Clinical Research Coordinator I

Job Description Job Description ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. 1) Comply with all company policies, procedures, and conduct. 2) Strictly adhere to confidentiality and compliance standards. 3) Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions. 4) Administer questionnaires and monitor participant compliance. 5) Acknowledge study patients' needs and tends to them appropriately. 6) Collect patient medical history and conditions. 7) Obtain Informed Consent. 8) Study drug dispensation records, accountability. 9) Liaison with laboratories to ensure timely participant testing 10) Collect and evaluate concomitant medication. 11) Collect and evaluate medical records for compliance. 12) Conduct A/E and SAE assessments. 13) Perform EKG, vital signs, nasal swabs and protocol specific procedures. 14) Evaluate clinical lab reports. 15) Maintain office site regulatory files. 16) Verify accuracy of data collected. 17) Document temperatures for IP stored on-site. 18) Assist with the recruitment and engagement of study subjects as needed. 19) Develop study e-source documents to comply with study protocol. 20) Manage all required study startup documentation, training, and timelines on assigned study protocols. 21) Meet all study protocol requirements and deadlines.