What are the responsibilities and job description for the Medical Research Assistant position at Center for Advanced Research & Education?
Looking for a reliable self-starter with a positive attitude. Experience helpful but willing to train the right person. Ideal candidate should have education in the form of a Medical Assistant, Bachelor's Degree, or Master's Degree, or have had prior patient-related experience in a medical facility. They will be expected to perform a variety of clinical study activities to assist the Investigator in the conduct of a clinical study. Salary will be based on experience.
Responsibilities include but are not limited to:
Conduct the clinical study according to FDA regulations and guidelines.
Design and maintain organizational tools to conduct the study accurately and in compliance with GCP.
Ensure the safety and welfare of the study subjects.
Be knowledgeable of the Sponsor's protocol so that all study activities are completed correctly and completely.
Train other site personnel, and medical staff, on the specifics of implementing the protocol.
Screen potential study subjects according to the protocol's inclusion and exclusion criteria.
Obtain proper written informed consent from each study subject prior to participation in the study
Schedule study subjects' visits and during the study subject's visit perform defined activities of the study completely and accurately.
Report all adverse events to the Investigator.
Maintain adequate and accurate case histories for each study subject and record all observations in the source document and on the Case Report Form (CRF) or electronic Case Report Form (eCRF) during the study.
Complete the CRFs/eCRFs for the study accurately, completely, and in a timely fashion.
Assign study subject numbers and maintain accurate and complete records of the receipt, administration, and return of all clinical supplies. (Please refer to the Clinical Study Supplies SOP).
May assist the Regulatory Specialist/Clinical Trials Manager in maintaining required documentation in the study regulatory documentation file.
Maintain records of each study subjects' status in the study.
Communicate with the Sponsor regarding study activities as necessary.
Meet with the Sponsor's representatives to discuss the conduct of the study and review study data.
Job Type: Full-time
Pay: From $18.00 per hour
Schedule:
- Monday to Friday
Work Location: In person
Salary : $18
