Clinical Research Coordinator

Overview

Coordinate clinical trial operations, patient recruitment, and regulatory compliance.

Key Responsibilities

• protocol execution
• patient monitoring
• document prep
• irb submissions
• patient recruitment
• trial management

Tasks

-Execute the protocol and ensure that all staff working on any given protocol are properly delegated by the Principal Investigator and adequately trained. -Work under the supervision of the Principal Investigator(s), exercising excellent clinical judgment in patient monitoring and care. -Prepare study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs. -Maintain and submit IRB communications and regulatory documents. -Recruit and pre-screen patients for the study. -Maintain daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general communication. -Communicate in a timely manner with internal teams, investigators, review boards, and study subjects. -Serve as the primary contact to ensure appropriate communications, trial management, and adherence to timelines. -Coordinate the operational aspects of new and ongoing clinical trials at the site.

Requirements

• management
• interpersonal
• 2+ years
• clinical research
• high school
• medical

What You Bring

-Good management and organizational skills, with a strong understanding of medical procedures. -Exceptional interpersonal skills and the ability to work independently. -Minimum of 2 years of experience as a Clinical Research Coordinator. -At least a High School Diploma is required.

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Benefits

-Medical, dental & vision -Health Spending Account (HSA) -Short and long-term disability -Critical Illness, Accident, and Hospital -401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available -Employee Assistance Program -Life Insurance (Voluntary Life & AD&D for the employee and dependents) -Transportation benefits -Time Off/Leave (PTO, Vacation or Sick Leave)

About Actalent

-Born in July 2021 by merging Aerotek’s engineering & sciences arm with EASi, Actalent emerged as a focused engineering-and-science partner. -Backed by Allegis Group, it drives scale and speed to market via contract, managed, and technical services. -Headquartered in Maryland with global reach, it deploys specialized teams across North America, Europe, and APAC on Fortune 500 projects. -Typical engagements span EV design, vaccine development, lab services, clinical research, and infrastructure systems. -Expertise covers a wide spectrum: aerospace, defense, healthcare, manufacturing, software systems, environmental and civil engineering.

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