Onsite Clinical Research Coordinator — Part-Time, 20h/wk

SiteBridge Research; Walhalla (SC); On-site; USD 30,000 - 45,000; Part time

Job summary

SiteBridge Research in Walhalla, SC is seeking a part-time Clinical Research Coordinator responsible for supporting the Principal Investigator and managing clinical trial operations. You're expected to ensure compliance with regulations and oversee participant recruitment and data management.

The role requires a Bachelor’s degree in a relevant life science and a minimum of 3 years of clinical trial experience. This position demands strong problem-solving skills, attention to detail, and effective communication.

Qualifications

• Minimum 3 years of experience in clinical site/trials.
• Strong problem-solving skills and initiative.
• Excellent written and verbal communication skills.

Responsibilities

• Ensure adherence to study protocols and regulatory standards.
• Manage participant recruitment and scheduling for studies.
• Maintain research records and documentation for studies.

Skills

Detail-oriented

Interpersonal skills

Analytical mindset

Knowledge of FDA & ICH GCP regulations

Bilingual in English and Spanish

Proficient in MS Office

Education

Bachelor’s degree in relevant life science

Job description

SiteBridge Research in Walhalla, SC is seeking a part-time Clinical Research Coordinator responsible for supporting the Principal Investigator and managing clinical trial operations. You're expected to ensure compliance with regulations and oversee participant recruitment and data management.

The role requires a Bachelor’s degree in a relevant life science and a minimum of 3 years of clinical trial experience. This position demands strong problem-solving skills, attention to detail, and effective communication.