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Manager, Site Operations

Javara


Job Location:

Fayetteville, GA - USA

Monthly Salary: Not provided by the employer
Posted: 3 July 2026 (30+ days ago)
Application Deadline: 30 September 2026
Vacancies: 1 Vacancy

Job Summary

Job Description:

Essential Responsibilities:

  • Promote a culture that ensures patient safety above all and improves the patient experience in everything we do.

  • Drive accountability for patient enrollment ensuring Clinical Trial Navigators own the enrollment plan to meet recruitment goals for their specific studies.

  • Ensure the highest standard of integrity quality and operational excellence in clinical research activities with adherence to Standard Operating Procedures (SOPs) Good Clinical Practices (GCPs) protocols OSHA Integrated Research Agreements (IRAs) and other applicable federal state and local regulations.

  • Positively impact engagement retention and the employee experience by demonstrating the core behaviors for people managers in three key pillars: Engage & Inspire Drive Success and Empower & Develop.

  • Recruit train manage and coach Site Operations team members and ensure they meet expectations in accordance with role expectations and company goals.

  • Maintain a staffing plan for resourcing and utilization of site operations team members for multiple locations or larger sites to achieve performance objectives identify opportunities or gaps and implement plans accordingly.

  • Oversee the standardized utilization of systems data entry and clinical trial operations best practices.

  • Cultivate maintain and develop strong long-term relationships with investigators and practice staff and provide insight on the best clinical trials for their patient population.

  • Maximize research participant identification enrollment retention and ongoing engagement by developing programs and processes including training and accessing EMR to assess viability of enrolling in trials.

  • May manage multiple sites or satellite site locations.

  • Provide high quality client support to build credibility and trust while meeting the needs and strategic objectives of healthcare partners sponsors CROs patients vendors and colleagues.

  • Manage study and site performance including developing and adhering to an operating budget for clinical trial operations within the healthcare organization as well as budgets associated with clinical trials.

  • Other responsibilities as assigned.

Qualifications:

  • 2 years experience managing a clinical research site and team or equivalent relevant management experience.

  • 5 years of clinical trial research experience including hands-on application of clinical functions such as obtaining vitals EKGs and phlebotomy.

  • Associates or Bachelors Degree or equivalent educational experience. Degree in Life Sciences or related field highly beneficial.

  • Experience applying leadership approaches such as situational leadership servant leadership and transformational leadership for people management.

  • Experience using business acumen to develop strategies to achieve and exceed expected results.

  • Project Management

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

  • This job operates in a professional environment.

  • The noise level in this work environment is usually light to moderate.

Physical Demands:

The physical demands described here are representative of those that must be met to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.

  • The employee will regularly use hands to reach handle or feel objects tools or controls and talk and hear.

  • The employee may frequently stand walk and sit.

  • The employee may occasionally lift and/or move up to 25 pounds.

  • Specific vision abilities include close vision distance vision and the ability to adjust focus.

Travel: This position may involve up to 20% travel with most travel within their region as well as applicable visits to Javara headquarters in Winston Salem NC.

Pre-Employment Screening:Drug screen and background check .

This job description covers the most essential functions of this position and is not designed to contain a comprehensive listing of activities duties or responsibilities that are required of the employee in this job. Duties responsibilities and activities may change at any time with or without notice.

Javara is an integrated research organization (IRO) that advances value by integrating clinical research within the healthcare ecosystem. Javara brings better outcomes for patient centered care better economic results improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.

Equal Employment Opportunity Statement: Javara provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.


Required Experience:

Manager


About Company

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Javara is an Integrated Research Organization (IRO) changing the clinical research experience and expanding access to research for patients and providers.

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