Specialist, Study Training Compliance & DOA Management
New
C
Care AccessClinical Research
Remote within the United StatesFull-TimeMiddle
Salary60,000 - 80,000 USD per year
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Job Details
- Experience
- 2 years
- Required Skills
- Microsoft OfficeCompliance
Requirements
- Bachelor’s degree in Life Sciences, Health Administration, or a related field preferred.
- Minimum of 2 years of experience in a Central Support or clinical research support role.
- Proven experience supporting onboarding, training compliance, and/or access coordination in a regulated research environment.
- Demonstrated ability to navigate and work within compliance-driven systems and support multi-trial documentation workflows.
- Proficiency in Microsoft Office applications (Excel, Word, Outlook, SharePoint).
- Strong organizational and tracking skills; detail-oriented.
- Ability to work both independently and as part of a collaborative team.
- Strong interpersonal and communication skills.
Responsibilities
- Track and monitor clinical staff training completion, including study-specific and mandatory compliance training.
- Support delegation processes during study start-up by verifying that training aligns with assigned roles.
- Ensure documentation of training is complete, current, and meets ICH-GCP, SOP, and sponsor requirements.
- Support DOA matrix setup and maintenance by confirming training completion and role assignments.
- Upload and maintain essential staff training records, certifications, and staff documents in the eISF and associated systems.
- Support internal audits, monitoring visits, and sponsor document requests.
- Collaborate with internal stakeholders to support study training and access coordination across study phases.
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