Manager, Site Operations

Posted 20 Days Ago
Be an Early Applicant
Fayetteville, NC, USA
In-Office
Senior level
Biotech
The Role
Lead and manage site operations for clinical trials, ensuring patient safety, regulatory compliance (GCP, SOPs), enrollment targets, staff hiring/training, site performance, budget oversight, stakeholder relationships, and standardized use of systems and data across one or multiple sites.
Summary Generated by Built In

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, EKG’s, 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 required include close vision, distance vision and the ability to adjust focus.  

TravelThis 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 required.  

 

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.

Skills Required

  • 2+ years managing a clinical research site and team or equivalent management experience.
  • 5+ years clinical trial research experience including hands-on vitals, EKGs, and phlebotomy.
  • Associate's or Bachelor's degree or equivalent educational experience.
  • Degree in Life Sciences or related field (highly beneficial).
  • Experience applying leadership approaches (situational, servant, transformational).
  • Demonstrated business acumen to develop strategies to achieve and exceed results.
  • Project management experience.
  • Pre-employment drug screen and background check.
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The Company
HQ: Winston-Salem, North Carolina
185 Employees
Year Founded: 2018

What We Do

As a leading Integrated Research Organization (IRO), we partner with major healthcare systems to embed clinical trials at the point of care, connecting patients to research through physicians they already trust, in the communities they already love. Our model unlocks access to broader, more diverse populations, driving faster enrollment, stronger retention, and richer data. With centralized resources and streamlined operations, we accelerate study start-up and reduce friction across the research lifecycle. Javara drove the evolution of Clinical Research as a Care Option (CRAACO) because we believe research should be accessible, inclusive, and seamlessly integrated into healthcare. Today, we’re delivering on that vision, plus so much more.

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