Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via emailJob Duties:
Assist in recruitment and educating potential research participants evaluating potential eligibility for investigatorinitiated and/or industrysponsored studies.
Participate in Informed Consent Interviews with participants and study partners as delegated by the Principal Investigator based on level of training and experience.
Obtain medical records when appropriate following all institutional policies.
Assist in collection and processing of biological specimens as outlined in the protocol and following institutional policies.
Assist in the collection of study data within the scope of role and experience under the supervision of the study coordinator.
Track and document studyrelated activities in a timely and accurate manner as directed.
Assist with maintaining adequate study supply inventory for the conduct of study visits.
Assist with study visit activities including scheduling visits and procedures within protocol specified parameters.
Assist in entering collected data into sponsors electronic databases within required timeframes and respond to database queries in a timely manner.
Assist with timely and thorough filing of regulatory documents in Investigator Site Files.
This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.
Education: Associates degree or an equivalent combination of relevant postsecondary education and work experience that equals at least 2 years.
Preferred Qualifications
Education: Bachelors degree in a relevant field is highly preferred.
Work Experience: Experience in health care in a patient setting and/or clinical research experience.
Skills:
Attention to detail time management and organizational skills
Interpersonal skills.
Required Documents:
Comprehensive Benefits Package:
Coverage begins on day one for health dental and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employerpaid life insurance longterm disability insurance and various additional voluntary insurance plans are available. Paid time off including vacation and sick begins accruing upon hire plus ten paid holidays. One paid discretionary day is available after six months of employment and paid time off for bereavement jury duty military service and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. Type: Regular Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including but not limited to education experience and training qualifications relative to the requirements of the position and funding. At the University of Kansas Medical Center a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range taking into account the combination of factors listed above. Minimum Midpoint MaximumTime Type:
Full timeRate Type:
HourlyPay Range:
$22.66 $32.85
Full-Time