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Clinical Research Coordinator
Contract: Palo Alto, California, US
Salary Range: 45.00 - 51.00 | Per Hour
Job Code: 372066
End Date: 2026-10-31
Days Left: 23 days, 23 hours left
Client: University Research Centre
Job Title: Clinical Research Coordinator BMT
Location: Palo Alto, CA 94304 - Hybrid Role
Duration: 06 Months (Extension/Conversion based on performance)
Pay Range: ($45 - $51) on an hourly basis.
Overview
- Seeking a Clinical Research professional to independently manage clinical research activities, with a focus on oncology treatment trials and Phase I studies in Bone Marrow Trials (BMT).
- This healthcare setting role involves patient recruitment, study coordination, regulatory compliance, data management, and collaboration with Principal Investigators and study sponsors.
Required Qualifications:
- Bachelor's degree in a related field.
- 2+ years of clinical research experience.
- Direct experience with oncology treatment trials and Phase I studies.
- Experience working in an onsite healthcare/academic medical environment; CRO/Pharma CRA-only experience is not the target profile.
- Experience with EPIC and clinical research databases.
- Knowledge of FDA, IRB, HIPAA, and G CP requirements.
- Strong knowledge of clinical research protocols and medical terminology.
- Strong communication, organizational, and interpersonal skills.
- Proficiency in MS Office.
Key Responsibilities:
- Manage patient recruitment, enrollment, and retention for oncology clinical trials.
- Coordinate and support Phase I and oncology treatment studies from initiation through completion.
- Manage clinical research data, including collection, tracking, analysis, and reporting.
- Ensure compliance with IRB, FDA, HIPAA, and Good Clinical Practice (G CP) requirements.
- Prepare and maintain regulatory documentation and support IRB submissions and renewals.
- Monitor study activities, identify compliance issues, and implement corrective actions.
- Collaborate with Principal Investigators, sponsors, clinical teams, and research staff.
- Monitor and report serious adverse events and resolve study-related queries.
- Develop study timelines, milestones, budgets, and operational processes.
- Train and mentor research staff or students as assigned.
- Work with EPIC and other clinical/research databases to support study operations.
Benefits:
- The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable.
Job Requirement
- Oncology
- Bone Marrow
- Phase I
- Trials
- Research
- EPIC
Reach Out to a Recruiter
- Recruiter
- Phone
- Mradul Khampariya
- mradul.khampariya@collabera.com
Apply Now
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