Clinical Trial Coordinator
L
LifelancerClinical research
Source API remote eligibility restrictions: United StatesFull-TimeJunior
Salary not disclosed
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Job Details
- Languages
- Good English language and grammar skills
- Experience
- 2+ years’ experience in global clinical trial support as a CTC / CTC / Project Coordinator
- Required Skills
- MS Office
Requirements
- Bachelor's degree preferred.
- Have 2+ years’ experience in global clinical trial support as a CTC or Project Coordinator.
- Have experience with Veeva Vault and hands-on experience with the eTMF life cycle.
- Have good English language and grammar skills.
- Be proficient in MS Office, including Word, Excel, and PowerPoint.
- Maintain working knowledge of applicable country regulations, ICH Good Clinical Practices, and organization/client SOPs and WPDs.
- Be able to analyze project-specific data and systems for accuracy and efficiency.
- Demonstrate organizational skills, attention to detail, and the ability to handle multiple tasks.
- Be able to work independently or as part of a team and reprioritize work as project timelines change.
- Complete the organization's clinical training program.
Responsibilities
- Provide support for day-to-day clinical study activities under the FSP Manager’s supervision and in collaboration with Client Management.
- Collaborate with Clinical Operations/Study Managers, study teams, and CROs to support study activities.
- Review essential document packets, study plans, informed consent forms, and other study documentation.
- Support and oversee risk-based monitoring.
- Attend key team meetings and prepare minutes for selected studies.
- Support regulatory inspection readiness, including SOP lists and storyboard collation.
- Support CTMS/TMF activities and vendor contract administration as required.
- Support site activation activities and study close-out, including financial reconciliation.
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