At Headlands Research, we are building the best clinical trial company in the world. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, our company is in high growth mode; we operate 12 clinical trial sites in the US and Canada and have rapid expansion plans.
This new Clinical Research Coordinator role will be based in Atlantis, FL (West Palm Beach area).
This opening is for Monday - Friday and is a contract (1099) position.
You can read more about us at headlandsresearch.com.
JEM Research Institute 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.
The ideal candidate:
Superior interpersonal and communication skills
Have a heightened sense of responsibility
Is a team player
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
Experience and training in conducting clinical trials with knowledge of ICH GCP
Two years of college in a health-related program or LPN
Bachelor’s degree in a health or scientific related program
A thorough understanding of regulatory requirements
Knowledgeable of Regulatory Binder maintenance, delegation of duties, training requirements, and understanding of approval documents filing.
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