Clinical Research Coordinator (RN)

Research Services Inc

Sanford, FLFull-timePosted Apr 9, 2026

70K–80K a year

Behavioral Health Market Context

Apply Nowvia Indeed

Job Description

to ensure compliance with regulations and protocols.

What You Will Do:

- Coordinate and manage day-to-day trial activities from start to finish

- Complete screening and follow up visits as delegated by PI

- Obtain informed consent from participants and maintain accurate documentation following Good Clinical Practice guidelines

- Collect, document, and manage study data with accuracy and integrity

- Collaborate across multidisciplinary teams to ensure study success

What We Are Looking For:

- Must have a minimum of 2 years of experience as a CRC with industry sponsored clinical trials.

- Must have expertise with Phlebotomy, ECGs, and Vital Signs, and patient intake

- Strong organizational skills and attention to detail

- Ability to work independently

- Stable work history

We are looking for someone to grow with our organization in a dynamic role. Please submit a current resume for consideration. Professional references will be required for all candidates.

Job Type: Full-time

Pay: $70,000.00 - $80,000.00 per year

Work Location: In person

Qualifications

  • Must have a minimum of 2 years of experience as a CRC with industry sponsored clinical trials
  • Must have expertise with Phlebotomy, ECGs, and Vital Signs, and patient intake
  • Strong organizational skills and attention to detail
  • Ability to work independently
  • Stable work history
  • We are looking for someone to grow with our organization in a dynamic role

Benefits

  • Pay: $70,000.00 - $80,000.00 per year

Responsibilities

  • and play a critical role in the execution of cutting-edge clinical trials that truly make a difference
  • The ideal candidate will be responsible for overseeing clinical research trials and sponsored research projects to ensure compliance with regulations and protocols
  • Coordinate and manage day-to-day trial activities from start to finish
  • Complete screening and follow up visits as delegated by PI
  • Obtain informed consent from participants and maintain accurate documentation following Good Clinical Practice guidelines
  • Collect, document, and manage study data with accuracy and integrity
  • Collaborate across multidisciplinary teams to ensure study success


More Jobs