Site Director - Clinical Research

 

📍 Location: Escondido, CA  | 🏥 Site Name: AMCR  | 🕒 Full-Time  | 🧪 Clinical Research

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We’re seeking a Site Director to help us continue to grow our clinical research site located in Escondido, California. Reporting to the Director of Regional Operations (RDO), the Site Director (SD) oversees daily operations at the site to ensure participant safety, sponsor satisfaction, and high-quality data. This role drives financial targets, enrollment goals, and Key Performance Indicators (KPIs), while ensuring strict adherence to Good Clinical Practice (GCP), International Council of Harmonization (ICH), applicable regulatory requirements and Company and site level policies and procedures. This role requires strong leadership and communication skills to guide and mentor staff, provide strategic direction, manage resources, and foster a collaborative environment to achieve research objectives.

 

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in Escondido, CA (no capabilities for remote or hybrid work)
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

 

💼 What We Offer

• Competitive pay + annual performance incentives
• Medical, dental, and vision insurance
• 401(k) plan with company match
• Paid time off (PTO) and company holidays
• A mission-driven culture focused on advancing medicine and improving patient outcomes

 

🚀 Why Join Us?

You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.

Operational Leadership & Study Management:

• Manage site facilities, workflows, and Clinical Trial Management Systems (CTMS) to ensure premium experience for study participants, staff, and sponsors
• Monitor clinical study progress, review monitor reports, and create risk management/mitigation strategies during the full lifecycle of a study
• Ensure that all studies are conducted in compliance with all applicable regulations, GCP, ICH, policies, and procedures. This work is supported by the RDO, Therapeutic Area Leadership (TA Leadership) and Quality team, which provides SOPs, training, best practices, quality reviews, issue resolution and expertise to ensure high-quality trial execution and that the site remains audit-ready for customer or regulatory inspections
• Responsible for the lifecycle of all site regulatory documentation, from initial start-up through ongoing maintenance
• Provide operational support for protocol-related questions and ensure all staff are trained on study-specific requirements, in coordination with the principal investigator
• Oversee external site partners/vendors, including onboarding, training, and performance monitoring
• Ensure proper storage and handling of study specimens and investigational products
• Partner with Headlands’ Shared Services teams, including TA Leadership, Quality, Central Regulatory, Finance, Human Resources, Budgets and Contracts, Participant Recruitment, and Business Development, to drive site performance and operational execution
• Partner with the RDO to align and execute on strategies to support organic growth at the site
• Proactively communicate real estate, capacity, equipment, vendor, staffing, or training needs to the RDO/AD to ensure the site has the resources necessary to conduct ongoing and upcoming clinical trials
• Duties as assigned

People & Team Management:

• Manage the full employee lifecycle for all site personnel, including interviewing, hiring, onboarding, performance reviews, and disciplinary actions in partnership with the Human Resources Business Partner (HRBP)
• Provide coaching, mentoring, and development plans for all direct reports and ensure that all site staff have coaching, mentoring and development plans to maintain high morale, retention, and an engaged workforce
• Collaborate with the Medical Director office, RDO/AD, and HRBP, as applicable on investigator hiring, onboarding, training, development, performance management, and investigator development plans
• Proactively assess staffing needs and manage coverage to ensure study participant safety and data integrity
• Foster a collaborative and productive work environment that encourages continuous improvement
• Lead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers
• Manage local team to meet/exceed quality and performance metrics, report key performance indicators to leadership team
• Serve as a Culture Champion to support our mission and values

Financial Management:

• Own site-level financial performance by taking action to achieve revenue, expense, profitability, budget, and forecast targets
• Partner with Finance and the RDO/AD to create, manage, and update accurate site budgets and monthly forecasts

Participant Recruitment & Business Development:

• Responsible for driving recruitment strategies to meet or exceed monthly participant screening, randomization, and retention targets
• Develop and execute study-specific recruitment plans prior to study start, including hold lists, screening and enrollment monitoring, and plan adjustments as needed to meet enrollment goals, with the support of the Participant Recruitment team
• Develop and support strategies to develop the site’s participant database through local community engagement strategies, physician-practice outreach, participation in community events, and pre-screening events
• Serve as the primary point of contact between the site team and sponsors and Contract Research Organizations (CROs)
• Participate in study feasibility processes, providing accurate site-specific data to secure future trials
• Maintain current site information, including investigator Curriculum Vitae (CVs), site capabilities, equipment, vendor relationships, and operational constraints, to support accurate feasibility assessments and sponsor/CRO discussions
• Communicate changes in investigator staffing, site capabilities, operational capacity, or strategic priorities that may impact current or future study opportunities
• Drive the growth and development of the site by identifying areas for improvement and innovation while staying informed of industry advancements

 

REQUIREMENTS:

Education:

• Bachelor's degree in a scientific, health-related, or business administration field or equivalent experience
• Advanced degree desirable

Experience & Skills:

• 1–3 years of direct People Management experience (Preferred)
• 3+ years as a Primary Clinical Research Coordinator (Preferred)
• Demonstrate ability to motivate teams and lead planning/organization efforts
• Strong critical thinking and proactive problem-solving abilities
• Proficiency in Clinical Trial Management Systems and standard office software
• Excellent interpersonal, written, and oral communication skills
• Growth mindset and a commitment to continuous improvement
• Strong conflict resolution and mediation skills; ability to manage and resolve disputes effectively
• Strong ethical standards and professionalism

 

Supervision:

• Responsible for the direct supervision of various levels of clinical research staff

Headlands Behavioral Characteristics:

• Solution-Oriented
• Adaptable
• Curious
• Insightful
• Collaborative
• Proactive
• Communicative