ZipRecruiter

Log In

1

Director Clinical Research Operations Jobs (NOW HIRING)

OneOncology

Clinical Research Director

Charlotte, NC · On-site

Operations Manager FLSA Status: Exempt Department: Clinical Research Location: Carolina Oncology Specialist Pineville Location JOB SUMMARY: The Clinical Research Director is responsible for the ...

OneOncology

Clinical Research Director

Charlotte, NC

Operations Manager FLSA Status: Exempt Department: Clinical Research Location: Carolina Oncology ... The Director provides leadership to research staff, oversees study portfolios, manages sponsor and ...

Southwest Women's Oncology

Be Seen First

Clinical Research Director

Albuquerque, NM · On-site

Clinical Research Director Southwest Women's Oncology | Albuquerque, New Mexico Why This Role ... Trial Operations * Lead the full lifecycle of clinical trials--feasibility, start-up, recruitment ...

NS Pharma Inc

Director, Clinical Research

Paramus, NJ · On-site

$210K - $240K/yr

... global clinical studies. * Direct and manage the performance of study vendors (e.g., CROs and ... Accountable for the creation of study related documentation (protocol, ICF, CRF, operations manuals ...

next page

Showing results 1-20

All JobsDirector Clinical Research Operations Jobs

Director Clinical Research Operations information

See salary details

$60K

$146K

$282.5K

How much do director clinical research operations jobs pay per year?

As of Jun 16, 2026, the average yearly pay for director clinical research operations in the United States is $145,969.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,000.00 and $173,500.00 per year, depending on experience, location, and employer.

What is the difference between Director Clinical Research Operations vs Clinical Research Manager?

AspectDirector Clinical Research OperationsClinical Research Manager
ResponsibilitiesOversees multiple clinical projects, strategic planning, and department leadershipManages daily clinical trial activities, site coordination, and team supervision
Required CredentialsBachelor's/Master's in life sciences, extensive experience, often certificationsBachelor's degree, relevant experience, certifications preferred
Work EnvironmentSenior leadership in pharmaceutical or biotech companiesOperational teams within clinical research sites or CROs
Industry UsageUsed in large organizations for strategic rolesCommon in mid-sized to large research organizations

The main difference is that the Director Clinical Research Operations focuses on strategic oversight and leadership of clinical research activities, while the Clinical Research Manager handles day-to-day trial management and site coordination. Both roles require relevant experience and certifications, but the director position involves broader organizational responsibilities.

What does a Director of Clinical Research Operations do?

A Director of Clinical Research Operations oversees the planning, execution, and management of clinical research studies within an organization. They are responsible for ensuring compliance with regulatory requirements, managing budgets and timelines, and leading teams of clinical research professionals. Their role includes collaborating with cross-functional departments, optimizing operational efficiency, and maintaining high standards of data quality and patient safety throughout the clinical trial process.

What are some common challenges faced by a Director of Clinical Research Operations, and how can they be effectively managed?

A Director of Clinical Research Operations often faces challenges such as balancing regulatory compliance with operational efficiency, managing cross-functional teams, and ensuring timely study delivery within budget constraints. To address these, it’s important to establish robust communication channels, develop standardized processes, and foster a collaborative environment with clinical staff, regulatory affairs, and sponsors. Staying updated on evolving regulations and investing in team training also help in proactively managing these complexities, ensuring both compliance and successful study outcomes.

What are the key skills and qualifications needed to thrive as a Director of Clinical Research Operations, and why are they important?

To thrive as a Director of Clinical Research Operations, you need extensive knowledge of clinical trial management, regulatory compliance, and a background in life sciences or a related field, often supported by an advanced degree and significant industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as CCRA or CCRP are typically required. Strong leadership, strategic planning, and interpersonal skills distinguish top performers in this role. These skills ensure effective oversight of complex research projects, regulatory adherence, and successful collaboration across multidisciplinary teams.
More about Director Clinical Research Operations jobs
What cities are hiring for Director Clinical Research Operations jobs? Cities with the most Director Clinical Research Operations job openings:
What are the most commonly searched types of Clinical Research Operations jobs? The most popular types of Clinical Research Operations jobs are:
What job categories do people searching Director Clinical Research Operations jobs look for? The top searched job categories for Director Clinical Research Operations jobs are:
Director Clinical Research Operations jobs near you
Infographic showing various Director Clinical Research Operations job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 59% Full Time, 23% Part Time, 1% Temporary, and 12% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $145,969 per year, or $70.2 per hour.
Clinical Research Operations Specialist

Clinical Research Operations Specialist

Loma Linda University Health

Loma Linda, CA

Other

Posted 16 hours ago

Loma Linda University Health rating

8.1

Company rating: 8.1 out of 10

Based on 86 frontline employees who took The Breakroom Quiz

109th of 999 rated hospitals

Job description

MC: Cancer Institute Core- Temporary- Full-Time, Day Shift

Job Summary: The Clinical Research Operations Specialist for the Cancer Center Clinical Trials Unit (CCCTU) plays a critical role in the financial management of clinical research trials from study startup to study closure.  The Clinical Research Operations Specialist participates in the start-up activities related to opening new trials, including performing financial feasibility assessments, and will work closely with the Principal Investigator, study start-up team and Research Affairs Financial Management to ensure accurate and compliant budget development and negotiation.   Develops the Medicare Coverage Analysis to begin budget development. Creates new studies in the OnCore Clinical Trial Management System and tract contract milestones and EPIC to support charge review and research billing compliance.  The Clinical Research Operations Specialist develops and negotiates budgets for clinical trials working with sponsors, ancillary departments, and billing offices.  This position requires the ability to interpret study protocols, identify billable vs research-only procedures and ensure alignment between clinical activities and financial workflows.  Facilitates and processes financial transactions for clinical trial accounts.   Performs other duties as needed. 

Education and Experience: Bachelor's Degree in Healthcare Administration, Finance, or account required.   Minimum two years experience in clinical research finance, budget development or contract negotiation required.  Experience with oncology clinical trials at an academic medical center or cancer research institution preferred.    

Knowledge and Skills: Knowledge of clinical trial practices, billing compliance regulation, Medical coverage analysis, and medical terminology.   Familiarity with budgeting for cell therapy studies. Experience with early phase or complex trial designs.  Knowledge of fair market value standards and budgeting practices for high-cost research procedures.  Working knowledge of CPT codes, RVUs, and Medicare billing practices in clinical research.  Read, write legibly, and speak in English with professional quality; use computer, printer, and software programs necessary to the position (e.g., Word, Excel, Outlook, PowerPoint). Operate/troubleshoot basic office equipment required for the position.  Relate and communicate positively, effectively, and professionally with others; work calmly and respond courteously when under pressure; collaborate and accept direction.  Think critically; manage multiple assignments effectively; organize and prioritize workload; work well under pressure; problem solve; recall information with accuracy; pay close attention to detail; work independently with minimal supervision.  Distinguish colors as necessary; hear sufficiently for general conversation in person and on the telephone, and identify and distinguish various sounds associated with the workplace; see adequately to read computer screens, and written documents necessary to the position.

Licensures and Certifications: None.

Our mission is to continue the teaching and healing ministry of Jesus Christ. Our core values are compassion, excellence, humility, integrity, justice, teamwork and wholeness.
Loma Linda University Health is a Seventh-day Adventist, faith and values based Christian institution. Candidates must understand and embrace the mission, purpose, and identity of Loma Linda and its affiliated entities.

We are an equal opportunity employer committed to the principles of diversity. We provide equal opportunities in all aspects of the employment process to every individual, regardless of gender, race, color, age, national origin, ancestry, physical or mental disability, marital or veteran status, genetic information or any other characteristic protected by law. In addition, we will provide reasonable accommodations for otherwise qualified individuals requesting an accommodation due to a disability. If you need accommodation assistance with accessing our job listings or completing an application, or during any other phase of employment with us, please contact Human Resources Management at (909) 651-4001.

Loma Linda University Medical Center is a religiously-qualified Equal Opportunity Employer under Title VII of Civil Rights Act of 1964. No question on this application is asked for the purpose of unlawfully limiting or excluding any applicant's consideration for employment because of race, color, religion, gender, age, national origin, disability, genetic information, or any other status protected by applicable law. If you need a reasonable accommodation in the hiring process, please notify Human Resource Management.

We appreciate your interest in Loma Linda and wish you success in your job search!

What Loma Linda University Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Loma Linda University Health logo

About Loma Linda University Health

Sourced by ZipRecruiter

Loma Linda University Health (LLUH) is an esteemed healthcare organization situated in Loma Linda, California, US. Established in 1905, it was initially known as the College of Medical Evangelists, and it operated as the official medical institution of the Seventh-day Adventist Church until the name was changed to LLUH in 1961. LLUH is very much active in the healthcare and education sectors, providing a vast range of services such as medical treatment, research, and health education. The organization’s core mission is "to continue the teaching and healing ministry of Jesus Christ", which underlines its binding values of compassion, integrity, excellence, freedom, and justice.

Industry

Health care and social assistance and hospitality services

Company size

10,000+ Employees

Headquarters location

Loma Linda, CA, US

View All Loma Linda University Health Jobs

Apply