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ADAPTED_NOW

As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).

HOUR

Company DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.Due to our continued growth, we are hiring for a  Clinical Research Coordinator  at  Wake Research,  an M3 company.  This position is on-site and located in Las Vegas, NV.   Job DescriptionThe Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI).  While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.  Essential Duties and Responsibilities:<ul><li>Assisting trial Investigator in screening and review of potential study participants eligibility</li><li>Maintaining case report forms, charts and documentation</li><li>Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants</li><li>Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements</li><li>Collecting and entering data as necessary</li><li>Assist management with potential new hire selection and shadowing process</li><li>Assist with study start-up, maintenance, and close-out of studies as needed for those on the team</li><li>Ability to be flexible with study assignments</li></ul> Qualifications<ul><li>Clinical Research Coordinator with at least two years of relevant experience</li><li>Phlebotomy experience is highly preferred</li><li>Previous experience as a medical assistant, LPN, or RN</li><li>Excellent verbal & written communication skills</li><li>Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking</li><li>Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines</li><li>Extensive clinical trial knowledge through education and/or experience</li><li>Successful completion of GCP Certification and Advanced CRC preferred</li><li>Detail-oriented</li><li>Familiarity with the Code of Federal Regulations as they pertain to human subject protection</li><li>Strong interpersonal skills</li></ul> Additional Information About M3: M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA. Benefits: A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:<ul><li>401(k), 401(k) matching</li><li>Dental insurance</li><li>Disability insurance</li><li>Employee assistance program</li><li>Flexible spending account</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>*M3 reserves the right to change this job description to meet the business needs of the organization*This position offers a competitive salary of $25/hr - $35/hr.#LI-Onsite#LI-LB1

Wake Research

Clinical Research Coordinator

Biology

Biotech and Pharmaceutical

Case Report Form (CRF)

Clinical Data

Clinical Research

Clinical Trial

Clinical Trial Management

Code of Federal Regulations

Communication Skills

Conduct Studies

Contract Research Organization (CRO)

Data Collection

Data Entry

Dental Insurance

Detail Oriented

Documentation

Employee Assistance Plan

GCP (Good Clinical Practices)

HIPAA (Health Insurance Portability and Accountability Act)

Healthcare

International Health

Interpersonal Skills

Licensed Practical Nurse/Licensed Vocational Nurse

Market Research

Medical Assistance

Medical Equipment

Mentoring

Multitasking

Network Integration

Organizational Skills

Patient Confidentiality

Phlebotomy

Presentation/Verbal Skills

Process Improvement

Regulations

Regulatory Compliance

Research Protocols

Startup

Writing Skills

nas_musaorganic

FEED

The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Job Summary:We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.Key Responsibilities:<ul><li>Coordinate day-to-day clinical research activities to ensure study protocols are followed.</li><li>Recruit, screen, and enroll study participants.</li><li>Obtain informed consent and ensure ethical conduct in all study interactions.</li><li>Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).</li><li>Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).</li><li>Maintain accurate and timely documentation in case report forms and electronic databases.</li><li>Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.</li><li>Schedule participant visits and follow-ups; ensure visit windows are met.</li><li>Ensure proper storage, handling, and accountability of investigational products, if applicable.</li><li>Maintain regulatory documents and assist with IRB submissions.</li></ul>Qualifications:<ul><li>Bachelor's degree in a health-related field required.</li><li>At least 1–2 years of experience in clinical research preferred.</li><li>Phlebotomy certification or MA certification preferred.</li><li>Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.</li><li>Excellent organizational skills and attention to detail.</li><li>Strong interpersonal and communication skills.</li><li>Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).</li><li>Ability to work independently and as part of a multidisciplinary team.</li></ul>Preferred Qualifications:<ul><li>Experience working in clinical trials, especially in a hospital or academic setting.</li><li>Familiarity with IRB processes and clinical trial documentation.</li><li>Bilingual skills (depending on patient population) may be a plus.</li></ul>

ECN Operating LLC

Biological Processes

Certified Medical Assistant

Clinical Assessment

Clinical Data Collection

Clinical Study Publications

Collections Regulations

Cross-Functional

Electrocardiogram

Electronic Data Capture (EDC)

Hospital

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Informed Consent

Investigational New Drug (IND)

Microsoft Office

Multilingual

Sample/Specimen Processing

Specimen Collection

Time Management

clearcompany

OTHER

The Clinical Reviewer reviews diagnostic imaging and pulmonary testing orders in accordance to reimbursement guidelines and obtains necessary pre-certifications and exceptions to ensure no delay in reimbursement of treatments. Obtains insurance authorization and pre-certification for imaging, pulmonology and surgical services; works as a patient advocate and functions as a liaison between the patient and payer to answer reimbursement questions and avoid insurance delays.

Overview:
<img alt="CCCN Vertical Logo" src="https://theusoncologynetwork.icims.com/icims2/servlet/icims2?module=AppInert&action=download&id=141115&hashed=-1293135015" style="margin-left:auto;margin-right:auto"/>At Comprehensive Cancer Centers of Nevada (CCCN) a distinguished team of doctors, researchers, nurses and healthcare professionals have provided patients with groundbreaking treatments on the healing edge of medicine for over 50 years. Our team is dedicated to providing the most effective treatments, both existing and emerging, in order to diagnose and successfully treat cancer and blood disorders. We support this goal with state-of-the-art facilities across Southern Nevada, all of which integrate the latest diagnostic, therapeutic and research capabilities.  CCCN is dedicated to patient-centered care, advancing innovation, discovery, and improving outcomes.  Motivated, caring professional are encouraged to join us. Career Opportunity:Comprehensive Cancer Centers of Nevada is seeking a Clinical Insurance Reviewer to work remotely in the Southern Nevada area only. The Clinical Reviewer reviews diagnostic imaging and pulmonary testing orders in accordance to reimbursement guidelines and obtains necessary pre-certifications and exceptions to ensure no delay in reimbursement of treatments. Scope:Under general supervision, reviews chemotherapy regimens in accordance to reimbursement guidelines. Obtains necessary pre-certifications and exceptions to ensure no delay in reimbursement of treatments. Researches denied services and alternative resources to pay for treatment. Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.

Responsibilities:
ESSENTIAL DUTIES AND RESPONSIBILITIES: <ul><li>Reviews, processes and audits the medical necessity for each patient radiation oncology treatment, imaging and testing requests</li><li>Communicates with nursing and medical staff to inform them of any restrictions or special requirements in accordance with particular insurance plans. Provides prompt feedback to physicians and management regarding documentation issues and payer issues with non-covered or denied services</li><li>Updates coding/payer guidelines for clinical staff</li><li>Obtains insurance authorization and pre-certification for imaging, pulmonology and surgical services; works as a patient advocate and functions as a liaison between the patient and payer to answer reimbursement questions and avoid insurance delays.</li><li>Researches additional or alternative resources for non-covered chemotherapy services to prevent payment denials. Provides a contact list for patients community resources including special programs, drugs and pharmaceutical supplies and financial resources.</li><li>Maintains a good working knowledge of authorization requirements for all payers, State and federal regulatory guidelines for coverage and authorization</li><li>Adheres to confidentiality, state, federal, and HIPPA laws and guidelines with regards to patient's records</li><li>Other duties as requested or assigned</li></ul>

Qualifications:
MINIMUM QUALIFICATIONS: <ul><li style="margin-bottom:0in">High school diploma or equivalent required</li><li style="margin-bottom:0in">Associates degree in Healthcare, LPN state license and registration preferred</li><li style="margin-bottom:0in">Minimum three (3) years medical insurance verification and authorization required</li></ul> PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is required to be present at the employee site during regularly scheduled business hours and regularly required to sit or stand and talk or hear. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range. WORK ENVIRONMENT: The work environment may include exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment. Work will involve in-person interaction with co-workers and management and/or clients. Work may require minimal travel by automobile to office sites.Successful candidates will thrive in a fast-paced, rapidly changing environment and have a passion for caring for their patients.    Ready For Your Next Career Challenge?  We’d Love to Hear from You! If you possess the above qualifications and a desire to make a difference, we invite you to submit your resume and apply.  In addition to a great career opportunity, we offer excellent benefits, a team environment, professional development, and the chance to be part of a nationwide network dedicated to fighting the war against cancer.  To apply please click on the “Apply” link.  The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status. This employer participates in E-Verify.

Comprehensive Cancer Centers of Nevada

Prior Authorization Specialist/Clinical Insurance Reviewer - Remote ( Southern Nevada only)

Blood Disorders

Cancer

Chemotherapy

Clinical Validation

Denial of Service (DoS)

Federal Laws and Regulations

Health Insurance

Hearing Impairment

Hematology

High School Diploma

Identify Issues

Infectious Diseases

Insurance

Lift/Move 40 Pounds

Manual Dexterity

Medical Imaging

Medical Records

Medicine

Nursing

Oncology

Patient Care Authorizations

Patient Care Denials

People Management

Physical Demands

Quality of Care

Radiation Therapy

Reimbursement

Reimbursement Guidelines

Research Nursing

Respiratory Medicine

State Laws and Regulations

Willing to Travel

Work From Home

[AW]-iCims

You will provide virtual sessions, assess client needs, and help clients move through therapy, psychosocial assessment, treatment planning, and steady behavioral health support with care, structure, and realistic goals. · Master's degree in a relevant behavioral health field appropriate for Licensed Clinical Social Worker licensure.

Licensed Clinical Social Worker (LCSW)<h3>Location and Role Details</h3>Location: Henderson, NevadaWork Setting: Remote / TelehealthPosition Type: Full-TimeSalary: $115,000-$120,000 per year with full benefitsSchedule: Monday-Friday, 9:00 AM-5:00 PM<h3>Job Summary</h3>This is a client-facing remote therapy role for a LCSW who wants dependable full-time work and a clear clinical focus. You will provide virtual sessions, assess client needs, and help clients move through therapy, psychosocial assessment, treatment planning, and steady behavioral health support with care, structure, and realistic goals.This position is a strong fit for a clinician who understands how mental health, stress, systems, and practical barriers can affect a client’s progress.<h3>Responsibilities</h3>·        Hold scheduled telehealth sessions with clients and provide practical therapeutic guidance·        Consider psychosocial factors, support systems, stressors, and client strengths during care planning·        Assess client concerns and translate them into clear treatment priorities·        Maintain clinical notes that reflect interventions, progress, and next steps·        Support clients with skill-building, reflection, and behavior change strategies·        Protect client privacy and maintain a professional virtual care settingRequirements·        Active Nevada LCSW license in good standing·        Master's degree in a relevant behavioral health field appropriate for Licensed Clinical Social Worker licensure·        Full clinical licensure required; temporary, associate, intern, or probationary licenses are not intended for this role·        A warm, ethical, and organized approach to therapy in a virtual setting.·        Experience with clinical social work, therapy, psychosocial assessment, or care planning is helpful.Benefits·        2 weeks PTO·        Health Insurance·        401K Plan with 3% Company Match·        Remote work structure designed for licensed cliniciansTake the next step toward a full-time telehealth role where your work can support clients with consistency and care.

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Clinical Research Associate Jobs in Nevada

Clinical Research Coordinator Wake Research

Clinical Research Coordinator ECN Operating LLC

Prior Authorization Specialist/Clinical Insurance Reviewer - Remote ( Southern Nevada only) Comprehensive Cancer Centers of Nevada

Licensed Clinical Social Worker (LCSW) Gotham Enterprises Ltd

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