Site Director

Flourish Research•San Diego, CA

2d•Onsite

About The Position

Valkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! We are actively hiring a Site Director to support our Valkyrie Clinical Trials San Diego, CA site.

Requirements

Bachelor’s degree in Life Sciences, Healthcare, Nursing, or related field; advanced degree strongly preferred.
8–12+ years of clinical research experience, with at least 5 years in site operational leadership.
Direct oncology research experience required, minimum 2+ years.
Demonstrated success managing P&L, large teams, and complex clinical operations.
Strong communication, leadership, conflict management, and process improvement skills.
Exceptional knowledge of clinical research methods.
Excellent oral and written communication skills.
Excellent computer skills to include Office365 products.
Experience in writing and reviewing Standard Operating Procedures.
Strong problem solving, risk assessment and impact analysis abilities.
Demonstrated experience in process improvement.
Strong negotiation and conflict management skills.
Flexible and able to multi-task and prioritize competing demands.
Ability to think independently and influence when appropriate.

Nice To Haves

Advanced degree

Responsibilities

Oversee day-to-day oncology site operations, ensuring compliance with FDA, ICH-GCP, and sponsor protocols.
Implement and monitor operational and financial metrics including study volume, capacity planning, margins, and productivity.
Lead development, execution, and continuous improvement of SOPs aligned with Flourish Research and oncology-specific requirements.
Ensure high-quality study conduct, patient safety oversight, and robust PI/Sub-I engagement.
Partner with Quality and Risk to achieve strong audit outcomes and uphold data integrity.
Own the oncology site P&L; manage to margin/EBITDA targets.
Develop and implement growth strategies to expand study volume, diversify oncology indications, and strengthen site competitiveness.
Partner with Business Development to maintain sponsor relationships and attract new studies.
Support financial budgeting, forecasting, and resource planning.
Leverage oncology market trends and sponsor pipelines to shape site strategy.
Strengthen partnerships with oncology practices, referral networks, and community physicians.
Contributes competitive positioning within the oncology site network landscape.
Recruit, mentor, and develop clinical and operational staff with oncology expertise.
Champion patient-centered, mission-driven culture aligned with Flourish core values.
Collaborate closely with investigators and medical leadership to support high-acuity oncology trials.
Implement and optimize clinical systems, CTMS platforms, and workflow automation.
Support integration across HR, IT, Quality, and Finance when applicable.
Standardize processes and performance dashboards to drive operational excellence.
Maintain site-level adherence to GCP, ICH, FDA regulations, HIPAA, and oncology-specific safety requirements.
Oversee staff competency, training, and readiness for audits and monitoring visits.