Assistant Clinical Trial Navigator

Javara Inc.; Fort Worth, Northern (TX, KY); Hybrid; USD 42,000 - 56,000; Full time

Job summary

Javara Inc. seeks an Assistant Clinical Trial Navigator in Fort Worth, TX to assist with coordinating and administering clinical trials. You will support patient enrollment goals and maintain trial documentation with a focus on participant safety and data integrity.

You will report to the Manager of Site Operations and the Principal Investigator, coordinating visits, assisting with consent, and following SOPs and regulatory requirements. Some travel is required.

Qualifications

• Associates or Bachelor’s Degree in related field or equivalent experience beneficial.
• Experience in clinical trials is advantageous.

Responsibilities

• Assist with coordination and administration of clinical trials ensuring participant safety.
• Support enrollment goals by contributing to enrollment strategies and building relationships with patient populations.
• Assist in informed consent process and maintain study documentation up to date and audit-ready.
• Document data in CTMS and supplier systems, including source data and query resolution.
• Coordinate and schedule patient visits and collect/handle clinical samples as needed.
• Travel up to 30% regionally as required.

Skills

Patient enrollment

Clinical coordination

Communication

Regulatory awareness

Education

Associate or Bachelor’s degree in related field

Job description

## Assistant Clinical Trial NavigatorApply: Fort Worth, TX: Full time: Posted 3 Days Ago: R-100266**Job Description:**As an Assistant Clinical Trial Navigator with Javara, you will assist with the coordination and administration of clinical trials and report to the Manager of Site Operations and the Principal Investigator or designee. You will participate in achieving and exceeding patient enrollment goals with a dedication to quality and integrity. With a guiding principle of research participant safety, you will assist with implementing and coordinating research study procedures for the successful management of clinical trials.**Essential Responsibilities:*** Seek to improve the patient’s experience, never compromising on safety.* Provide excellent customer service to patients and participants, healthcare partner and practice stat investigators, sponsors, and vendors.* Support enrollment goals by contributing to enrollment strategies, striving to provide exceptional experiences for patients, and building relationships with local patient populations.* Assist with patient identification and recruitment as needed.* Assist in strengthening efficient working relationships with colleagues, patients, investigators, and other internal and external partners.* Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution.* Assist with ensuring study documentation is up to date and audit ready.* Adhere to all Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), protocols, OSHA, proper PPE usage and other regulatory authority requirements.* Assist with conducting and documenting the informed consent process.* Demonstrate continuous commitment to learning and developing skill sets and knowledge base as it relates to clinical trial operations and the patient experience.* Coordinate and schedule patient visits and conduct visits per protocols.* Assist with performing clinical and laboratory skills such as therapeutic area specifics, obtaining vitals, EKGs, and collecting, processing, and shipping bodily samples.* Demonstrate our Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.* Additional tasks as assigned.**Qualifications:*** Associates or Bachelor’s Degree in related field or equivalent experience highly beneficial.**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.**Travel:** This position may require up to 30% travel regionally but may occasionally include travel to other regions or 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.