Clinical Research Coordinator

Headlands Research Scottsdale!; Orlando (FL); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading clinical trial site in Orlando is seeking a Clinical Research Coordinator to oversee clinical research protocols. This role involves managing study activities, ensuring compliance with guidelines, and interacting with various stakeholders. The ideal candidate will have a background in health sciences and excellent communication skills.

Qualifications

• Experience and training in conducting clinical trials with knowledge of ICH GCP.
• Familiarity with IRB submissions.

Responsibilities

• Manage clinical research protocols and ensure compliance with ICH GCP guidelines.
• Recruit and screen study subjects according to specific protocol requirements.
• Collect and record study data in source documents.

Skills

Interpersonal Skills

Communication Skills

Clinical Assessments

Education

Bachelor’s degree in a health or scientific related program

Two years of college in a health-related program or LPN

Tools

CRIO

Job description

Overview

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 20+ clinical trial sites in the US and Canada with rapid plans for expansion.

The Role

Headlands Research Orlando is looking for a Clinical Research Coordinator 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
• Perform procedures in compliance with the study protocol
• Recruit and screen study subjects according to specific protocol requirements
• Collect and record study data in source documents via electronic system (CRIO)
• Manage study related activities
• 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

Education:

• Experience and training in conducting clinical trials with knowledge of ICH GCP

OR

• Two years of college in a health-related program or LPN

OR

• Bachelor’s degree in a health or scientific related program
• A thorough understanding of regulatory requirements/eReg
• Familiarity with IRB submissions.
• Excellent interpersonal and communication skills: Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
• Experience with CRIO (Clinical Trial Management System) is a plus
• Experience with administering vaccines is a plus