Job Information
Job Order ID :
WI3817283
# of Positions :
1
Experience Required :
Duration :
Shift :
Unspecified
Hours per week:
40
Job Description
JOB REQUIREMENTS: As a leading global contract research organization
(CRO) with a passion for scientific rigor and decades of clinical
development experience, Fortrea provides pharmaceutical, biotechnology,
and medical device customers a wide range of clinical development,
patient access, and technology solutions across more than 20 therapeutic
areas. Conducting operations in \~100 countries, Fortrea is transforming
drug and device development for partners and patients across the globe.
Operations Coordinator I Office based in Madison, WI Job Overview:
Responsible for practical/administrative activities in support of a
clinical research trial. The Operations Coordinator II supports and
assists the senior study team members such as the Clinical Research
Coordinator and Project Manager as appropriate. Summary of
Responsibilities: Responsible for logistical set up of study to ensure
good study flow and adequate resources are assigned. Assists the
Clinical Research Coordinator with their responsibilities and acts as
their back-up as needed. Assists and/or is responsible for the creation
of source documents, labels, and study specific instructions. Assists
and/or is responsible for creation of study schedules. Orders
supplies/equipment and dietary needs for assigned studies. Liaises with
CRU contracted services, such as clinical labs and ECG services. Assists
and/or is responsible for staff training of study specific procedures.
Coordinates tasks related to participant check in and discharge and may
assist with resolution of participant issues. Is present in the clinical
work areas for critical events or as assigned by a senior team member.
Completes sample shipment documentation as necessary. May assist with
sample shipments as needed. Compiles data tables/summaries as requested.
Assists with on-time CRF completion and query process as appropriate.
Assists with the compilation of protocol and SOP deviations. Provide
logistical feasibility for protocol development. Attends all required
meetings as appropriate. Maintains skills to perform study tasks and
assists with study procedures as necessary. Maintains accurate records
of all work undertaken. Maintains an understanding of FDA, GCP and ICH
requirements. Maintains constant\... For full info follow application
link. As an EOE/AA employer, Fortrea strives for diversity and inclusion
in the workforce and does not tolerate harassment or discrimination of
any kind. We make employment decisions based on the needs of our
business and the qualifications of the individual and do not
discriminate based upon race, religion, color, national origin, gender
(including pregnancy or other medical conditions/needs), family or
parental status, marital, civil union or domestic partnership status,
sexual orientation, gender identity, gender expression, personal
appearance, age, veteran status, disability, genetic information, or any
other legally protected characteristic. We encourage all to apply.
\*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/A0351D1F9FBC4693
Company Information
Name :
FORTREA INC.
Application Information