Posted in Other 30+ days ago.
Type: Full Time
DESCRIPTION SHIFT: No Weekends
SCHEDULE: Full-time
DO YOU HAVE THE CAREER OPPORTUNITIES YOU WANT IN YOUR CURRENT ROLE? WE HAVE AN EXCITING OPPORTUNITY FOR YOU TO JOIN THE NATION\'S LARGEST PROVIDER OF HEALTHCARE SERVICES AS A CLINICAL COORDINATOR - LICENSED.
HCA Healthcare is a national leader in providing modern, culturally competent, patient-centered care and we are driven by a single goal: THE CARE AND IMPROVEMENT OF HUMAN LIFE.
We offer you an excellent total compensation package, including competitive salary, excellent benefit package and growth opportunities. We believe in our team and your ability to do excellent work with us. Your benefits include 401k, PTO medical, dental, flex spending, life, disability, tuition reimbursement, employee discount program and employee stock purchase program. We would love to talk to you about this fantastic opportunity.
The HCA Physician Services Group (PSG) is the physician and practice management solution for HCA Healthcare. We lead a collection of highly motivated healthcare professionals just like you and creative leaders who are committed to excellence in every patient interaction. Are you excited yet?
CLICK HERE to learn more
Seeking a CLINICAL COORDINATOR - LICENSED for our practice who provides clerical expertise to ensure all patients receive high quality, efficient care. We are an amazing team that works hard to support each other and are seeking a phenomenal addition like you who feels patient care is as meaningful as we do. We want you to apply now.
WHAT YOU WILL DO IN THIS ROLE:
Coordinate research-related activities with clinical and non-clinical staff throughout the health system.
Assist in ensuring that all new employees are oriented to the program.
Provide education, orientation and in-services for the program staff when deficits in clinical knowledge are identified.
Provide supervision and direction to any clinical trials assistants or other delegates of the Principal Investigator.
Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements.
Promote organization to private industry or governmental sponsors of clinical trials.
Assists in preparing study contracts and budgets.
Obtain detailed knowledge of all components of study protocol through independent analysis and review of study to complete all study activities completely.
Attend mandatory educational programs (i.e. Investigator Meetings) which may include traveling to different cities.
Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor.
Use time constructively and in an organized manner to accomplish assigned responsibilities.
Screen patients and/or their medical records and identify potential subjects for a specific study on a timely basis and within the recruitment period.
Ensure that all subjects meet protocol requirements by utilizing inclusion/exclusion criteria.
Ensure that an original copy of any subjects Informed Consent Document is in the research binders, as well as, a copy on the subject's medical record.
Schedule all subject visits and procedures to meet protocol requirements. Provide instructions and pertinent dates to ensure proper protocol compliance.
Ensure that all protocol activities are performed by approved research staff.
Ensure that all laboratory samples are collected and processed properly and a timely basis.
If adequately licensed, distribute study medications and perform medical procedures according to the protocol requirements.
Report to the IRB and any research sponsors any and all adverse events experience by he subject.
Server as a liaison between the subject and their care giver.
Serve as the primary contact with the research sponsor.
Serves as the internal expert regarding all study protocols.
Serves as the internal expert on clinical research regulatory matters.
Practice and adhere to the \\"Code of Conduct\\" philosophy and \\"Mission and Value Statement\\".
QUALIFICATIONS
WHAT QUALIFICATIONS YOU WILL NEED:
EDUCATION:
No education requirements
EXPERIENCE:
Minimum of two to three solid years of medical office experience in a supervisor or lead role.
Proven performance in solving operational issues within a healthcare setting.
Proven performance leading a successful team in a fast paced healthcare setting.
CERTIFICATION/LICENSE:
Certification by the Association of Clinical Research Professionals is preferred or working towards certification.
HCA Healthcare ranks on Fortune's list of Most Admired Companies for three consecutive years and HCA ranks 63rd on the Fortune 500 list. In addition, Ethisphere named HCA as one of the World's Most Ethical Companies. We want you to join our tradition of excellence. Intrigued? We'd love to hear from you.
If you find this opportunity compelling, we encourage you to apply. We promptly review all applications. If you are highly qualified, you will hear from one of our Practice Managers. We are actively interviewing so apply today.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
NOTICE
Our Company's recruiters are here to help unlock the next possibility within your career and we take your candidate experience very seriously. During the recruitment process, no recruiter or employee will request financial or personal information (Social Security Number, credit card or bank information, etc.) from you via email. The recruiters will not email you from a public webmail client like Gmail or Yahoo Mail. If you feel suspicious of a job posting or job-related email, let us know by clicking here.
For questions about your job application or this site please contact HCAhrAnswers at 1-844-422-5627 option 1.
|
Kroger |
|
Kroger |
|
Kroger |