In-House CRA II: Site & TMF Support

Worldwide; Northern (KY); Hybrid; USD 50,000 - 99,000; Full time

Benefits offered by this job

Competitive benefits

Job summary

Worldwide Clinical Trials seeks an In-house Clinical Research Associate II to manage sites, ensure compliance with GCP/SOPs, and support the clinical trial team. You will assist with TMF/ISF maintenance, monitoring visits, and data quality checks.

Ideal candidates have a four-year science degree and at least two years of CNS/Neurology clinical research experience, with strong communication and organizational skills. Competitive benefits apply based on location.

Qualifications

• Four-year college degree in a science-related field required.
• At least two years of clinical research experience in CNS/Neurology preferred.
• Strong communication and documentation skills are essential.

Responsibilities

• Assist with site management tasks per GCP and SOPs.
• Support CTMs and field CRAs to ensure timely site deliverables.
• Maintain TMF, ISF, and QA checklists with accuracy.
• Provide mentorship to junior team members as needed.
• Communicate regularly with sites per monitoring plans.

Skills

Communication skills

Organizational skills

Interpersonal skills

Regulatory knowledge

Microsoft Office

IVRS / eCRF familiarity

Education

Four-year college degree in medical/biological/health sciences

Two years clinical research experience

Tools

EDC systems

Job description

Worldwide Clinical Trials seeks an In-house Clinical Research Associate II to manage sites, ensure compliance with GCP/SOPs, and support the clinical trial team. You will assist with TMF/ISF maintenance, monitoring visits, and data quality checks.

Ideal candidates have a four-year science degree and at least two years of CNS/Neurology clinical research experience, with strong communication and organizational skills. Competitive benefits apply based on location.