What are the responsibilities and job description for the Clinical Research Study Start Up Coordinator position at SQRL?
Highlights:
- Growing Company: Join a rapidly expanding team that is a recognized global leader in clinical trials for cognitive impairment.
- Hybrid Role: Flexible working with a combination of remote and in-office work based in Houston.
- Professional Development: Continuous learning opportunities and career growth.
- Comprehensive Benefits: Excellent health, dental, vision insurance, 401(k) with employer match, PTO, and more.
About the Role:
Our client is seeking a dedicated Clinical Trials Start-Up Coordinator to join their clinical trials team. This role involves managing the start-up process for clinical trials across all site locations in the US, ensuring compliance with ICH GCP guidelines and trial-specific protocols.
Key Responsibilities:
- Manage the clinical trials pipeline tracker and report on progress.
- Complete and submit site-specific feasibility and pre-qualification processes.
- Coordinate set-up activities and prepare essential documentation.
- Ensure preparation and amendments of site-specific Informed Consent Forms (ICF).
- Collaborate with third-party vendors, CROs, and sponsor representatives.
Requirements:
- Bachelor's degree in a science, technical, or health-related field.
- Minimum 1 year of experience in clinical research at site level.
- IT proficiency, HIPAA, and GCP trained.
- Excellent verbal and written communication skills.
- 6 months of experience in CNS trials is preferred
- Experience with electronic data capture systems, e.g., Medidata RAVE.
Benefits:
- 4 weeks PTO
- Health, dental, and vision insurance
- 401(k) retirement plan with employer match
- Life and disability insurance
- Health Savings Account
- Professional development assistance
Salary : $55,000 - $65,000
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