WI3818910

1

High School Diploma/GED

High School Diploma/GED Equivalent

Unspecified

40

JOB REQUIREMENTS: Position Description: Purpose Assist study
coordinators by providing administrative and data collection support for
clinical research studies. Primary Functions Under direction of the
study coordinator or principal investigator, conduct research activities
to include visit study participant homes, community centers and other
community settings to interview, administer surveys, recruit, and enroll
and follow-up with study participants as directed. Under direction of
the CTO research manager, study coordinator/research nurse and principal
investigator, conduct research activities to include enrollment to
non-interventional trials and complete follow-up with study participants
as directed. Contact study participants to obtain research related data.
Under the direction of appropriate research manager and
Education/Quality Assurance Manager assist in training as mentor for new
CRA IIs in CTO. Coordinate patient visits to clinic. Organize study
participant charts and files, and distribute to appropriate location.
Coordinate research related projects such as mailings, participant
contact information, patient visits and focus groups. Collect required
data from study coordinators and research nurses. Code and enter onto
clinical research forms and into computerized database. Collect required
data from study coordinators and research nurses and other sources
including EPIC as directed and accurately enter research data onto case
report forms or specified programs (OnCore) and other databases as
appropriate under the direction of the research nurse or study
coordinator. Prepare specimen tubes prior to lab draw and transport
specimens from lab to process and send out areas as necessary working
with CTO processing lab assistant. Assist with processing of lab
specimens in preparation for send out or storage as requested in
conjunction with CTO processing lab assistant. Prepare shipping labels
and document labels for both data and specimens. Under the supervision
of the research manager, research nurse, study coordinator or
investigator, assist in enrolling patients on biospecimen trials. May
converse with patients as required after intitial contact to obtain
additional information. Under special circumstances may obtain informed
consent after sign off on that competency. Under the direction of the
research nurse, study coordinator or principal investigator, enroll
patients in educational and social intervention research studies.
Contact patients as required after intitial contact to obtain additional
information. Under special circumstances may obtain informed consent
after sign off on that\... For full info follow application link. EEO/AA
Minorities/Females/Vets/Disability The Medical College of Wisconsin is
an affirmative action/equal opportunity employer and does not
discriminate in hiring or employment on the basis of age, sex, race,
color, religion, national origin, veteran status, disability or sexual
orientation. \*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/440C02D31F9542FF Qualified females, minorities, and special
disabled veterans and other veterans are encouraged to apply.