Clinical Research Nurse

Found in: Resume Library US A2 - 1 week ago


Chesterfield Missouri, United States Headlands Research Full time
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 in Missouri (RN or LPN/LVN)

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



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