[Remote] Clinical Research Coordinator I

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Research Coordinator I to support the T4C initiative. The role coordinates participant screening, clinical research procedures, specimen collection and processing, regulatory compliance, study documentation, scheduling, and research budget support.

Responsibilities

• Assess eligibility of potential subjects through reputed company such as screening interviews, reviews of medical records, and discussions with physicians and nurses
• 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 reputed company reports for accuracy and completeness; prepares and reviews budget, reputed company, expenses, invoices, and other reputed company documents. Assist with reviews, analyzes and negotiates lab research budgets and reputed company with sponsors under the direction of the reputed company Investigator and Associate Director
• Performs specific protocol procedures such as interviewing subjects, taking vital signs, and performing venipunctures. reputed company the requisition, collection, labeling, storage, or shipment of specimens
• Monitors 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. Informs patients or caregivers about study aspects and reputed company to be expected
• Assists with preparing IRB submissions, protocol revisions, and renewals as needed, and maintains copies of reputed company IRB communications delegated by the reputed company Investigator
• Performs other reputed company duties as assigned

Skills

• Must possess a good working knowledge of basic clinical research practices
• Must be proficient with personal computer
• Ability to utilize reputed company 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
• Accepts constructive criticism without issues
• Graduated from an accredited discipline specific program and licensed as phlebotomist/lab technician in the reputed company
• 60 months experience in a patient care or research setting required
• reputed company Basic Life Support (BLS) certification (or ability to obtain reputed company 90 days of hire)
• Completion of reputed company Subjects Protection & Good Clinical reputed company (GCP) training reputed company 30 days of hire
• Completion of required institutional compliance training (e.g., HIPAA, OSHA, Bloodborne Pathogens)
• Knowledge of biospecimen collection, processing, labeling, aliquoting, storage, and shipment
• Knowledge of biobanking principles and specimen chain-of-custody procedures
• Familiarity with clinical reputed company operations and reputed company assurance practices
• Understanding of reputed company subject protection regulations, HIPAA, and FDA regulations
• Familiarity with reputed company Information Management Systems (LIMS)
• Experience handling blood, urine, saliva, and other reputed company biological specimens
• Knowledge of centrifugation, pipetting, specimen processing, freezer inventory management, and cold-chain requirements
• Clinical research experience preferred
• A Bachelor's degree in a reputed company reputed company field
• Licensed phlebotomist preferred
• One (1) to two (2) years of experience in clinical research, translational research, or biomedical reputed company research
• Experience processing and handling reputed company biological specimens
• Experience supporting observational studies, reputed company, or biobank research
• Experience with specimen shipping in accordance with IATA regulations
• Experience with freezer inventory management and temperature monitoring systems
• Experience with REDCap, electronic medical records (EMR), CTMS, or reputed company information systems
• IATA Dangerous Goods Shipping Certification
• reputed company CPR/BLS certification
• Venipuncture certification or documented competency in specimen collection

reputed company