Clinical Trial Navigator II

***Please note this is an on-site position that requires a minimum of two years of patent-facing experience in clinical trials. The annual salary range starts at $69,000 and is based on experience.

Summary:

The Clinical Trial Navigator (CTN)II is a specialized research professional responsible for the coordination and administration of clinical trials under the direction of the Manager of Clinical Trial Operations and the Principal Investigator or designee. The CTN II implements and coordinates research study procedures for the successful management of clinical trials.

Essential Duties and Responsibilities:

Promote the mission of Javara with a primary guiding principle of patient safety and well-being and building and maintaining a culture that combines the highest standard of integrity with excellence to all those Javara serves

Manage clinical research studies and adhere to Javara Standard Operating Procedures (SOPs), the healthcare partner’s SOPs, Good Clinical Practices (GCPs), study protocols, clinical trial agreements, and regulations governing clinical research

Coordinate research participant visits and study related procedures according to study protocol windows and study team schedules, which may involve handling travel logistics for research participants; ensure reminder communications (phone, text or email) are sent to promote research participant show rate and compliance; identify and outreach to prospective patients; prepare study visit materials such as lab kits, study forms and diaries for participant visits

Conduct clinical research study visits/procedures per protocol requirements. This may require obtaining vital signs, height, weight, EKG’s, spirometry, medical history, medications, adverse events and labs as well as administering questionnaires and diaries

Ensure scientific integrity of data and protect the rights, safety and well-being of research participants

Navigate the resources and workflow within the healthcare and clinical research environment to ensure seamless care for the clinical trial participant, to engage investigators in research daily and to promote clinical research within the healthcare system

Create and implement a patient engagement plan to identify and contact potential research participants, and then screen and enroll participants in suitable clinical research studies

Conduct and document the informed consent process when delegated to do so by the Principal Investigator in compliance with Javara’s SOPs

Collect, process and ship any bodily samples such as blood and urine as required per protocol in compliance with Javara’s SOPs, IATA guidelines and laboratory guidelines

Dispense investigational products and other research study supplies in an accountable manner in accordance with study requirements, institutional requirements, investigator approval and regulations.

Inform and educate the research team and healthcare system staff regarding study related procedures including IP dosing and monitoring requirements

Assist with Integrating clinical research as a care option within the healthcare system

Monitor and report adverse events, serious adverse events and protocol deviations to the investigator, sponsor, Javara Director and IRB in compliance with Javara’s SOPs

Know and understand regulatory requirements, maintain files and documents, and assist the Manager of Trial Activation with regulatory submissions

Create source documents as needed and document appropriately in source documents and /or medical records (paper, EMR, e-source) per ALCOA: data is attributable, legible, contemporaneous, original and accurate

Complete and maintain case report forms (paper or electronic) and answer queries regarding study data per FDA regulations, clinical trial agreement and protocol requirements

Prepare and participate in routine monitoring visits, internal and external audits, and inspections

Ensure study documentation is audit ready in the event of monitoring, audits and inspections

Assist with additional projects as requested by Director/ Associate Director of Clinical Research Operations

Work with the Manager of Clinical Trial Operations to ensure that all functions are aligned with the company’s strategic mission, values, and vision

Demonstrate the ability to multi-task and flexibility to manage multiple clinical trials and/or assist team members in high volume/complex trials.

Qualifications:

Required

Minimum Bachelor’s degree or 2 years of related experience

At least 4 years of experience in healthcare and/or related field

Knowledgeable of study specific protocols as well as regulations and guidance for the conduct of clinical trials per the ACRP Core Competency Guidelines

Effectively manages multiple priorities with confidence while consistently demonstrating excellent client service

Ability to demonstrate competency with respect to both clinical trial conduct and specific research studies with investigators, healthcare partners, sponsor, CRO, research team, and potential and active research participants

Exceptional time management, problem-solving, planning and organizational skills

Strong interpersonal skills with proven written and verbal communication skills; practices strong documentation techniques; consistently and effectively educates participants of the informed consent process and the phases and purpose of the study; articulates the various roles in the process, provides sound direction and keeps participants well informed, promoting high participant engagement; guides others in this area

Effectively works autonomously or as part of a team with ability to properly train Assistant CTN-As and CTNs, as needed.

Ability to manage multiple priorities while demonstrating excellent client service

Fluent in the use of Microsoft Office applications

Comfort and ability in the use of standard office equipment such as computers, laptops, tablets, phones, photocopiers, and printers

Preferred

Bachelor’s degree in related field

Clinical Research Coordinator Certification from the ACRP

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 involve up to 25% travel within the USA and other countries for 2–3-day trips at least 6 times per year. Travel includes trips between research centers, medical practices, and Javara’s headquarters office.

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.