Clinical Trials Research Data Coordinator - Cancer Center

The Holden Comprehensive Cancer Center at the University of Iowa is seeking a Clinical Trials Research Data Coordinator to assist in the planning, delivery and evaluation of health care provided to research protocol patients.

This position will work closely with Clinical Research Coordinators in the collection of data and in close collaboration with multiple departments and offices, including the University Clinical Trials Office;

maintain medical documentation, binders and files; manage data entry and electronic data systems for clinical research protocols currently being conducted within the Holden Comprehensive Cancer Center (HCCC) at The University of Iowa.

Duties to include :

• Reviewing patient charts, lab reports, study worksheets and other related information to obtain data required per protocol
• Enters protocol-required patient data into electronic databases ensuring that all assessments are completed, and data conforms to database required fields
• Responds to sponsor-initiated queries relating to the data entered and proactively works to keep data clean for end of study analysis.
• Enters and maintains institutional-required patient data in Clinical Trials Management System, OnCore.
• May assist in the developmentof worksheets, treatment flow sheets and assorted tools to provide source documentation of protocol treatment procedures;

provides follow-up for treatment related complications

• Timely Communication regarding gaps in data collection and reporting needs
• Assists in the organization and preparation of research study charts for periodic review by both internal and external monitors and auditors.
• Assist in follow up of any queries identified in the review
• Coordinate the scheduling of on-site and remote monitoring visits, audits, and study start up visits
• Assist in obtaining access to electronic medical and regulatory records for the monitor’s visit
• May obtain documentation of external hospitalizations or reports from treatment at external facilities
• Attends protocol meetings and other UIHC and Study Sponsor meetings; participates on committees as appropriate

UI Health Care Core Values (WE CARE)

W elcoming

We are welcoming to the community, partners, staff, and patients utilizing the collective strength of our people.

E xcellence

Excellence for us is judged by Are we one of the top hospitals in the country in quality, safety, patient satisfaction, and employee satisfaction?

C ollaboration

We believe teamwork is the best way to work.

A ccountability

We behave ethically, act openly and with integrity in all that we do, taking responsibility for our actions.

R espect

We honor diversity and recognize the worth and dignity of every person.

E quity

We believe that without the diversity of experience, background, through that we have, we cannot deliver excellent and innovative care.

SUPERVISION RECEIVED :

Supervision of the data coordinator role is provided by the Data Coordinator Supervisor

SUPERVISION EXERCISED :

Functional direction and supervision may be provided over assigned support staff.

University of Iowa Hospitals & Clinics recognized as one of the best hospitals in the United States is Iowa's only comprehensive academic medical center and a regional referral center.

Each day more than 12,000 employees, students, and volunteers work together to provide safe, quality health care and excellent service for our patients.

Simply stated, our mission is : Changing Medicine. Changing Lives.®

Holden Comprehensive Cancer Center is Iowa’s only NCI-designated comprehensive cancer center. The NCI designation recognized our cancer center, and its research scientist, physicians, and other health care professionals, for their roles in advancing cancer research that impacts on our ability to prevent, detect and treat our patients with cancer.

Not just a floor, or a building, or even confined to a single college. Holden Comprehensive Cancer Center coordinates all cancer-related research, education, and patient care by faculty from 41 departments and six colleges, as well as UI Hospitals and Clinics and UI Children’s Hospital.

Percent of Time : 100%

Pay Grade : 3A

Benefits Highlights :

• Regular salaried position located in Iowa City, Iowa
• Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
• For more information about Why Iowa?, click

Required Qualifications

• Bachelor’s degree or an equivalent combination of education and experience
• 6 to 12 months experience in a research or health care setting
• Experience with medical terminology
• Excellent verbal, written and interpersonal communication skills
• Proficient in computer software applications
• Ability to manage complex information with attention to detail and a high level of accuracy

Desirable Qualifications

• Relevant experience in the conduct of clinical or laboratory research studies
• Knowledge of regulatory guidelines and procedures
• Clinical Research Coordinator Certification (SOCRA or ACRP)
• Certification that allows for blood draw (Phlebotomy Technician, Certified Medical Assistant, LPN)
• Experience conducting electrocardiograms (ECG)
• Experience working with Epic
• Experience working with OnCore Clinical Trials Management System
• Knowledge of University of Iowa policies, procedures and regulations

Application Process : In order to be considered, applicants must upload a resume and cover letter (under submission relevant materials) that clearly address how they meet the listed required and desired qualifications of this position.

Job openings are posted for a minimum of 14 calendar days.

Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential / education verification.

References : Five professional references will be requested and required at a later step in the recruitment process

This position is not eligible for University sponsorship for employment authorization.

With additional questions, please reach out to Sarah Waldschmidt at

Additional Information

• Classification Title : Clin Trials Rsrch Asst / Data Mg
• Appointment Type : Professional and Scientific
• Schedule : Full-time

Compensation

Pay Level : 3A

Contact Information

• Organization : Healthcare
• Contact Name : Sarah Waldschmidt
• Contact Email : [email protected]
30+ days ago