WI3662777

1

Unspecified

40

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. With over 19,000 staff conducting operations in more than 90
countries, Fortrea is transforming drug and device development for
partners and patients across the globe. Operations Coordinator I
Full-Time, on site in Madison, WI Responsible for
practical/administrative activities in support of a clinical research
trial. The Operations Coordinator I supports and assists the senior
study team members such as the Clinical Research Coordinator and Project
Manager as appropriate. 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\... 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/F751DBFAB494469B