Clinical Research Coordinator III (RN)
$43.68k - $73.92kAmerican Oncology Partners, PA
Location: Oncology Consultants - Memorial City Hiring Range: $43,680.00 - $73,920.00 Position Summary The Clinical Research Coordinator functions as an integral part of the Research Team in clinical trial management at Oncology Consultants. The Clinical Research Coordinator is involved in multiple aspects of the research process under the general supervision of the Clinical Research Manager and the Research Director. Key Performance Areas KPA 1 – Study Start-Up, Regulatory & Site Initiation Responsible for supporting study feasibility, regulatory submissions, and study initiation activities to ensure compliance with protocols, regulatory requirements, and institutional policies. Applies knowledge of study design to evaluate protocol feasibility at the site. Assists Regulatory staff in preparing and submitting documents to Institutional Review Board (IRB). Participates in study site initiation activities. Attends and participates in investigator meetings and clinical trial conferences as directed. Documents protocol deviations and exemptions. Prepares for and participates in FDA inspections. Communicates effectively with IRBs, sponsors, investigators, and research team members. KPA 2 – Patient Recruitment, Screening & Enrollment Responsible for patient recruitment, screening, eligibility verification, and enrollment activities in accordance with study protocols. Participates in subject/patient recruitment and evaluation of eligibility. Reviews and verifies required source documents to confirm study eligibility. Reviews inclusion/exclusion criteria with investigator to assure subject eligibility. Conducts interviews to assess subject ability and willingness to complete study procedures. Maintains patient screening and enrollment logs. Reviews protocol requirements, informed consent, and follow-up procedures with potential study subjects. Follows randomization procedures per protocol. Demonstrates commitment to superior customer service and patient-centered communication. KPA 3 – Clinical Trial Coordination & Patient Care Activities Responsible for coordinating study visits, performing clinical procedures, and ensuring protocol compliance throughout the research process. Ensures study drugs are dispensed per protocol and maintains drug accountability records. Reviews returned drugs for compliance and documents findings. Provides direct care in study compliance throughout the research experience. Performs peripheral venipuncture per organizational standards. Ensures proper specimen collection, batching, processing, and shipping per protocol. Works collaboratively with site staff to process specimens. Prepares and ships study-required specimens per protocol manual. Obtains test results and reports to the physician investigator. Attends clinic visits with the investigator and assists in following study guidelines. KPA 4 – Data Management, Documentation & Monitoring Support Responsible for maintaining accurate study documentation, source documentation, and supporting sponsor monitoring and audit activities. Obtains and reviews original source documents (recordings, scans, test results, procedure reports). Abstracts data from medical records and other documentation to study forms and flow sheets. Completes and maintains study documentation and case report forms. Resolves data queries. Schedules sponsor monitoring visits. Prepares case report forms and source documents for sponsor and audit review. Assists with audit preparation and monitoring visits. KPA 5 – Research Program Support, Education & Administrative Support Responsible for supporting research department operations, education, budgeting support, and departmental coordination activities. Participates in educational and training activities and continuing education. Supports and assists management team with department projects. Assists in maintenance of budgetary data for each clinical trial. Assists in planning department coverage for clinic visits, data management, and meetings. Maintains professional communication with internal and external customers. Demonstrates strong verbal and written communication skills. Position Qualifications Education Degree in the life sciences or health sciences such as Registered Nurse (R.N.), Doctor in Philosophy (Ph.D.), Medical Doctorate (M.D.), or other related degree. Minimum Relevant Experience 2 or more years of clinical research experience. Certifications/Licenses Continuing education participation is expected, and research certification through a recognized national organization (SOCRA, ACRP) is encouraged. NIH protection of Human subjects online course will be required annually. IATA training will be required every 2 years. Travel 0 - 25% American Oncology Network AON is an alliance of physicians and veteran healthcare leaders dedicated to ensuring the long-term success and viability of oncology diagnosis and treatment in community-based settings. It is the fastest growing national network of community oncology practices delivering local access to exceptional cancer care. AON serves its expanding network of partner practices by providing proven practice management expertise. Our employees across the country work together to empower physicians to make cancer care better. By driving integrated, collaborative care, we are proudly helping community oncologists deliver the highest quality care to every patient. Cancer touches everyone. Being able to make a difference in the lives of those fighting this disease is something our employees at AON cherish and never take for granted. A career in oncology offers all sorts of rewards. But working at AON offers employees more than most. As a fast-growing national company, the opportunity to join a national workforce with flexible work options is available. We offer competitive compensation packages that include comprehensive health insurance with a robust provider network. Our 401k, which offers a 100% match and investment options, is available to full-time and part-time staff members, and we feature a generous Paid Time Off (PTO) program. At AON, we offer you more than a job, we offer you a career. As a network of independent oncology practices working together as one, we host annual summits each year, providing our employees a chance to collaborate with AON peers from across the country. Promoting from within is a priority at AON, and we support our team members continued growth through professional development programs and tuition assistance. #J-18808-Ljbffr American Oncology Partners, PA
$43.68k - $73.92k
Clinical Research Coordinator III (RN)### Clinical Research Coordinator III (RN)Apply: US-TX-Houston: Full time: Posted Yesterday: JR7643**Location:**Oncology Consultants - Memorial City**Hiring Range:**$43,680.00 - $73,920.00# **Position Summary**The Clinical Research...SuggestedFull time- Oncology Consultants in Houston, TX seeks a Clinical Research Coordinator III (RN) to support pharmaceutical trials across start-up, recruitment, care, data management and audits at Oncology Consultants - Memorial City. The role reports to the Clinical Research Manager...SuggestedFull time
- Oncology Consultants in Houston, TX seeks an experienced Clinical Research Coordinator III (RN) to join our research team. The role supports study start-up, regulatory submissions, patient recruitment, and data management under the supervision of the Research Director....Suggested
- Baylor College of Medicine is seeking a Research Coordinator III to provide centralized coordination support within the Office of Research (OCR... ...across the College and affiliates. This onsite role supports clinical trial activities in drug and device trials, coordinating...SuggestedWork at office
- Houston Methodist is seeking a Research Coordinator III to manage multiple clinical research projects and Principal Investigators, collecting patient data per study protocol and handling general administrative duties to support the study. The role evaluates results, summarizes...Suggested
- ...Charge RN III Outpatient Services At Houston Methodist, the RN... ...Proficient stage of Benner's model of clinical practice. This position... ...unit and hospital staff and coordinating unit and hospital-wide... ...leader in innovative medical research with a comprehensive residency...Permanent employmentShift work
- ...Description Position: Clinical Research Coordinator II Purpose: The purpose of the Clinical Research Coordinator II role is to ensure the successful execution of multiple concurrent clinical trials through effective study coordination, subject management, and...Work experience placement
$55k - $85k
...Clinical Research Coordinator IHouston, Texas, United StatesCare Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly...Weekly payFull timeTemporary workWork at officeLocal areaWorldwideFlexible hours- ...Clinical Research Coordinator IILocation: Houston, TX area.Employer type: Acute care.What the work involves:EDUCATION Bachelor's degreeEXPERIENCE Four years of research experiencePreferred CCRC - Certified Clinical Research Coordinator (ACRP) or CCRP - Certified Clinical...
- Harris Health en Houston busca una Enfermera Registrada de nivel II/III para la Gastroenterología y Hepatología Pediátricas, colaborando... ...os con enfermedades GI/hepáticas complejas. Se requiere licencia RN de Texas o NLC, BLS; ACLS es preferible. El puesto implica triage...
$41.82 - $53.81 per hour
RN II/III - Pediatría GI Multiespecializada (TMC) Aplicar Enfermero/a registrado/a pediátrico/a - Clínica de GI/Hígado PediátricaÚnase a un equipo colaborativo de Gastroenterología/Hepatología Pediátrica dedicado a la atención de niños con enfermedades gastrointestinales...$60k - $72k
...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Clinical Research Coordinator Clinical Ops - Houston Full Time Houston, TX, US Salary Range: $60,000.00 To $72,000.00 Annually About Us At Empathx, we...Full timeWork at officeMonday to Friday- UTHealth Houston seeks a Research Coordinator II to support hematology clinical trials at the McGovern Medical School in Houston, TX. Responsibilities include screening, scheduling, enrolling participants, data collection, and entry into the electronic capture system,...
- DM Clinical Research is seeking a Clinical Research Coordinator II for psychiatry to ensure quality data and adherence to sponsor protocols and regulatory standards at assigned investigative sites in the United States. The role emphasizes enrollment targets, training completion...
- UTHealth Houston is seeking a Research Coordinator I to support neurodegenerative/neuromuscular clinical trials. You will assist with participant recruitment, data collection, and study logistics to ensure timely and compliant trial execution. The role involves coordinating...
- Alliance Clinical Network in Houston, TX seeks a Clinical Research Coordinator I to oversee participant visits, data collection, and study compliance under GCP guidelines. You will work with the PI, manage screenings, informed consent, IP accountability, and entry of data...
- ...N Loop W,Suite 250,Houston, TX, 77008,United States Employee Type PRN Please note that this position is PRN! Job Title: Clinical Research Coordinator II FSLA Classification: Non-Exempt Reports to: Site Operations Manager Job Summary/ Objective: The Clinical Research Coordinator...ReliefWork at officeMonday to Friday
- Lumi Research is seeking an Oncology Clinical Research Coordinator II to oversee regulatory and patient consenting for clinical trials, ensuring data accuracy and compliant documentation. This role involves training new team members, coordinating study visits, and maintaining...
- Jimmy Jazz is seeking a Clinical Research Coordinator II for a PRN role at our Houston, TX site. The incumbent will support management and oversight of clinical trials under the Site Operations Manager, ensuring documentation and regulatory compliance while coordinating...Relief
- DM Clinical Research Group is seeking a Clinical Research Coordinator II - Psychiatry in the Bellaire/Houston area. You will ensure quality data per sponsor protocol, FDA regulations, and ICH/GCP guidelines, with a focus on achieving enrollment targets and coordinating...
- Houston Methodist seeks a Research Coordinator to manage day-to-day activities of clinical research protocols, screen patients for eligibility, and ensure accurate data collection and documentation while maintaining participant safety. The role collaborates with research...
- The Clinical Research Coordinator II - Psychiatry will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The...
- Empathx in Houston is seeking a Clinical Research Coordinator to manage the day-to-day coordination of studies across Phase I-IV, with a primary focus on psychiatry and CNS. Based on site in Houston, the CRC serves as the main contact for study participants and ensures...Full time
- CrofootMD Clinic and Research Center in Houston, TX is seeking an experienced Certified Clinical Research Coordinator (CCRC/CCRP) to join the Clinical Research Department on-site. The role focuses on HIV and infectious disease trials, requiring independent study coordination...
- Oncology Consultants is seeking a Clinical Research Coordinator to join the Research Team in Houston, supporting trial management under the Clinical Research Manager and Research Director. The role involves study start-up, regulatory compliance, patient recruitment, and...
- Certified Clinical Research Coordinator (CCRC/CCRP) Position Type: Full-Time Location: Houston, Texas | On-Site Department: Clinical Research Reports To: Director of Research Position Overview CrofootMD Clinic and Research Center is seeking an experienced, nationally certified...Full timeWork at officeWeekend workAfternoon shiftEarly shift
- Houston Methodist is seeking a Research Coordinator II to oversee daily activities of research protocols, ensure accurate data collection, and... ...Under minimal supervision, you will gather patient data for clinical studies and perform general administrative duties supporting...Full time
- UT Health is seeking a Research Coordinator to support Huntington's disease clinical trials. The role involves patient recruitment, screening, scheduling, visit coordination, and data management to ensure timely study execution and protocol compliance. Preferred candidates...Full time
- The Menninger Clinic in Houston, TX seeks a Research Coordinator to support and oversee multiple clinical research studies across inpatient and outpatient units. This role involves direct patient interaction, coordination with academic partners, and regulatory responsibilities...
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