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Director Clinical Research Operations Jobs (NOW HIRING)

Research Operations Managers/Supervisors (as applicable); Clinical Research Coordinators and ... Direct research administration, quality assurance, compliance monitoring, education, and continuous ...

Flint, MI Job Id: 2496 # of Openings: 1 Insight Health System Clinical Research Associate Director, Research Operations Title: Associate Director - Research Operations Location: Michigan Reports To:

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Director Clinical Research Operations information

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

As of Aug 10, 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 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 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 clinical research operations?

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:
Infographic showing various Director Clinical Research Operations job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $145,969 per year, or $70.2 per hour.

Director, Clinical Research Operations and Strategy

CARTI, Inc.

Little Rock, AR

Full-time

Re-posted 9 days ago


CARTI rating

8.0

Company rating: 8.0 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

JOB SUMMARY: The Director of Clinical Research Operations and Strategy is a senior business and program leadership role responsible for the development, execution and growth of CARTI's clinical research enterprise to serve a diverse and geographically dispersed population, including rural and underserved communities. In co-leadership with the Medical Director of Clinical Research and reporting directly to the Chief Clinical Officer, this position serves as the operational and strategic anchor of the CARTI research pillar - translating scientific opportunities into an executable, financially sustainable, and sponsor-attractive trial portfolio. This role collaborates closely with the executive leadership, including the CFO, physician investigators, and external partners to align research strategy with organizational priorities and ensure scalable, high-quality program performance.

SPECIFIC JOB DUTIES AND RESPONSIBILITIES:

  1. Develop and manage CARTI's clinical trial portfolio, evaluating studies for scientific alignment, financial viability, and operational feasibility
  2. Collaborate with executive and clinical leadership to define research strategy, growth priorities, and new program development
  3. Support expansion into emerging areas, including theranostics, bispecifics, device-based therapies, and precision medicine
  4. Cultivate and maintain relationships with pharmaceutical sponsors, biotech companies, device manufacturers, and contract research organizations (CROs) to position CARTI as a preferred investigational site
  5. Lead site qualification and feasibility processes for sponsor-initiated studies
  6. Serve as the primary operational liaison for external research partnerships
  7. Oversee day-to-day research program operations including study activation, patient enrollment performance, data quality, and protocol compliance across all active trials
  8. Partner with investigators to align research opportunities and support investigator-initiated trial development
  9. Direct the research operations team establishing performance standards, workflows, and capacity planning
  10. Ensure that all CARTI research-related committees (CSSC, PRMC, Genetic/Genomic, Grant and Publication Committees) operate as a coordinated system aligned with strategic priorities, regulatory requirements and operational efficiency.
  11. Develop and manage the research program budget, including trial-level financial modeling
  12. Lead sponsor contract and budget negotiations
  13. Oversee Medicare Coverage Analysis and ensure compliant billing practices
  14. Monitor KPI and prepare financial reporting on research program performance for leadership
  15. Identify and pursue federal, state, and foundation grant opportunities (e.g. NCORP, FDA-funded initiatives, and rural health research initiatives)
  16. Lead or co-lead grant applications and funding strategies
  17. Manage grant reporting, compliance, and financial reconciliation
  18. Ensure compliance with GCP, FDA regulations, IRB requirements, and institutional SOPs across all active studies
  19. Maintain high standards for data integrity, audit readiness, and regulatory adherence

OTHER JOB REQUIREMENTS: N/A

SUPERVISORY RESPONSIBILITY: Yes

EDUCATION, CERTIFICATION, LICENSURE, REGISTRATION:

  1. Bachelor's degree in health sciences, life sciences, business, or related field; Master's degree (MPH, MS, MHA, MBA) with clinical/research foundation, preferred
  2. CCRP (Certified Clinical Research Professional) CCRC, or equivalent certification preferred

EXPERIENCE, KNOWLEDGE, SKILLS and ABILITIES:

  1. Minimum seven (7) years of clinical research experience, including five (5) years in a leadership role.
  2. Demonstrated success in building, scaling and managing a clinical trial portfolio, including sponsor-facing business development or site selection participation
  3. Strong working knowledge of GCP, FDA regulatory framework, IRB processes, and Medicare Coverage Analysis
  4. Experience with clinical trial budget development and sponsor contract negotiation
  5. Strong communication and relationship management skills; ability to engage credibly with sponsors, physician investigators, executive leadership, and external funders
  6. Experience with NCI NCORP, NIH grant mechanisms, or state health department research funding, preferred
  7. Oncology-specific research background, preferred
  8. Familiarity with device/IDE trial regulations, particularly in emerging therapeutic areas, preferred
  9. Experience operating in a community-based or rural health care setting, preferred

REASONING ABILITY:

  1. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
  2. Ability to interpret a variety of instructions furnished in written, oral, or schedule form.

INTERPERSONAL SKILLS:

  1. Must interact and communicate both verbally and in written form.
  2. Must interact and exchange information regarding patients with physicians and other departmental personnel, and outside agencies on a frequent basis while respecting the confidentiality of patient information.

PHYSICAL DEMANDS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

  1. While performing the duties of this job, the employee is regularly required to talk or hear.
  2. The employee regularly is required to stand, walk, sit, use hand to finger, handle or feel objects, tools, or controls; and reach with hands and arms.
  3. Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

The work environment described here are representative of those an employee encounters while performing the essential functions of this job. This position involves potential exposure to infectious diseases. Team members are offered appropriate vaccinations and safety training.

This position is a Safety Sensitive Position. The essential functions, physical demands, and mental competencies of this job require the employee maintain the ability to work in a constant state of alertness in a safe manner.


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