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 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 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.

The Role

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 

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

OR

• • 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