Clinical Research Coordinator Position Available In Orange, Florida
Tallo's Job Summary: The Clinical Research Coordinator position at Headlands Research Orlando involves managing clinical research protocols, ensuring compliance with ICH GCP guidelines, recruiting and screening study subjects, collecting and recording study data, and managing study-related activities. Qualifications include experience in clinical trials, knowledge of ICH GCP, familiarity with IRB submissions, and excellent interpersonal and communication skills. The company operates multiple clinical trial sites in the US and Canada with plans for expansion.
Job Description
Clinical Research Coordinator
Job Locations
US-FL-Orlando
ID 2025-1873
Category Clinical – Staff Position Type Regular Full Time
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
