Summary The research coordinator I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes recruitment, screening, enrollment, randomization and management of the patient per the research protocol. The research coordinator I will collect data, patient reported outcomes, and questionnaires as required. The research coordinator I may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. The research coordinator I will collaborate with research coordinators, data managers and regulatory specialists. Other duties may be performed as assigned. Travel may be required. Responsibilities + Understands and knowledgeable of policies, procedures, and regulations governing human subject?s research and incorporates them in securing approval for and the conduct of research. + Implements, coordinates, manages and reports to the Institutional Review Board (IRB). + Implements, coordinates and manages clinical research operations. + Establishs and maintains communication with Investigators, research staff, study sponsors, research participants and their family members, and representatives of professional organizations associated with the conduct of the research. + Serves as an advocate for the human subjects by establishing and maintaining compliance in the conduct of the research protocol. + Actively identifies and participates in training, education and development activities to improve own knowledge and performance to sustain and enhance professional development. + Completes assigned goals. Requirements, Preferences and Experience Education Preferred: Associates's Degree or equivalent experience Minimum: High School Diploma Experience Preferred: 2 Years Research Experience Minimum: 2 years Lab, Medical and/or Research background Licensure, Registration, Certification Preferred: BLS Minimum: Special Skills Minimum: Computer skills to include MS Word, Excellent organizational skills. Detail oriented; Experience with EMR and Clinical Trials Management System Training Preferred: Knowledge of Medical Terminology About Baptist Memorial Health Care At Baptist, we owe our success to our colleagues, who have both technical expertise and a compassionate attitude. Every day they carry out Christ's three-fold ministry-healing, preaching and teaching. And, we reward their efforts with compensation and benefits packages that are highly competitive in the Mid-South health care community. For two consecutive years, Baptist has won a Best in Benefits award for offering the best benefit plans compared with their peer groups. Winners are chosen based on plan designs, premiums and the results of a Benefits Benchmarking Survey. At Baptist, We Offer: + Competitive salaries + Paid vacation/time off + Continuing education opportunities + Generous retirement plan + Health insurance, including dental and vision + Sick leave + Service awards + Free parking + Short-term disability + Life insurance + Health care and dependent care spending accounts + Education assistance/continuing education + Employee referral program Job Summary: Position: 20477 - Coordinator-Research I Facility: BMHCC Corporate Office Department: BCRI Baptist Clinical Research Category: Research Type: Non Clinical Work Type: Full Time Work Schedule: Days Location: US:TN:Memphis Located in the Memphis metro area REQNUMBER: 28555