The Company

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 15 clinical trial sites in the US and Canada and have rapid expansion plans.

This new Clinical Research Coordinator role will be based in Orlando, FL and is a full-time position.

You can read more about us at headlandsresearch.com.

The Role

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

 

The ideal candidate:

       Strong organizational skills

       Attention to detail

       Passionate about making a different in patients' lives

 

Duties

 

       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/LVN

OR

       Bachelor’s degree in a health or scientific related program

     A thorough understanding of regulatory requirements

     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