Hiring.Camp

Director Clinical Research Operations

Archildrens

·

Apr 14, 2026

Location
Little Rock, United States of America
Type
Full-time
Department
Healthcare
Seniority
Director
Education
Master
Source
Workday

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.

  

Skills

WorkdayClinical TrialsAccounts ReceivableComplianceNegotiationChange Management

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