Clinical Research Coordinator

Fides Clinical Research

Sandy Springs, GAFull-timePosted Apr 4, 2026

28 an hour

Behavioral Health Market Context

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Job Description

to Good Clinical Practice (GCP), FDA regulations, and other relevant standards
- Collect and record data accurately, including vital signs and blood sampling
- Review and maintain documentation for clinical trials
- Collaborate with healthcare professionals to ensure study protocols are followed
- Monitor participant safety and well-being throughout the study
- Assist in the preparation of study protocols and informed consent forms

Requirements:

- Bachelor's degree in a related field (preferred)
- Proven experience in clinical research or a healthcare setting
- Knowledge of HIPAA regulations and ethical principles in clinical research
- Familiarity with clinical development processes and procedures
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal abilities
- Ability to work effectively in a team environment

If you are passionate about contributing to the advancement of medical research and possess the required qualifications, we encourage you to apply for this rewarding opportunity as a Clinical Research Coordinator.

Job Type: Full-time

Pay: From $28.00 per hour

Ability to Commute:
• Sandy Springs, GA (Required)

Ability to Relocate:
• Sandy Springs, GA: Relocate before starting work (Required)

Work Location: In person

Qualifications

  • Proven experience in clinical research or a healthcare setting
  • Knowledge of HIPAA regulations and ethical principles in clinical research
  • Familiarity with clinical development processes and procedures
  • Strong attention to detail and organizational skills
  • Excellent communication and interpersonal abilities
  • Ability to work effectively in a team environment
  • If you are passionate about contributing to the advancement of medical research and possess the required qualifications, we encourage you to apply for this rewarding opportunity as a Clinical Research Coordinator
  • Sandy Springs, GA (Required)
  • Sandy Springs, GA: Relocate before starting work (Required)

Benefits

  • Pay: From $28.00 per hour

Responsibilities

  • The ideal candidate will play a crucial role in facilitating clinical research studies, ensuring compliance with regulatory standards and overseeing various aspects of the research process
  • Coordinate and oversee clinical research studies from initiation to completion
  • Ensure adherence to Good Clinical Practice (GCP), FDA regulations, and other relevant standards
  • Collect and record data accurately, including vital signs and blood sampling
  • Review and maintain documentation for clinical trials
  • Collaborate with healthcare professionals to ensure study protocols are followed
  • Monitor participant safety and well-being throughout the study
  • Assist in the preparation of study protocols and informed consent forms


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