Top 55 Nurse investigator Jobs in Houston, Tx

Clinical Nurse
IQVIA —Houston, TX
- $57,700 - $209,800 a year
- Full-time
- Nursing
- Vital signs
- OSHA
Nurse - Clinical Research Nurse
Tranquil Clinical and Research Consulting Services LLC —Webster, TX
- $60,000 - $95,000 a year
- Full-time
- Nursing
- LVN
- Computer literacy
- Paid time off
Quick Apply
Sub Investigator (NP)
DM CLINICAL RESEARCH GROUP —Houston, TX
- Nursing
- Management
- Patient monitoring
Registered Nurse
ECN Operating LLC —Houston, TX
- $35 - $50 an hour
- Part-time
- Mid-level
- 1 year
- Communication skills
Quick Apply
13d
LTCR Nursing Facilities Senior Investigator
Health & Human Services Comm —Houston, TX
- $6,947.66 - $8,886.16 a month
- Online Application
- Nursing
- RN License
- Nursing home
- Health insurance
- 401(k)
Quick Apply
Research Nurse (Pedi Surgery)
UTHealth Houston —Houston, TX
- Monday to Friday
- Nursing
- Surgery
- RN License
- Health insurance
- Employee discount
LTCR HCS Nurse Surveyor
Health & Human Services Comm —Houston, TX
- $7,474.23 - $8,886.16 a month
- Online Application
- Nursing
- RN License
- Word processing
- Health insurance
- 401(k)
Quick Apply
Research Nurse II-Part Time
Houston, Texas USA —Houston, TX
- $39,546 - $46,525 a year
- Part-time
- Spanish
- Nursing
- RN License
Clinical Research Coordinator II - Neurology Alzheimer
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Vital signs
- Hospital
- Customer service
8d
Senior Administrative Assistant - Nursing Education
MD Anderson —Houston, TX
- $21.87 - $32.93 an hour
- Full-time
- Management
- Mid-level
- Office
- AD&D insurance
- Paid holidays
Clinical Research Assistant
Pinnacle Clinical Research —Houston, TX
- Full-time
- Spanish
- Vital signs
- Computer literacy
- Paid holidays
- Disability insurance
Quick Apply
Clinical Studies Coordinator, Internal Medicine - Clinical
MD Anderson —Houston, TX
- $57,500 - $86,500 a year
- Full-time
- Hybrid work
- Customer service
- Internal Medicine
- Mid-level
- Health insurance
- Dental insurance
3d
Research Coordinator I - Internal Medicine, Critical Care (Bilingual)
UTHealth Houston —Houston, TX
- Full-time
- Spanish
- Internal Medicine
- HIPAA
- Health insurance
- Employee discount
Research Coordinator II - CAGT
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Vital signs
- Hospital
- Customer service
6d
Research Coordinator
IQVIA —Houston, TX
- $43,400 - $108,200 a year
- Full-time
- Nursing
- RN License
- 5 years
Research Nurse - Genitourinary Medical Oncology
MD Anderson —Houston, TX
- $77,500 - $116,500 a year
- Full-time
- Hybrid work
- CPR Certification
- Nursing
- RN License
- AD&D insurance
- Paid holidays
Training and Development Specialist VI (ICF)
Health & Human Services Comm —Houston, TX
- $6,760.12 - $7,652.91 a month
- Online Application
- Nursing
- Writing skills
- Microsoft Office
- Health insurance
- Opportunities for advancement
Quick Apply
3d
HIV Hybrid Medical Science Liaison
EVERSANA —Houston, TX
- $185,000 - $220,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Doctor of Philosophy
- Travel
Quick Apply
Occupational Health Manager
University of Houston —Houston, TX
- $88,400 - $101,700 a year
- Full-time
- Nursing
- RN License
- Bachelor of Science
Clinical Research Specialist (Neurology Department)
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Hospital
- Writing skills
- English
9d

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Clinical Nurse

IQVIA -
Houston, TX

Apply Now

Job Details

Full-time
$57,700 - $209,800 a year

Qualifications

RN License
BLS Certification
ACLS Certification

Full Job Description

Houston, United States of America | Full time | Office-based | R1536674

Job Summary

The Clinical Nurse must be knowledgeable of standard research and oncology care practices. The Clinical Nurse advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.

Essential Duties and Responsibilities

Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following:

Protocol Compliance

Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research.
Complies with NEXT Oncology SOPs
Participates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures
Collaborates with the PI, pharmacy, and other appropriate personnel to ensure proper use of and accountability for study drugs

Informed Consent

Identifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception)
Describes and abides by institutional policy and processes for informed consent
Assesses patient's understanding of the information provided during the informed consent process
Ensures timely re-consenting as needed by the physician investigator.
Confirms informed consent is obtained prior to performing any study specific tasks.

Management of Clinical Trial Patients

Provides complete patient assessment, including vital signs and pre-examination procedures
Gathers and assess objective and subjective data from the patient
Documents data and assessments accurately in the patient record
Assists the providers in all aspects of the consultation, treatment, procedures, and follow-up care
Records medical history and symptoms, completing documentation in the medical record
Coordinates patient care, acting as a liaison with other departments and organizations
Provides patient education before and after procedures, use of medical devices and equipment, and prescriptions
Triage of calls for urgent appointments, referrals for patient consults and resting, insurance precertification, and documentation
Educates the patient and family regarding clinical condition and/or disease process
Ensures timely completion of protocol-required events and other requirements (e.g. pharmacokinetics or-dynamics, scans, study visits, QOL.)
Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary
Evaluates patient's adherence to and documentation of self-administered protocol agents and the return of such agents
Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers
Evaluates patient's adherence to and documentation of self-administered protocol agents and return of such agents
Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers
Ensures appropriate communication between clinical and research staff related to patient-specific care needs
Ensures evidence-based symptom management as permitted by the protocol
Patient health counseling and instruction, including meeting with families and caregivers
Medication reconciliation, management, patient compliance, inventory, education
Ensures regulatory compliance with OSHA guidelines, CLIA regulations, HIPAA medical privacy guidelines

Documentation and Document Management

Documents all patient encounters in the legal medical record per licensure and institutional requirements
Obtains documents from outside providers or laboratories that are needed
Assesses documentation or discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents
Maintains the privacy and confidentiality of patient's source documents
Other duties as assigned

Required Education and Experience

Current BLS and ACLS or obtained within 90 days of employment
Current Registered Nursing License for the state the role is based in for RN's
Oncology experience preferred
Clinical trial experience preferred

Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $57,700.00 - $209,800.00. 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.

Where you'll work

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

nurse investigator jobs in houston, tx

Clinical Nurse

Nurse - Clinical Research Nurse

Sub Investigator (NP)

Registered Nurse

LTCR Nursing Facilities Senior Investigator

Research Nurse (Pedi Surgery)

LTCR HCS Nurse Surveyor

Research Nurse II-Part Time

Clinical Research Coordinator II - Neurology Alzheimer

Senior Administrative Assistant - Nursing Education

Clinical Research Assistant

Clinical Studies Coordinator, Internal Medicine - Clinical

Research Coordinator I - Internal Medicine, Critical Care (Bilingual)

Research Coordinator II - CAGT

Research Coordinator

Research Nurse - Genitourinary Medical Oncology

Training and Development Specialist VI (ICF)

HIV Hybrid Medical Science Liaison

Occupational Health Manager

Clinical Research Specialist (Neurology Department)

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