Overview

Clinical Research Professionals (CRP) is a dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through the advancement of new drug therapies and medical devices. We have recently partnered with the Headlands Research Network to provide best in class clinical trial services.

This is a full time position based at our office in St. Louis, MO

The Role

Clinical Research Professionals is looking for a Clinical Research Coordinator with a Nursing license to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.

Responsibilities

Comprehend study design of each protocol that is assigned
Obtain informed consent from study participants
Perform procedures in compliance with the study protocol
Screen study subjects according to specific protocol requirements
Collect and record study data in source documents via electronic system (CRIO)
Manage study related activities
Ensure adherence to protocol requirements
Review laboratory data
Assess and document compliance
Manage investigational product
Assess, record, and report Adverse Events as outlined in the protocol
Manage/train ancillary staff

Qualifications

Experience and training in conducting clinical trials with knowledge of ICH GCP
Licensed Nurse (LPN or RN) in Missouri
IV Certification, if LPN
Degree in a health or scientific related program strongly preferred
Excellent interpersonal and communication skills: Able to interact effectively with professional and administrative staff, sponsor and regulatory representatives.
Compassion for patients (study participants)
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing lab specimens
Excellent written & oral communication skills
Have a passion for clinical research and helping people
Experience with CRIO (Clinical Trial Management System) is a plus
Experience with administering vaccines is a plus

Headlands Research

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Clinical Research Coordinator