Clinical Research Coordinator II

Tekberry is seeking an experienced Clinical Research Coordinator II to support oncology clinical trials within the Stanford School of Medicine. This role is designed for a seasoned onsite clinical research coordinator who can independently manage complex research activities particularly treatment-based and Phase I oncology trials.

The Clinical Research Coordinator II will play a critical role in study execution regulatory compliance data integrity and collaboration with Principal Investigators and sponsors. As a Tekberry W2 employee you will have access to health benefits including medical dental vision and 401(k) options.

• Independently manage significant aspects of large clinical studies or oversee all aspects of one or more smaller studies.

• Lead subject recruitment and enrollment efforts; develop and implement effective participant recruitment and retention strategies.

• Oversee data management activities including developing systems for data collection monitoring reporting and analysis.

• Extract analyze and interpret clinical research data.

• Develop project schedules targets metrics and accountability plans.

• Lead team meetings and prepare or approve meeting documentation.

• Supervise train and mentor junior staff or students as assigned.

• Audit study operations to ensure compliance with protocols GCP IRB HIPAA FDA and institutional regulations.

• Monitor and manage IRB submissions renewals and regulatory correspondence.

• Collaborate closely with Principal Investigators and sponsors.

• Monitor document and report serious adverse events; resolve study queries.

• Develop and manage study budgets including identifying standard-of-care vs. study-related procedures.

• Track study milestones and support sponsor invoicing per study contracts.

• Ensure ongoing regulatory compliance through routine review of study documentation.

• Support Investigational New Drug (IND) submissions to the FDA when applicable.

• Bachelors degree required.

• 2 years of onsite clinical research coordinator experience (site-side experience only).

• Oncology clinical trials experience required.

• Experience supporting treatment-based and Phase I clinical trials.

• Strong knowledge of research regulations including GCP HIPAA FDA and IRB requirements.

• Proficiency with Microsoft Office and research databases.

• Strong organizational communication and interpersonal skills.

• Ability to work independently and manage complex study requirements.

• SOCRA or ACRP certification.

• Experience in academic medical center or hospital-based research settings.

• Strong understanding of medical terminology.

• 100% onsite role.

• Clinical and research environment with potential exposure to hazardous materials blood or biological specimens.

• May require flexible or extended hours based on research needs.

• Will not be working with minors.

• Driving not required for this role.

We need hard-working reliable employees. Tekberry offers a $100 referral bonus for referrals that result 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 category under applicable laws.

Tekberry Inc. is a Certified Minority Business Enterprise (MBE) and Certified Disadvantaged Business Enterprise (DBE).

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