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Oncore Jobs in California (NOW HIRING)

Tekberry

Clinical Research Coordinator

Palo Alto, CA · On-site

$35 - $70/hr

Experience with Stanford systems (REDCap, eProtocol, OnCore, SeRA). * Knowledge of IRB processes, budget management, and sponsor interaction . * Demonstrated success in coordinating multi-site or ...

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Oncore information

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$371.8K

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How much do oncore jobs pay per year?

As of Aug 22, 2026, the average yearly pay for oncore in California is $371,816.00, according to ZipRecruiter salary data. Most workers in this role earn between $366,100.00 and $394,800.00 per year, depending on experience, location, and employer.

What is an Oncore?

An Oncore job typically refers to a position within the Oncore platform, a workforce management system used for contingent labor and project-based work. These jobs can vary across industries and may include contract, temporary, or gig-based roles. Oncore helps businesses efficiently manage and pay their contingent workforce while ensuring compliance with labor regulations. If you are hired for an Oncore job, you may work as an independent contractor or temporary employee depending on the arrangement.

What does an Oncore Clinical Research Associate do?

A typical day for an Oncore Clinical Research Associate involves monitoring ongoing clinical trials, ensuring they are conducted according to protocol, and reviewing data for accuracy and compliance. You'll frequently interact with study site staff, coordinate with investigators, and document findings in clinical trial management systems like OnCore. The role may also include onsite visits, remote monitoring, and regular meetings with sponsors or regulatory teams. Timely communication and attention to protocol details are crucial, making it a dynamic and collaborative work environment with opportunities to learn and grow within the clinical research field.

What are the key skills and qualifications needed to thrive in the Oncore position?

To thrive in an Oncore Clinical Research Associate role, a background in life sciences, clinical trial monitoring experience, and knowledge of regulatory guidelines such as GCP are essential. Proficiency in electronic data capture (EDC) systems, trial management software, and certifications like ACRP or SOCRA are often required. Excellent organizational skills, attention to detail, and effective communication help candidates excel in multi-site coordination and team settings. These capabilities ensure the smooth execution, compliance, and high-quality outcomes of clinical research studies.

What are popular job titles related to Oncore jobs in California?

For Oncore jobs in California, the most frequently searched job titles are:

What job categories do people searching Oncore jobs in California look for?

The top searched job categories for Oncore jobs in California are:

Oncore jobs near you
Infographic showing various Oncore job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $371,816 per year, or $178.8 per hour.

Clinical Research Coordinator

Tekberry

Palo Alto, CA • On-site

$35 - $70/hr

Other

Medical, Dental, Vision

Re-posted 20 days ago

Job description

Title: Clinical Research Coordinator
Pay Rate Range: $35.00 - $70.00/hr (DOE, based on experience and level)
Employment Type: Contract
Schedule: Full-time, Monday - Friday | 8:00 AM - 5:00 PM
Location: Stanford, CA 94305
Tekberry is looking for a highly organized and motivated Clinical Research Coordinator to work onsite with our client. In this role, you will support the coordination of oncology and other clinical trials within affiliated research divisions. The CRC will collaborate closely with investigators, sponsors, and study participants to ensure research activities are conducted safely, efficiently, and in compliance with federal, institutional, and sponsor requirements.
As a W2 employee, you will have access to health benefits including medical, dental, and vision coverage.
Responsibilities
Study Coordination and Participant Management (50%)
  • Serve as the primary contact for study participants, sponsors, monitors, and regulatory agencies.
  • Coordinate all phases of assigned studies-from start-up through close-out.
  • Screen, consent, and enroll participants according to protocol and IRB requirements.
  • Schedule and monitor study visits, collect biospecimens, and ensure timely and accurate data entry.
  • Maintain patient safety and ensure proper documentation of adverse events and deviations.

Regulatory and Compliance Oversight (30%)
  • Prepare, submit, and maintain all IRB and regulatory documents.
  • Ensure study compliance with GCP, FDA, and Stanford institutional policies.
  • Audit and review case report forms and source documentation for accuracy.
  • Support monitoring visits and respond to findings or corrective-action requests.
  • Maintain essential regulatory binders, correspondence, and approvals.

Financial and Administrative Support (20%)
  • Track study budgets, expenditures, and billing compliance.
  • Coordinate with finance and management teams to resolve discrepancies.
  • Assemble study kits, prepare materials for sponsor visits, and manage study logistics.
  • Support recruitment efforts and assist in developing patient outreach strategies.
Must-Have Qualifications
  • Bachelor's degree (minimum) in a science or health-related field; Master's preferred.
  • 2+ years of clinical research experience in an academic, hospital, or clinical-trial setting.
  • Familiarity with oncology, treatment trials, or NIH-funded research highly preferred.
  • Working knowledge of Good Clinical Practice (GCP), informed consent, and research ethics.
  • Proficiency with Microsoft Office, REDCap, and EHR systems such as EPIC.
  • Excellent communication, organization, and documentation skills.
  • Ability to work independently and manage multiple studies simultaneously.
Preferred Qualifications
  • Certification through SOCRA or ACRP.
  • Experience with Stanford systems (REDCap, eProtocol, OnCore, SeRA).
  • Knowledge of IRB processes, budget management, and sponsor interaction.
  • Demonstrated success in coordinating multi-site or industry-sponsored trials.
Work Environment
  • 100% onsite at Stanford University (some divisions may allow limited hybrid flexibility).
  • May be exposed to biological samples, chemicals, and clinical environments.
  • Occasional evening or weekend hours may be required for study visits or participant needs.
  • Must comply with all safety and infection-control policies.

Tekberry offers a $100 referral bonus for referrals resulting in successful placements!
Tekberry, Inc. is an equal opportunity employer. Qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected categories under applicable laws.
Tekberry, Inc. is a Certified Minority Business Enterprise (MBE) and Certified Disadvantaged Business Enterprise (DBE).
By submitting your resume, you consent to receive communications from our organization via text message. All texts are sent by real people, and we look forward to connecting with you about this opportunity!
Check out all our jobs at: https://tekberry.com/search-jobs/
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