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 18 clinical trial sites in the US and Canada with rapid plans for expansion.  

The Role

Pharmasite, a Headlands Research site, 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

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