Clinical Trial Navigator
$47.4k - $118.6kIQVIA
Location Office based in Irving, TX. Job Summary Under the direction and supervision of the Assistant Director of Clinical Trial Management, this position is responsible for assisting patients by coordinating referral appointments. The CTN performs general clerical tasks such as answering phone calls and emails, maintaining patient records, and verifying insurance information. The position works closely with new patients, referral physician offices, NEXT physicians, research coordinators and medical records team in support of all ongoing clinical studies. Essential Duties and Responsibilities Demonstrates an understanding of patient/sponsor confidentiality to protect the patient and practice. Following HIPAA guidelines gathers patient records from a variety of sources (i.e., portal systems, mail, fax/eFax, email, etc.), which will require interacting with medical records departments, registration areas, and/or physicians' offices in a professional manner. Keeps health care providers and research personnel within practice informed by communicating availability or unavailability of the records. Handles medical record requests and related releases of information ensuring that all releases are compliant with HIPAA guidelines. Serves as a backup to the CTNs at other NEXT sites to ensure proper coverage. Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. Schedules and arranges referral appointments. Sets appointments, sends reminders, and provides patients with information about new patient visits. Maintains ongoing tracking and appropriate documentation on referrals to promote team awareness and ensure patient safety. Ensures complete and accurate registration, including patient demographic and current insurance information. Ensures that referrals are addressed and facilitates timely scheduling of appointments. Assembles information concerning patient's clinical background and referral needs. Contact organizations and insurance companies to ensure prior approval requirements are met. Present necessary medical information such as history, diagnosis, and prognosis. Assists patients in problem solving potential issues related to the health care system, financial or social barriers (e.g., request interpreters as appropriate, transportation services or prescription assistance). Obtains up to date insurance information and ensures preauthorization for new patient visits. Attends meetings and briefings regarding clinical studies as required. Ability to maintain a positive attitude with the research team. Maintain professional demeanor with clients and outside medical records facilities. Remains current with all required training. Performs other duties as assigned Knowledge, Skills and Abilities Knowledge of Phase I oncology clinical research. Knowledge of appropriate software including Microsoft suite applications and Adobe Acrobat Pro. Excellent interpersonal skills to deal effectively with research personnel. Knowledge of medical terminology. Knowledge of ICH GCP, FDA, OHRP, OSHA and HIPAA guidelines pertaining to clinical research. Excellent organizational skills to independently manage workflow. Ability to prioritize quickly and appropriately with minimal guidance. Ability to multi-task, work independently and function as part of a team. Clear and concise verbal and written communications. Required Education and Experience Minimum of BS preferably in Health Sciences. EEO Statement IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. EEO Minorities/Females/Protected Veterans/Disabled Compensation The potential base pay range for this role, when annualized, is $47,400.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. #J-18808-Ljbffr IQVIA
- ...caregivers who are seeking, considering, or participating in clinical trials at the Simmons Comprehensive Cancer Center. This role helps... ...Experience : o Experience in oncology, clinical research, navigation, or patient-facing support role. o Experience utilizing...SuggestedFull timeWork experience placement
- ...protocols, multidisciplinary plan of care, and clinical area specific standards. Must... ...health care professionals to optimally navigate the health care system. Seeks and utilizes... .... Keeps abreast of current clinical trials relevant to the patient population and specific...SuggestedFull timeContract workTemporary work
$105k - $118k
...Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience... ...provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical...SuggestedWork at officeLocal areaRemote workNight shift- ...Associate Clinical Trial Manager Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is...SuggestedFull timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...Join one of the world's largest Clinical Research Organizations and support early-phase clinical trials in a fastpaced, highly collaborative environment. As a Clinical Research Coordinator, you will oversee the operational execution of assigned studies, ensuring compliance...SuggestedFull timePart timeWork at office
- ...assessments. If you are a motivated professional with a passion for clinical research and patient engagement, we invite you to apply!... ...research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of...H1bWork at office
$50k - $60k
...Clinical Nurse Coordinator (LPN) Compensation: $50,000 - $60,000 annual salary, plus annual... ...Coordinator (LPN), you'll support care navigation across the continuum of cancer by... ...department, you'll also assist with clinical trial participation, manufacturer assistance...Full timeLive inRemote workFlexible hoursNight shiftWeekend workAfternoon shift- (Onsite in DeSoto, TX) Our client is a rapidly growing clinical trial site network focused on advancing life-changing therapies through high-quality research, patient safety, and diverse enrollment. The organization specializes in late-phase, industry-sponsored psychiatric...
- ...US Oncology Inc. is seeking a Data Coordinator for the Dallas Sammons location. This hybrid role involves managing clinical trial data, ensuring compliance with regulations, and maintaining research protocols. Qualified candidates should have a High School Diploma, with...
- ...Travel Percentage: Negligible Job Shift: Day Job Category: Research Clinical Research Assistant will perform work in one or all of the... ...Research Assistant will assist in the management of multiple clinical trials according to the study protocol, perform collection of clinical...Full timeWork experience placementWork at officeLocal areaShift work
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality... ...treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients...Work at officeLocal areaFlexible hours
- ...Clinical Research Coordinator Dermatology Treatment and Research Center (DTRC) - Dallas, TX 75230 Position Type: Full Time Job Shift... ...coordinators are responsible for conducting clinical research trials by adhering to Good Clinical Practice (GCP), International Air...Full timeContract workShift work
- ...Dermatology Partners is a network of high-quality dermatology clinics that focus on collaborative and innovative ideas to drive growth... ...responsible for perfoming all administrative aspects of clinical trial research studies based upon needs and goals of the Research Program...Temporary workWork at office
- ...Summary: The Clinical Research Coordinator (CRC) manages and coordinates clinical research studies, ensuring they are conducted efficiently... ...staff, and study participants to oversee all aspects of trials, including recruitment, data management, regulatory compliance,...Local area
- ...Job Purpose This position will be located in the Dallas Main Office and will report directly to the Clinical Operations Officer. The position will help to identify, evaluate, and recruit potential patients for ongoing studies and is responsible for managing data collection...Work at office
- ...Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the... ...Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more; ~...Contract workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
$78k - $130k
...A multinational clinical research organization is seeking a Lead Clinical Research Associate (CRA) who will be responsible for managing clinical site monitoring services on a multinational scale. The successful candidate must be fluent in both English and French and possess...Remote work$78k - $130k
...fluent in English and French. Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may... ...recruit site investigators, coordinate the movement and delivery of trial materials, samples, tests and forms, including investigational...Remote workWork from home- ...Position: Senior Clinical Research Associate (CRA) – Study Startup & Monitoring Oversight Location: U.S.-based candidates in Central... ...activities and provide monitoring oversight across oncology clinical trials. This role is ideal for someone who thrives in a fast-paced...Full timeContract workTemporary work
- Direct Jobs is looking for a Clinical Research Coordinator 1 to assist Principal Investigators with all phases of clinical trials in Dallas, Texas. This entry-level position involves implementing research protocols, ensuring compliance with guidelines, and conducting quality...
- A leading clinical research organization in Dallas is looking for a Clinical Research Coordinator I to manage daily operations of clinical trials. Responsibilities include participant recruitment, ensuring compliance with regulatory requirements, and maintaining data confidentiality...
- We are looking to add a full time onsite Clinical Research Coordinator to a growing research site. Qualified candidates will have a minimum... ...collected from subjects in connection with a clinical research trial Entering patient and research data in systems designated by...Full timeLocal area
- ...a rewarding career! JOB SUMMARY The UT Southwestern Clinical Research Coordinator Fellowship is a two-year program that trains... ...collection tools. May coordinate regulatory aspects of the trial including maintaining and developing regulatory information to...Full time
- Clinical Research Assistant I Works under the direction of an Investigator(s) with general supervision, to primarily provide ongoing data... ...and protocol requirements for routine and low complexity trials (e.g., questionnaire, data registry, scripted); schedules research...Full timeLocal area
- Education and Experience Education and Experience Requirements: Must be eligible to work in the U.S.; H1b visa holders are ineligible More than 4 years of research experience; or 3+ years of research experience and a Bachelor Degree in a relevant area; or 3+ years of...H1bWork at officeLocal area
- ...Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials. As Revival ResearchInstitute is growing, we are looking to add more qualified professionals to our team, who are looking...Full timeWork at office
- ...education, and referrals. Serves as a resource and role model for clinical practice, training, evaluation, and direct management of... ...projects. May participate in clinical research or clinical drug trials. Assists in developing, implementing, and monitoring annual...TraineeshipShift workDay shift
- Overview Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies and clinical... ...applicable procedures and timeframes Interact with the Trial Start-up team and support collecting the documents or information...Work at officeRemote work
- ...Senior Clinical Trial Manager The Senior Clinical Trial Manager provides strategic and operational leadership for global clinical programs, with a focus on renal denervation (RDN) and cardiology clinical trials. This role leads Clinical Trial Managers and study teams...
- A leading clinical research organization seeks a Senior Clinical Research Associate in Dallas, TX. This role focuses on managing site activities, developing enrollment strategies, and ensuring compliance with study regulations. Ideal candidates will have a background in...Remote workWork from homeFlexible hours
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