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Human Studies Research Coordinator Creation Health Research Orlando

Orlando, FL

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Human Studies Research Coordinator – Creation Health Research – Orlando Orlando seeks to hire a Human Studies Research Coordinator who will embrace our mission to extend the healing ministry of Christ. Facility Profile: Located on a lush tropical campus, our flagship hospital, 1,107-bed Florida Hospital Orlando, serves as the major tertiary facility for much of the Southeast, the Caribbean and South America. Florida Hospital Orlando houses one of the largest Emergency Departments and largest cardiac catheterization labs in the country. We are already one of the busiest hospitals in the nation, providing service excellence to more than 32,000 inpatients and 125,000 outpatients each year. Department Profile: The Creation Health Research is the product of an innovative affiliation between Florida Hospital and Sanford-Burnham Medical Research Institute that bridges the gap between discovery research and clinical care. The TRI brings together the complementary strengths of Sanford-Burnham's basic science prowess and advanced research technologies and Florida Hospital's compassionate, comprehensive clinical care and clinical/translational research expertise to accelerate the discovery and development of new approaches to diagnose, treat, and prevent obesity, diabetes, and their cardiovascular complications. Work Hours/Shifts: M-F, 8a-5p Job Summary: Under limited supervision, the Human Studies Research Coordinator plans, coordinates, and manages study protocols and data for assigned research projects. Follows study specific protocol guidelines; communicates and interacts with investigators, hospital staff, sponsoring agencies, and others to effectively perform clinical research; and coordinates research activities. This role includes research subject advocacy and education, education of other personnel, and marketing and promotion of the research platform. Abides by hospital and departmental policies and SOPs, as well as all applicable local, state, and federal regulations. Actively participates in outstanding customer service and accepts personal responsibility in maintaining relationships that are equally respectful to all. Knowledge, Skills, Education, & Experience Required: BS in health-related field, OR Bachelors degree in Science or Biology OR 4 years experience coordinating research data and projects in the biomedical field Specialized knowledge of the current internal and external regulatory needs of clinical trials Personal qualities and interpersonal communication skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances Detail oriented and teamwork skills Motivated, organized, able to perform multiple tasks in a timely manner, and work efficiently under pressure Ability to manage multiple clinical trials and function independently Critical thinker and possess an analytical approach to problem solving Ability to perform diverse administrative duties Expert knowledge of Microsoft Office applications of Word, Excel, Access, Outlook, and Internet Ability to adapt own approach according to investigator's level of expertise to assure all institutional needs are met while learning occurs Prior research experience (preferred) Licensure, Certification, or Registration Required: Certificate from Clinical Research professional organization, i.e. SOCRA, ACRP (preferred) Job Responsibilities: Demonstrates through behavior Florida Hospital's Core Values of Integrity, Compassion, Balance, Excellence, Stewardship and Teamwork as outlined in the organization's Performance Excellence Program Responsible for maintaining professional knowledge and growth, as well as, contributes to the growth of team members. Responsible for confirmation of eligibility and enrollment of patients upon referral. Responsible for reviewing all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA, NCI, and state, federal and institutional regulations with study candidates and/or legal representative. Provides administrative support to department by providing research meeting coordination, taking meeting minutes, and coordinating necessary travel arrangements with a high level of accuracy and good judgment. Responsible for database construction with input from department director Provides administrative support to department by assisting with policy and procedure development and annual updates, upkeep of regulatory binders, and filing. Provides administrative support to department by conducting data entry into established databases with a high level of accuracy. Demonstrates through human subject advocacy and informed consent as an ongoing process, that the rights, safety, and well-being of trial subjects are the most important considerations and should prevail over the interests of science and society. Responsible for special projects as assigned by department director Responsible for the immediate oversight of the study conduct during the pre-study, active and follow up phase, for all assigned studies. Responsible for accurate and timely submission of data forms for assigned studies. Responsible for communication across a wide variety of internal hospital departments and the principal investigators (PI) of assigned studies. Promotes PI oversight by advising the PI, sub-investigator, and immediate supervisor of deviations in conduct, subject or study status, issues relevant to the integrity of the trial and/or the safety of research subjects) If you want to be a part of a team that is dedicated to delivering the highest quality in patient care, we invite you to explore the Human Studies Research Coordinator opportunity with Orlando and apply online today. Job Keywords: Research, Coordinator, Orlando   ,@type:JobPosting,responsibilities:,validThrough:2018-08-12T04:00:00Z,title:Human Studies Research Coordinator – Creation Health Research – Orlando,datePosted:2018-07-13T06:58:44Z}

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