Clinical Research Assistant - Internal Medicine (Medical Oncology)

Description

Job Duties

Research data collection and entry.

Administrative support for licensure and credentialing, general paperwork, scheduling, procurement, and correspondence.

Provide administrative assistance to Principal Investigator.

Assist in editing and formatting of grant proposals and manuscripts.

Assist in maintaining regulatory paperwork for research studies.

Recruit, evaluate, and educate patients regarding clinical trials following established procedures and protocols.

Conduct informed consent interviews with participants.

Document trial related activities as directed and ensure study data is reported in a timely and accurate manner.

Coordinate study participant visit activities including scheduling procedures, communicating with subjects, and completing necessary basic study procedures.

Assist with transport or shipping of research biological specimens between clinical trial sites.

Provide written and verbal reports to the Principal Investigator and Program Director, as required.

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.

Required Qualifications

Education : Bachelor’s degree in biology, genetics, pre-med, or related field. Education may be substituted for experience on a year for year basis.

Preferred Qualifications

Experience in biomedical research (including any internship, educational, or volunteer experience).

Prior cancer-related knowledge.

Basic understanding of regulations governing clinical research (e.g. GCP, HIPAA).

Experience with electronic medical records.

Experience with Endnote and PubMed.

Proficiency with Microsoft Excel.

Skills

Detail-oriented, self-motivated, and possess good interpersonal skills.

Strong work ethic.

Advanced beginner skill or competency in Microsoft Word, Excel, PowerPoint, and Outlook. Ability to learn new software and systems.

Excellent communication; oral and written.

Ability to contribute to a project team setting.

Integrity and respect for patient confidentiality.

Required Documents

Resume / CV

Cover Letter that highlights your relevant work or research experience.

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. Employer-paid life insurance, long-term 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.

Employee Type : Regular

Time Type : Full time

Rate Type : Hourly

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.

Pay Range : 22.66 - $32.85

Minimum

22.66

Midpoint

27.75

Maximum

32.85

Salary : $23 - $33