Clinical Research Coordinator II - Study & Compliance

SGS; Richardson (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

SGS is seeking a dedicated professional to coordinate and facilitate clinical studies in Richardson, Texas. The position involves ensuring compliance with clinical protocols and regulations, maintaining detailed documentation, and training new staff.

The ideal candidate will have a Bachelor’s degree in science and at least 2 years of relevant experience in clinical research. A strong understanding of Good Clinical Practices (GCP) is crucial, and certification (CCRC/CCRA) is a significant advantage.

Qualifications

• 2+ years relevant work experience in clinical research.
• Basic understanding of Good Clinical Practices (GCP).
• CCRC/CCRA certification is a strong plus.

Responsibilities

• Coordinate daily activities of clinical studies according to protocols.
• Prepare and maintain study documentation forms.
• Train and mentor new clinic staff.

Skills

Clinical research knowledge

Training and mentoring

Documentation management

Education

Bachelor’s degree in science or equivalent

Job description

SGS is seeking a dedicated professional to coordinate and facilitate clinical studies in Richardson, Texas. The position involves ensuring compliance with clinical protocols and regulations, maintaining detailed documentation, and training new staff.

The ideal candidate will have a Bachelor’s degree in science and at least 2 years of relevant experience in clinical research. A strong understanding of Good Clinical Practices (GCP) is crucial, and certification (CCRC/CCRA) is a significant advantage.