Clinical Research Coordinator 2

Clinical Research Coordinator

Pay Rate Range: $35.00 - 38.10/hr (W2)

Employment Type: Contract

Duration: Through December 31, 2026 (with potential for extension or conversion)

Schedule: Full-Time, 40 hours/week, Monday-Friday, Day Shift

Location: Palo Alto, CA 94305 (100% Onsite)

Job Code: JPC-12440
Position Overview

Tekberry is seeking a Clinical Research Coordinator to support innovative oncology clinical research studies for one of our premier healthcare partners. This role will coordinate moderately complex clinical trials from study start-up through closeout, working closely with principal investigators, research staff, sponsors, and study participants to ensure successful execution of clinical protocols while maintaining regulatory compliance.

This is an excellent opportunity for a clinical research professional with experience in oncology treatment trials who enjoys working directly with patients and contributing to cutting-edge medical research.
Responsibilities

• Coordinate clinical research studies from initiation through study closeout.
• Serve as the primary point of contact for research participants, study sponsors, and regulatory agencies.
• Screen, recruit, consent, and enroll study participants according to approved protocols.
• Coordinate patient visits, procedures, specimen collection, and laboratory processing.
• Collect, manage, and maintain patient and study data using research databases and case report forms.
• Prepare and maintain study documentation, regulatory binders, and Institutional Review Board (IRB) submissions.
• Review research records for accuracy and protocol compliance.
• Assemble study materials and coordinate study visit logistics.
• Monitor study budgets, research expenditures, and billing activities.
• Participate in sponsor monitoring visits, regulatory audits, and research meetings.
• Collaborate closely with investigators to ensure patient safety and adherence to study protocols.

Required Qualifications

• Bachelor's degree in a related field, or equivalent combination of education and clinical research experience.
• 1-2 years of clinical research experience.
• Experience coordinating oncology clinical research studies.
• Experience supporting Phase I-III oncology treatment trials.
• Experience working as an onsite Clinical Research Coordinator within a healthcare or hospital environment.
• Strong knowledge of medical terminology.
• Proficiency with Microsoft Office.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple priorities while maintaining exceptional attention to detail.

Preferred Qualifications

• Experience with oncology treatment trials in an academic medical center.
• Clinical research certification through SOCRA or ACRP.
• Experience working directly with principal investigators, sponsors, and regulatory agencies.
• Knowledge of IRB processes, Good Clinical Practice (GCP), and FDA regulations.

Work Environment

• 100% onsite clinical research environment.
• Frequent interaction with patients, physicians, nurses, and research staff.
• Frequent standing, walking, bending, and computer work throughout the day.
• Must be able to lift up to 40 pounds occasionally.
• Opportunity for extension or conversion based on business needs and performance.

We need hard-working, reliable employees. If you're ready to contribute to meaningful clinical research while supporting innovative oncology studies, we'd love to hear from you.

As a Tekberry W2 employee, you will have access to health benefits, including medical, dental, and vision coverage, based on eligibility.

Tekberry is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Tekberry is a certified Minority Business Enterprise (MBE) and Disadvantaged Business Enterprise (DBE).

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