Fortrea

Study Coordinator II / Madison, WI (On-site)

Madison · Mid · Part-time

Sponsorship not specifiedDetected 15 days ago

GCPData AnalysisProject ManagementExcelClinical TrialsClinical ResearchFDA RegulatoryMedical DevicesResearchMicrosoft Office

About the role

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.
If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Orders supplies/equipment and dietary needs for assigned studies. - Liaises with CRU contracted services, such as clinical labs and ECG services.

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.
Assists and/or is responsible for the creation of source documents, labels, and study specific instructions.
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.
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 awareness of participant safety and dignity at all times.
Takes ownership for the quality and standard of own work.
Performs other related duties as assigned.

Must be able to sit at a computer for long periods of time.
Must be able to use hands to finger, handle or touch objects, tools, or controls, including a computer keyboard, for up to 8 hours per day.
Will involve out of normal office hours as required by the role.
Attends all required meetings as appropriate.

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
Paid time off (PTO)

We are currently seeking a Study Coordinator II, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment.
Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time, office/clinic-based job in Madison, WI.

This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.