those just example or has to be specific to the given department.
The list of duties I perform are given below, the duties which are in bold form are the one similar to the example of duties given under NOC 33109 but under different departments.
General
•Gain familiarity with protocols, GCP, and Centricity Research SOPs/WPs and processes.
•Ensure the safety and welfare of study participants.
•Greet visitors, ascertain the nature of business, and direct visitors to the employer or appropriate person.
•Assist the clinical team with paper and electronic filing and archiving.
•Support ordering and coordinating office and medical supplies as needed.
•Perform routine office functions like printing, scanning, faxing documents and receiving & distributing incoming regular and electronic mails and other materials .
•Supervise and train interns on procedures and the use of current software's.
•Instruct patient on clinical trial diagnostic test and record results.
•Assist with on-site quality control.
•Attend regularly scheduled site meetings, sponsor training or other meetings as required by the study.
•Perform various administrative duties like scheduling appointment's, answering telephone calls, greeting patients, handling mail, data entry, document tracking and filing & record keeping.
•Manage front desk supervision at sites that require this support and serve as backup to Administrative Assistant (in sites with this position).
Study-specific
•Create, maintain, update, and organize the Investigator Site File, ensuring compliance to GCP and Centricity SOPs/WPs and processes.
•Download and distribute files from portals (e.g., ethics, study-specific, etc.).
•Create and maintain the logs and documentation required per study.
•Enter and format electronically based medical reports and correspondence and prepare spreadsheets and documents for review.
•Document receipt, maintain inventory, organization, and documentation of Investigational Products and other study supplies.
•Assist in chart screening, database query reviews, and recruitment outreach efforts as needed.
•Instruct patients on various test procedures like Eye Exam, MRI and PET scans and record the results.
•Take patients' general medical, surgical and ophthalmic history for protocol specific visit.
•Assist the clinical team with scheduling and coordinating appointments for different study visits, reminding study participants of their appointments, and checking study participants in and out of their visits.
•Interview study patients to complete different referral forms like eye specialist visit and neuroimaging visit and case histories.
•Instruct patients and their families and other health care professionals with respect to clinical trial ophthalmic matters.
•Archive clinical research documents, track, and maintain all archived documents upon completion of a study.
•Set up and dismantle equipment.
•Prepare and maintain cleanliness of collection areas.
•Clean and maintain medical laboratory and medical laboratory equipment's.
•Collect, label, sort and prepare blood, tissue and other samples from study patients.
•Perform QC for completeness before data entry.
•Perform accurate, complete, and timely data entry of CRFs and query resolution.
•Support CRPs in addressing monitor findings, and follow-up.
•Provide technical support and training to study participants where required.
•Maintain confidential medical files and patient records.
I do perform those duties but under research department for various diseases.
so my question is, the duties given are those just example or has to be specific to the given department.
The list of duties I perform are given below, the duties which are in bold form are the one similar to the example of duties given under NOC 33109 but under different departments.
General
•Gain familiarity with protocols, GCP, and Centricity Research SOPs/WPs and processes.
•Ensure the safety and welfare of study participants.
•Greet visitors, ascertain the nature of business, and direct visitors to the employer or appropriate person.
•Assist the clinical team with paper and electronic filing and archiving.
•Support ordering and coordinating office and medical supplies as needed.
•Perform routine office functions like printing, scanning, faxing documents and receiving & distributing incoming regular and electronic mails and other materials .
•Supervise and train interns on procedures and the use of current software's.
•Instruct patient on clinical trial diagnostic test and record results.
•Assist with on-site quality control.
•Attend regularly scheduled site meetings, sponsor training or other meetings as required by the study.
•Perform various administrative duties like scheduling appointment's, answering telephone calls, greeting patients, handling mail, data entry, document tracking and filing & record keeping.
•Manage front desk supervision at sites that require this support and serve as backup to Administrative Assistant (in sites with this position).
Study-specific
•Create, maintain, update, and organize the Investigator Site File, ensuring compliance to GCP and Centricity SOPs/WPs and processes.
•Download and distribute files from portals (e.g., ethics, study-specific, etc.).
•Create and maintain the logs and documentation required per study.
•Enter and format electronically based medical reports and correspondence and prepare spreadsheets and documents for review.
•Document receipt, maintain inventory, organization, and documentation of Investigational Products and other study supplies.
•Assist in chart screening, database query reviews, and recruitment outreach efforts as needed.
•Instruct patients on various test procedures like Eye Exam, MRI and PET scans and record the results.
•Take patients' general medical, surgical and ophthalmic history for protocol specific visit.
•Assist the clinical team with scheduling and coordinating appointments for different study visits, reminding study participants of their appointments, and checking study participants in and out of their visits.
•Interview study patients to complete different referral forms like eye specialist visit and neuroimaging visit and case histories.
•Instruct patients and their families and other health care professionals with respect to clinical trial ophthalmic matters.
•Archive clinical research documents, track, and maintain all archived documents upon completion of a study.
•Set up and dismantle equipment.
•Prepare and maintain cleanliness of collection areas.
•Clean and maintain medical laboratory and medical laboratory equipment's.
•Collect, label, sort and prepare blood, tissue and other samples from study patients.
•Perform QC for completeness before data entry.
•Perform accurate, complete, and timely data entry of CRFs and query resolution.
•Support CRPs in addressing monitor findings, and follow-up.
•Provide technical support and training to study participants where required.
•Maintain confidential medical files and patient records.