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Collabera

Clinical Research Coordinator

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Job Description

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.

Benefits

  • Paid Time Off (PTO)
  • Sick Leave
  • 401(k) Plans
  • Other Retirement and Savings