Hire the right healthcare staff with speed and precision locally or nationwide.

Learn More

How to Cost-Effectively Build a Nursing Staff in an Age of Travel Nursing

Uncover alternative and sustainable staffing solutions to address nursing shortages

Read the article

Life Sciences

Hire skilled life sciences talent by partnering with a nationwide recruitment agency with local market expertise.

Current Trends in the Life Sciences Job Market

Learn how partnering with a staffing agency is a powerful way to combat the challenges of hiring in the current life sciences job market

Read the article


Execute critical healthcare IT initiatives with increased flexibility and cost-effectiveness with us at your side.

The Technology Hiring Outlook: What We're Seeing Right Now

Uncover how to handle an employee-led technology market.

read the article

For JobSeekers

Match your unique skills with in-demand jobs at growing organizations.

Learn More

Resource Center

Explore our library of insights and tips designed to help healthcare leaders and job candidates align.

Explore resources

About Us

We’re positively impacting lives as a leading provider of workforce solutions for clients and talent.

Learn More

Back to jobs

Clinical research coordinator

Posted: June 27, 2024
Salary:US$28.00 - US$35.00 per hour
Job type: Permanent
Discipline:Life Sciences
Work Location:On-site

Job description

We are looking to add a CRC to our growing team- if you enjoy a collaborative environment and are looking for a company with a ton of room for growth- join our team! We are looking for someone interested in moving into a leadership role in the next 12 months.

Qualified candidates will have at least 3-4 years of experience working in therapeutic or medical device clinical trials.

Responsibilities include:

  • Maintaining thorough knowledge of study-specific inclusion/exclusion criteria
  • Performing safety and efficacy assessments per protocol
  • Vital signs, EKGs, and other assessments as assigned
  • Accurate and timely completion of source documents recording participant's participation in the study
  • Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines
  • Assist investigators in the collection of information from participants regarding AEs, concomitant medications, and other changes throughout participation
  • Responsible for timely data entry and query resolution
  • Timely reporting of study events (SAEs, protocol deviations, etc.)
  • Following subjects through study completion and creating a follow-up care plan with a physician, study subject, and primary care provider;
  • Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters
  • Prompt and professional communication with sponsors, representatives, and other study-related parties
  • Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors, and all other study-related personnel, and staff members
  • Interacting with nursing/unit staff on a daily basis as applicable to ensure communication and accurate completion of source through daily chart review
  • Keeping CTM informed of study status and any study-related issues
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials