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Location
Cincinnati, OH, United States
Posted on
Oct 01, 2021
Profile
CURRENT UC EMPLOYEES MUST APPLY INTERNALLY VIA SUCCESSFACTORS > ****
Founded in 1819, **MEMBERS ONLY**SIGN UP NOW***. embarks upon its third century - building on the past and defining the future by leading urban, public universities into a new era of innovation and impact through its strategic direction, Next Lives Here. Underscoring the power of creativity, ingenuity, invention and inclusion, what's Next will accelerate our unrivaled momentum, evidenced by eight straight years of record enrollment and rankings that include placement among America's top 100 public universities by U.S. News & World Report. Home to a diverse student body of nearly 47,000 and more than 4,200 distinguished faculty, the university combines its Research 1 (Very High Research Activity) Carnegie Classification with a physical setting that The New York Times recently acclaimed as the most ambitious campus design program in the country.
JOB OVERVIEW
The College of Medicine, Department of Internal Medicine, Division of Endocrinology, Diabetes and Metabolism is currently accepting applications a full time, Clinical Research Professional, to assist with trials.
This position will support the University's mission and commitment to excellence and diversity in our students, faculty, staff and all our activities.
ESSENTIAL FUNCTIONS
STUDY COORDINATION
*Assist in planning and implementing the clinical study's goals and objectives; organize study participant enrollment planning; conduct quality assurance activities; compile and analyze data *Coordinate nursing and participant care and/or participant follow-up functions of the clinical study including planning and developing related activities. *Develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected. *Act as a liaison with medical staff, University Departments, ancillary departments and/or satellite facilities
NURSE COORDINATION
*Provide quality care to study participants and their families within area of clinical specialty *Enroll and follow large caseload of study participants, from screening visit through end of study, on multiple studies as assigned *May serve as a resource person or act as a consultant within area of clinical expertise *Promote continuity of care through consultations with participants, families, medical and nursing staff *Perform complex physical/clinical procedures *Initiate and/or assist with developing and revising policies and procedures for nursing practice
ADMINISTRATION (WORK IN CONJUNCTION WITH DOIM RESEARCH FINANCIAL SERVICES)
*Demonstrate a comprehensive understanding of contract principles, federal regulations, laws and UC/UCPC policy and operating procedures. *Work closely with UC and UC Health offices in negotiation of contracts, confidentiality agreements and amendments related to the conduct of research activities. *Work with necessary parties to identify compliance, legal, IP and business/financial risk. Mitigate risk through working with physicians/faculty, divisions, legal and/or other departments. *Prepare, develop, review and negotiate industry and sponsored research clinical trial budgets for consistency with UC/UCPC policies and operating procedures. *Effectively negotiate budgets to obtain funding sufficient to successfully execute research as applicable.
REGULATORY (WORK IN CONJUNCTION WITH DOIM RESEARCH REGULATORY SERVICES)
*Prepare, submit, and assist Director with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms). *Maintain regulatory documentation. *Prepare and maintain FDA applications for INDs. *Serve as resource person or act as consultant within area of regulatory expertise. *Conduct internal audits. *Make and assist in modifying protocols and study documents. *Write reports, business correspondence, and procedure manuals.
DATA ENTRY/MANAGEMENT
*Perform quality checks on data entered by others. *Assist with creation of case report forms. *Database creation, testing, and basic maintenance. *Act as liaison between study personnel and data entry specialists. *Create data entry instructions and train data entry specialists. *To ensure the continued success and growth of unit, participate fully as a vital member of the Research Team: *Attends meetings as assigned *Completes continuing education and training programs as assigned on continual basis, in addition to continuing education required for licensure renewal *Other duties as delegated/assigned
Other duties as delegated/assigned by the Clinical Research Director or Principal Investigator
REQUIRED EDUCATION
*Bachelor's Degree must be in a related field. *Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.
REQUIRED TRAININGS/CERTIFICATIONS
*For nursing focused role, BSN in the area of clinical specialization, and RN License in State of Ohio. *For social work focused role, licensure in the area of clinical specialization.
REQUIRED EXPERIENCE
*One (1) year of related experience. *For nursing focused roles, appropriate clinical procedural experience.
ADDITIONAL QUALIFICATIONS CONSIDERED
*Excellent oral and written communication skills *Meticulous source documentation skills *Proficiency in various computer and software applications is ideal *Endocrinology, Diabetes & Metabolism experience strongly ideal but not required
PHYSICAL REQUIREMENTS/WORK ENVIRONMENT
*Sitting - Continuously
COMPENSATION AND BENEFITS
UC offers a wide array of complementary and affordable benefit options, to meet the financial, educational, health, and wellness needs of you and your family. Eligibility varies by position and FTE.
*Competitive salary range dependant on the candidate's experience. *Comprehensive insurance plans including medical, dental, vision, and prescription coverage. *Flexible spending accounts and an award-winning employee wellness program, plus an employee assistance program. *Financial security via our life and long-term disability insurance, accident and illness insurance, and retirement savings plans. *Generous paid time off work options including vacation, sick leave, annual holidays, and winter season days in addition to paid parental leave. *Tuition remission is available for employees and their eligible dependents. *Enjoy discounts for on and off-campus activities and services.
**MEMBERS ONLY**SIGN UP NOW***., as a multi-national and culturally diverse university, is committed to providing an inclusive, equitable and diverse place of learning and employment. As part of a complete job application you will be asked to include a CONTRIBUTION TO DIVERSITY AND INCLUSION statement.
As a UC employee, and an employee of an Ohio public institution, if hired you will not contribute to the federal Social Security system, other than contributions to Medicare. Instead, UC employees have the option to contribute to a state retirement plan (OPERS, STRS) or an alternative retirement plan (ARP).
**MEMBERS ONLY**SIGN UP NOW***. IS AN AFFIRMATIVE ACTION / EQUAL OPPORTUNITY EMPLOYER / MINORITY / FEMALE / DISABILITY / VETERAN.
REQ: 72641
SF:OMJ SF:RM SF:HEJ, SF:INS SF:HERC SF:DIV SF:LJN
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