Assistant Clinical Trial Navigator (Temporary)

Javara Inc.; South Carolina; On-site; USD 42,000 - 64,000; Part time

Job summary

Javara Inc. in the United States is seeking a temporary Assistant Clinical Trial Navigator to support coordination and administration of clinical trials under the Manager of Site Operations and the Principal Investigator.

You will focus on achieving enrollment goals while upholding patient safety and data quality in all study activities. Key duties include coordinating visits, assisting in informed consent, maintaining source data, and ensuring procedures comply with SOPs, GCPs, and regulatory

Qualifications

• Associates or Bachelor’s degree or equivalent experience.
• Experience coordinating clinical trials or related field preferred.
• Strong attention to data integrity and regulatory compliance (GCP, SOPs).

Responsibilities

• Assist with coordinating and scheduling patient visits per protocol.
• Support enrollment goals by contributing to enrollment strategies and patient experience.
• Ensure accurate data capture, source documentation, and timely query resolution.
• Adhere to SOPs, GCPs, OSHA and other regulatory requirements.
• Assist with informed consent process and maintaining study documentation.
• Travel up to 30% regionally as needed.

Skills

Coordination

Communication

Teamwork

Customer service

Data integrity

Regulatory compliance

Education

Associates or Bachelor's Degree

Tools

CTMS

Electronic reporting systems

Job description

Job Description: As a temporary 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.

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.

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.

We're thrilled that you're considering joining #TeamJavara. Our team is passionate about breaking barriers to make a true difference in the world and address unmet needs of patients through clinical research as a care option.

Javara is dedicated to fostering a culture of teamwork and collaboration while embracing and celebrating diversity.

Whether you're a seasoned professional or just starting to explore clinical research as a career, you will have the opportunity to be part of cutting-edge research that has the potential to shape the future. Join us in our pursuit of excellence as we unlock new insights, solve complex challenges, and drive positive change for both our patients and trusted healthcare partners. Your journey towards a fulfilling career in clinical research starts here.

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.