Internal Clinical Research Associate
New
United StatesFull-TimeEntry
Salary72,500 - 157,200 USD per year
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Job Details
- Experience
- 0+ years of experience
- Required Skills
- GCP
Requirements
- Bachelor’s degree in Life Sciences or a related scientific discipline.
- 0+ years of experience.
- Experience in clinical research, clinical trial operations, or clinical study administration (preferred).
- Experience working under Good Clinical Practice (GCP) guidelines (preferred).
- Experience using electronic clinical trial databases, clinical trial management systems, or related research platforms (preferred).
- Experience supporting clinical trial audits, inspections, or regulatory submissions (preferred).
- Experience with clinical trial registration platforms and study reporting activities (preferred).
Responsibilities
- Support site identification, qualification, activation, monitoring, and closeout activities across clinical studies.
- Maintain Trial Master Files and essential study documents to ensure inspection readiness and regulatory compliance.
- Partner with clinical study teams to develop, review, and manage study documentation required for trial execution.
- Review and maintain informed consent forms, case report forms, and other study-related materials.
- Generate study newsletters and communications to support investigator sites and cross-functional stakeholders.
- Track and support study invoicing activities and maintain associated documentation.
- Create and maintain study metrics, reports, and dashboards to support clinical trial oversight and execution.
- Support clinical trial registration, audit preparation, data collection activities, and adherence to regulatory and Good Clinical Practice requirements.
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