Experienced Clinical Research Coordinator

Thank you for taking the time to read this ad. We have a great team and are looking for an experienced coordinator to join our team.

You must have a minimum of 3 years of experience as a Clinical Research Coordinator.

You must have experience checking and documenting vitals during the past year.

Phlebotomy is a plus.

You must have the authorization to work in the US for any employer.

You will not need visa sponsorship, either now or in the future.

We are seeking an experienced Clinical Research Coordinator to join our research team. You will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties required at the location.

On a day-to-day basis, you will:

• Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines

• Coordinate the operational aspects of a new and ongoing clinical trial at the site

• Work under the supervision of the Principal Investigator(s) while exercising excellent clinical judgment in patient monitoring and care

• Maintain daily contact with the Principal Investigator(s) for recruitment activities, study initiation, and general daily communication

• Responsible for the execution of the protocol as delegated by the Principal Investigator

• Prescreen and recruit research participants as directed by the central team

• Receive, dispense and log Investigational Product per protocol requirements

• Maintain and submit IRB communications and regulatory documents

• Communicate with internal teams, investigators, review boards, and study subjects

• Prepare other study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs

• Thoroughly understand ICH/GCP guidelines for human research subjects

• Computer competency, including Microsoft Office and EDC systems

• Other duties as assigned

To be successful in this role, you will bring:

• The position requires at least a High School Diploma, bachelor's degree or higher preferred

• At least  a minimum of 3 years experience as a Clinical Research Coordinator (requirement) 

• Must have Investigational New Drug (IND) or Investigational Product (IP) clinical trial experience.

• Ability to check and document vitals

• Phlebotomy experience is a plus

• Strong organizational skills

• Attentional to detail

• Ability to work independently but also collaboratively with team members

• Command of professional and Business English (written and spoken)

Preferred, but not required:

• Phlebotomy skills

• IATA Certification

• Ability to obtain EKG (ECG)