Clinical Research Associate
Experis · Bethesda, MD · 2 wk ago
On-siteAnalyst$40–$45/hrContract
Location: Bethesda, Maryland
Pay Range: $40 - $45/hr W2
About the role
As part of the Clinical Operations Department, you will support the research and development efforts of a leading organization in the clinical research industry. The ideal candidate will demonstrate strong organizational skills, excellent communication abilities, and a proactive approach.
Responsibilities
- Review and process essential regulatory documents received from clinical trial sites
- Request missing or additional documentation and respond to protocol or process-related inquiries
- Maintain and organize Trial Master Files (TMF) and centralized document systems
- Track regulatory documents and workflow in a centralized web-based system or database
- Ensure documents meet FDA, ICH GCP, and sponsor requirements for accuracy and completeness
Requirements
- 3–5 years of experience in a clinical research setting
- Experience with regulatory document review/collection and knowledge of FDA and ICH GCP guidelines
- Experience with eTMF systems (e.g., Veeva Vault) and system administration skills
- Experience with Trial Master Files and centralized tracking systems
- Bachelor’s degree required
Benefits
- Opportunity to work with a dynamic and innovative team in the clinical research field
- Engage in meaningful projects that contribute to advancing healthcare solutions
- Collaborative work environment that values diversity and inclusion
- Develop your professional skills and grow within a reputable organization
- Supportive management committed to your career development
- Medical and Prescription Drug Plans (upon completion of waiting period)
- Dental Plan
- Vision Plan
- Health Savings Account
- Health Flexible Spending Account
- Dependent Care Flexible Spending Account
- Supplemental Life Insurance
- Short Term and Long Term Disability Insurance
- Business Travel Insurance
- 401(k), Plus Match
- Weekly Pay