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Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. Preferred Skills:Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).

<div>Clinical Trial Research Assistant The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic/Onsite </div><div>Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. This is an exciting opportunity to be involved in cutting-edge medical research in a supportive and dynamic outpatient setting. </div><div>Key Responsibilities:</div><ul><li>Process and ship biological specimens per study protocol.</li><li>Maintain lab inventory and order clinical trial supplies.</li><li>Ensure accurate and complete study documentation in compliance with institutional and federal regulations.</li><li>Support research coordinators with testing procedures and overall trial conduct.</li><li>Advertise, screen, recruit, and enroll patients in clinical trials.</li><li>Obtain informed consent and explain study participation clearly.</li><li>Schedule appointments, diagnostic tests, and study-related procedures.</li><li>Assist with data entry into electronic case report forms (eCRFs) and databases.</li><li>Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB).</li><li>Maintain knowledge of current study protocols and standard operating procedures.</li><li>Prepare for monitoring visits, sponsor audits, and regulatory inspections.</li><li>Help collect and report adverse events.</li><li>Attend ongoing training and continuing education relevant to research duties.</li></ul><div> </div><div>Preferred Skills:</div><ul><li>Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).</li><li>Experience with specimen processing, shipping, and documentation.</li><li>Bilingual (English/Spanish) is a plus.</li></ul><div> </div><div>Requirements:</div><ul><li>Bachelor’s degree or higher in a science-related field** US University ** (e.g., biology, chemistry, biochemistry).</li><li>Previous lab experience with biological specimen handling.</li><li>Proficient in maintaining documentation and adhering to study protocols.</li><li>MUST live within 30 mins of The Woodlands.</li><li>THIS POSITION IS ONSITE.</li><li>Must be Technologically Adept.</li><li>Strong attention to detail and protocol compliance.</li><li>Excellent communication and organizational skills.</li></ul><div> </div><div>Why Join Us?</div><ul><li>Supportive, collaborative team environment.</li><li>Opportunity to work on innovative, impactful clinical trials.</li><li>On-the-job training and professional development.</li><li>Regular weekday schedule with no night or weekend shifts.</li></ul>

Advanced Rheumatology of Houston

Clinical Trial Research Assistant

Adverse Events

Biochemistry

Biological Processes

Biology

Calendar Management

Case Report Form (CRF)

Chemistry

Clinical Assessment

Clinical Research

Clinical Trial

Communication Skills

Data Entry

Detail Oriented

Documentation

Electrocardiogram

English Language

FDA (Food and Drug Administration)

Federal Laws and Regulations

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

Informed Consent

Inventory Management

Laboratory

Medical Products

Medical Research

Multilingual

Order Supplies

Organizational Skills

Outpatient Care

Phlebotomy

Regulations

Regulatory Reports

Research Protocols

Sample/Specimen Processing

Shipping Documents

Spanish Language

Standard Operating Procedures (SOP)

Team Player

Testing

Betterteam

In addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period: Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire. This position will be responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures.

HOUR

Overview:
Retina Consultants of Texas (RCTX) is seeking a Research Assistant  to join our innovative team with the mission of Fighting Blindness For The World To See. This position will be responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time. This position will be based at The Woodlands Clinic. Candidates must be able to meet the needs of the patients and providers, and support the Research Department hours of 6:30am-5pm Monday through Friday. Schedules are provided weekly and are based on the provider's clinic, patient and surgery schedules.  Retina Consultants of Texas is the largest and most respected retina-only ophthalmology practice in the United States. Our group consists of 26 world renowned physicians leading the world in retinal care. While serving two major metropolitan markets (and their extensions) our combined culture allows us to best serve our patients, referral sources and our own team of physicians. RCTX also invests heavily in diagnostic equipment, providing state-of-the-art retina imaging, laser and diagnostic capabilities to each patient. This, combined with the clinical expertise of our physicians, an outstanding and devoted staff, and 25 convenient locations to serve our patients. We worked hard to create our culture as Retina Warriors. We strongly emphasize our core values of Hard Work, Authentic Care and Innovation in everything we do. It is our belief that by investing in our people, our people will be empowered of their own accord to provide the highest quality patient experience. In addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period: <ul><li>Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire.</li><li>Employer Paid Benefits such as long-term disability, $25,000 basic life insurance policy, 3% 401(k) safe harbor contribution, HSA employer contributions, annual performance merit increases, certification opportunities, rewards & recognition platform, WellHub Starter Plan Gym Membership, paid time off and (8) paid holidays + (1) floating holiday annually.  </li></ul>Starting Pay Rate is $19.00 per hour and eligible for overtime. RCTX is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, age, national origin, disability, military service, veteran status, genetic information, or any other protected class under applicable law.

Responsibilities:
<ul><li>Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines. </li><li>Prepare visit-specific documentation and charts for Clinical Research Coordinator</li><li>Inform subjects and obtain written consent in regard to ICF’s </li><li>Assist Coordinator in patient care and management</li><li>Assist Coordinator in monitoring subject flow and assist in subject care and management</li><li>Accurately collect and record all necessary data (e.g. demographics, medical history, adverse events, concomitant medications, etc.) during study visit</li><li>Transcribe subject study information from source documents to the Electronic Case Report Forms</li><li>Administer all mandatory questionnaires to study subjects</li><li>Set up, prepare subject, and conduct electrocardiograms on subject who require ECG per study protocol</li><li>Scribe ocular exams for doctors and confirm appropriate treatment per protocol</li><li>Promptly request all necessary medical records for Serious Adverse Event Reporting</li><li>Collection, processing, and shipment of laboratory biological samples for analysis</li><li>Perform intraocular pressure checks post-injections</li><li>Review and resolve data management queries as needed</li><li>Trial frame refraction and ETDRS visual acuity testing</li><li>Other duties as assigned </li></ul>

Qualifications:
Skills/Competencies: <ul><li>Biliginual preferred </li><li>Ability to multitask</li><li>Computer efficient </li><li>Commnucates well both verbally and electronically; email, MS Teams, etc. </li><li>Detail oriented </li></ul>Education Requirements<ul><li>Bachelors degree or 4 years of ophthalmic experience in lieu of degree</li></ul> Experience Requirements:<ul><li>No experience required with a Bachelors degree otherwise at least 4 years of ophthalmic experience </li></ul>

Retina Consultants of Texas

Clinical Research Assistant

Analysis Skills

Clinical Study Publications

Data Management

GCP (Good Clinical Practices)

ICH Regulations

Injections

Medical Records

Medications

Multitasking

Ophthalmology

Patient Care

Record Keeping

Specimens/Samples

[AW]-iCims

ADAPTED_NOW

Nature & Purpose of Position/Usual Duties: HIDTA Intelligence Analyst I, II & III : Conducts extensive research and multi-faceted inquiries that involves locating and identifying subjects, vehicles, evidence, and assets using numerous law enforcement networks and commercial databases. Primary Responsibilities (Staff Positions Only): HIDTA Intelligence Analyst I: Duties performed will vary with the particular program, project, or area of expertise.

Requisition: 202500242S Occupational Category (Staff Positions Only): Technical/Para-Professional Hiring Salary: Monthly-Staff Department: High Intensity Drug Trafficking Areas (HIDTA) General Requirements: HIDTA Intelligence Analyst I: Bachelor’s degree in Criminal Justice or a related field. Experience in a law enforcement or analytical field needed or advanced course work, internship, and/or research in specialized law enforcement area preferred. Additional experience may be considered in lieu of education. HIDTA Intelligence Analyst II: Bachelor’s degree in Criminal Justice or related field. Three years’ experience in a law enforcement agency or analytical field. A combination of education, experience, and training that would produce the required knowledge and abilities will be considered. HIDTA Intelligence Analyst III : Bachelor’s degree in Criminal Justice or related field. Five years’ experience in a law enforcement agency or analytical field. A combination of education, experience, and training that would produce the required knowledge and abilities will be considered. Nature & Purpose of Position/Usual Duties: HIDTA Intelligence Analyst I, II & III : Conducts extensive research and multi-faceted inquiries that involves locating and identifying subjects, vehicles, evidence, and assets using numerous law enforcement networks and commercial databases. Establishes and maintains contact with counterparts in other intelligence organizations to eliminate duplication, enhance professional development, and keep abreast of current trends. Primary Responsibilities (Staff Positions Only): HIDTA Intelligence Analyst I: Duties performed will vary with the particular program, project, or area of expertise. Performs research using law enforcement and commercial databases, organizes and summarizes vast amounts of data. Prepares written reports and biographical datasheets, and prepares subpoenas. Organizes and disseminates subscriber and toll information, conducts telephone analysis, prepares graphs, charts, PowerPoint presentations and other visual aids. Ability to perform data input regarding subjects, vehicles and telephone subscriber information into criminal databases and investigative software. Performs other related duties as assigned. HIDTA Intelligence Analyst II: Performs research using law enforcement and commercial databases. Organizes and summarizes vast amounts of data and prepares written reports and biographical data sheets. Prepares subpoenas, organizes, and disseminates subscriber and toll information. Conducts telephone analysis. Prepares graphs, charts, PowerPoint presentations and other visual aids. Creates and gives professional presentations. Performs data input regarding subjects, vehicles and telephone subscriber information into criminal databases and investigative software. Performs other related duties as assigned. HIDTA Intelligence Analyst III : Performs advanced research using law enforcement and commercial databases. Organizes and summarizes vast amounts of data and prepares written reports and biographical data sheets. Prepares subpoenas, organizes, and disseminates subscriber and toll information. Conducts telephone analysis. Prepares graphs, charts, PowerPoint presentations and other visual aids. Creates and gives professional presentations. Performs data input regarding subjects, vehicles and telephone subscriber information into criminal databases and investigative software. Performs other related duties as assigned.

Sam Houston State University

HIDTA Intelligence Analyst I, II,or III (full-time, temporary) - 2 positions to be filled

Luxottica

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Clinical Trial Research AssistantAdvanced Rheumatology of Houston

Clinical Research AssistantRetina Consultants of Texas

HIDTA Intelligence Analyst I, II,or III (full-time, temporary) - 2 positions to be filledSam Houston State University

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