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 Stockbridge GA

This opening is for Monday-Thursday and is a full time position

You can read more about us at headlandsresearch.com.

The Role

CRA Headlands/Clinical Research Atlanta 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:

      Has 3 or more years experience conducting clinical trials. Vaccine trials are a plus

      Has an understanding of an unblinded role in a clinical trial and is licensed to give vaccines in the state of Georgia. (Registered Medical Assistant, LPN, RN)

      A multi-tasker that has the ability to think “out-side the box” and to be able to work with a team in a fast paced environment

      Has a thorough understanding of quality and protocol adherence

      Detail-oriented

 

Duties

 

        Comprehend study design of each protocol that is assigned both from a typical coordinator role as well as the unblinded staff role

        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 & protocol deviations as outlined in the protocol

        Manage/train ancillary staff

        Prepare/maintain accountability records

        Meet with monitors/physicians/staff members

 

 

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

This position has been filled. Would you like to see our other open positions?