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Clinical Research Operations Jobs (NOW HIRING)

Ohio State University

Manager- CCRM Clinical Research Operations Department:Medicine | Center for Clinical Research Management Serves as Clinical Research Manager in the College of Medicine (COM) Center for Clinical ...

Andvaris Inc

Clinical Operations Manager

Miami, FL · On-site

🔹 Operations Manager - Clinical Trials 🔹 A premier healthcare organization in South Florida ... This is an excellent opportunity for a seasoned clinical research professional to make an immediate ...

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Clinical Research Operations information

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$49K

$107.3K

$189K

How much do clinical research operations jobs pay per year?

As of Jun 15, 2026, the average yearly pay for clinical research operations in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an intermediate or experienced role that requires prior knowledge of clinical trial processes, good clinical practice (GCP), and often some related experience. Entry-level positions in clinical research may be labeled as Clinical Trial Assistants or Coordinators, with CRAs usually needing a bachelor's degree and relevant training or certifications before advancing to this role.

What is the difference between Clinical Research Operations vs Clinical Research Coordinators?

AspectClinical Research OperationsClinical Research Coordinators
CredentialsTypically requires a degree in life sciences, certifications like CCRP or RACOften requires a bachelor's degree in health sciences or related field, with certifications like CCRP beneficial
Work EnvironmentOversees multiple studies, manages teams, and collaborates with sponsors and regulatory bodiesWorks directly with study participants, manages data collection, and ensures protocol adherence
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutionsCommonly employed in hospitals, clinics, and research sites

Clinical Research Operations professionals focus on managing entire research programs, budgets, and teams, while Clinical Research Coordinators handle day-to-day study activities and participant interactions. Both roles are essential but differ in scope and responsibilities within the clinical research field.

What are some common challenges faced in clinical research operations and how can they be addressed?

Professionals in clinical research operations often encounter challenges such as managing complex regulatory requirements, coordinating across multidisciplinary teams, and ensuring adherence to strict timelines. Successfully addressing these challenges typically involves strong project management skills, effective communication with stakeholders, and staying updated on regulatory changes. Leveraging technology for data management and fostering a collaborative work environment can also help streamline processes and improve trial outcomes.

Which is better, CRC or CRA?

Clinical Research Coordinators (CRCs) and Clinical Research Associates (CRAs) have different roles in clinical trials; CRCs typically manage study conduct at sites, while CRAs monitor trial progress across multiple sites. Both roles require strong organizational skills and knowledge of Good Clinical Practice (GCP), but CRAs often need more experience in monitoring and may travel frequently. The choice depends on your career interests, as CRCs focus on site management and patient interaction, whereas CRAs focus on oversight and compliance.

What is clinical research operations?

Clinical research operations refer to the planning, execution, and management of clinical trials and studies that test new medical treatments, drugs, or devices. This field ensures that studies are conducted ethically, efficiently, and in compliance with regulatory guidelines. Professionals in clinical research operations coordinate activities such as patient recruitment, data collection, regulatory submissions, and quality control. Their work is essential for advancing medical knowledge and ensuring the safety and effectiveness of new healthcare interventions.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the complexity of trials managed. Salaries can vary based on the employer, clinical setting, and additional skills such as data management or regulatory knowledge.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant experience, a degree in life sciences or related fields, and knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles may be available for those with strong academic backgrounds or internships, but advancing typically involves gaining experience and certifications such as the CCRP or RAC. The job market varies based on industry demand and geographic location.

What are the key skills and qualifications needed to thrive in Clinical Research Operations, and why are they important?

To thrive in Clinical Research Operations, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as ICH-GCP), and project management, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are often required. Exceptional organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring compliance. These competencies are vital for maintaining data integrity, meeting regulatory standards, and successfully managing complex clinical studies.
More about Clinical Research Operations jobs
What cities are hiring for Clinical Research Operations jobs? Cities with the most 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 states have the most Clinical Research Operations jobs? States with the most job openings for Clinical Research Operations jobs include:
What job categories do people searching Clinical Research Operations jobs look for? The top searched job categories for Clinical Research Operations jobs are:
Clinical Research Operations jobs near you
Infographic showing various Clinical Research Operations job openings in the United States as of June 2026, with employment types broken down into 4% As Needed, 87% Full Time, 7% Part Time, 1% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Director Clinical Research Operations

Director Clinical Research Operations

Arkansas Children's

Little Rock, AR • On-site

Full-time

Posted 3 days ago

Arkansas Children's Hospital rating

7.4

Company rating: 7.4 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

318th of 999 rated hospitals

Job description

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS.
This position has been designated as safety sensitive and cannot be filled by a candidate who is a current user of medical marijuana.
CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account (https://www.myworkday.com/archildrens/)and search the "Find Jobs" report.
Work Shift:
Please see job description for details.
Time Type:
Full time
Department:
CC033020 Clinical Research Operations
Summary:
Develops, oversees, and ensures strategic growth of a large, multidisciplinary clinical research organization which includes operational clinical research services (feasibility, study start-up, budget development and negotiation, regulatory, clinical research coordination, research nursing support, invoicing and close-out) and the growth and maintenance of the clinical research infrastructure (including Clinical Trial Management System implementation and maintenance) for the organization. The Director is responsible for developing and overseeing organizational strategy and goals, providing strategic leadership, building and modeling a high-performance culture with strong engagement within sub-departments. Intermediary between the sponsor, study PI and ACRI contracts office to ensure legal documents are processed.
Additional Information:
Provides strategic and operational leadership for a large, multidisciplinary clinical research organization of 100+ staff. Oversees the full clinical research portfolio, including study start-up, regulatory, coordination, research nursing, and financial operations, as well as the clinical research technology ecosystem.
Leads organizational strategy, drives operational excellence, and fosters a high-performing, engaged culture. Serves as a key liaison to leadership, sponsors, and partners, strengthening collaboration and advancing research operations. Ensures effective governance, financial oversight, compliance, and process standardization to support data-driven decisions and a high-quality, efficient research enterprise.
Required Education:
Bachelor's Degree
Recommended Education:
Master's Degree
Required Work Experience:
Related Field - 7 years with 5 years of leadership experience
Recommended Work Experience:
Required Certifications:
Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals
Recommended Certifications:
Registered Nurse (RN) license - Arkansas or Compact State
Description
1. Leads a multidisciplinary clinical research organization, partnering with internal and external investigators, institutional leadership, and key stakeholders to advance research initiatives.
2. Drives strategic growth of clinical research by developing and executing a multi-year clinical trials strategy; establishes annual targets for study start-up, enrollment, capacity, and throughput, and leads change management efforts to scale operations.
3. Oversees clinical research operations across multiple sub-departments, including clinical research coordination, pediatric clinical research unit, investigational drug services, regulatory services, study start-up, budget development and negotiation, and research systems utilization.
4. Ensures regulatory compliance and operational excellence by applying deep knowledge of federal regulations and the clinical research environment to support safe, efficient, and high-quality research with a strong focus on transparency, customer service, and continuous improvement.
5. Serves as the primary operational liaison with internal and external partners, including ACRI, ACH, UAMS, sponsors, CROs, consortia, and clinical leadership; promotes clinical research operations, expands partnerships, attracts sponsors, supports funding opportunities, and strengthens investigator engagement, performance, and integration.
6. Establishes and governs research operations frameworks, including centralized feasibility, pipeline management, and study prioritization; optimizes resource allocation through workload and capacity modeling to improve activation and enrollment timelines.
7. Builds and leads a high-performing team by overseeing recruitment, training, performance management, and engagement initiatives; fosters a collaborative, inclusive, and results-driven culture.
8. Partners across departments to standardize and enhance research feasibility and start-up processes; ensures compliance with regulatory, financial, and legal requirements while maintaining continuous inspection readiness.
9. Provides financial leadership for clinical research operations, including budgeting, forecasting, pricing, coverage analysis, compliant billing, invoicing, and accounts receivable; supports data-driven portfolio and investment decisions to expand and accelerate clinical research.
10. Performs other duties as assigned in alignment with the scope and level of the role.

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