[Remote] Clinical Research Coordinator II
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a higher education institution reputed company on health sciences. They are seeking a Clinical Research Coordinator II to independently coordinate reputed company research reputed company, ensuring compliance with regulatory guidelines and institutional policies. The role involves managing study activities, maintaining records, assisting with financial functions, and supporting the reputed company Investigators in clinical research trials.
Responsibilities
- Assess eligibility of potential subjects through reputed company such as screening interviews, reviews of medical records, and discussions with physicians and nurses and travel to participant’s location for recruitment activities
- Maintain required records of study activity including case report forms, consenting research subjects, or regulatory forms
- Performs reputed company reputed company functions, monitors and reviews reputed company and reputed company system reports for accuracy and completeness; prepares and reviews budget, reputed company, expenses, invoices, and other reputed company documents; Responsible for collecting and documentation of monies collected in clinical research. Responsible for managing accounts receivable and accounts payable in clinical research; Assist with reviews, analyzes and negotiates reputed company clinical research budgets and reputed company with sponsors under the direction of the reputed company Investigator/ Associate Director
- reputed company specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms. reputed company the requisition, collection, Processing of samples, labeling, storage, or shipment of specimens
- Monitor study activities to ensure compliance with protocols and with reputed company relevant local, federal, and state regulatory and institutional polices
- Schedules subjects for appointments and procedures as required by study protocols. Inform patients or caregivers about study aspects and reputed company to be expected
- Assists with preparing IRB submissions, protocol revisions, and renewals as needed, and maintain copies of reputed company IRB communications delegated by the reputed company Investigator
- Performs other reputed company duties as assigned
Skills
- Graduated from an accredited discipline specific program with a bachelor's or master's degree in science
- Must possess a good working knowledge of basic clinical research reputed company
- Must be proficient with personal computer
- Ability to utilize keen judgment in evaluating information
- Ability to numerically and accurately reputed company and calculate test results in an electronic database
- Ability to work in a stressful environment
- Must be team oriented
- Prior Clinical research experience in a patient care setting preferred (Experience as an LPN or travel phlebotomist or clinical research experience preferred)
reputed company