quality assurance inspector

criminal investigator (special agent) - $40,000 recruitment incentive Jobs in Houston

dfr product implementation specialist Jobs in Houston

dfr product implementation specialist

elite field service technician Jobs in Houston

elite field service technician

evs technician

field investigator

National Investigative Training Academy

<div><p><b>Description</b></p>
<p>We are currently seeking motivated and driven individuals to join our team in surveillance/field investigation roles. No private investigator license is required&mdash;only a strong willingness to learn, develop new skills, and grow within a leading investigative firm.</p>
<p>
Immediate opportunities are available in the San Francisco, Oakland, Sacramento, and surrounding areas.</p>
<p>
If you are interested in building a career in this industry, we encourage you to contact us today and submit your resume.</p></div><p></p>

Field Investigator

Baylor College of Medicine

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Division of Critical Care Medicine with the Baylor College of Medicine and Texas Children's Hospital Department of Pediatrics is currently seeking a Research Coordinator III. This position coordinates activities of complex clinical research studies in Pediatric Critical Care Medicine. Primary responsibilities include patient enrollment, screening, monitoring of research participants, and reporting to the clinical research sponsor. Responsible for ensuring accurate data collection, documentation, organization and safety of study volunteers. Position requires prior clinical research experience and able to work independently with minimal oversight.. Experience with Pediatric Critical Care setting and studies is a plus.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Assists the investigator with the enrollment (recruiting, screening, and interviewing) and study consent process of patients into the Pediatric Critical Care Clinical Trial Studies.</li><li>
Explain the study&rsquo;s processes and procedures to educate the study participants.</li><li>
Responsible for assisting the Principle Investigator with collecting and recording study data related to catherization procedures, cardiac measurements, and related test and measurement for the study.</li><li>
Assist the Principle Investigator as necessary with electronic case reporting requirements in accordance with all FDA and clinical trial study requirements.</li><li>
Collects patient information; processes documents and enters information into a database.</li><li>
May perform research related procedures as required such as venipuncture (blood draws), EKGs/ECG&rsquo;s and obtain vital signs on study participants.</li><li>
Corresponds with patient throughout study.</li><li>
Interacts with sponsors and/or coordinating sites as required to facilitate protocol activities and maintains current study documents.</li><li>
Collects, processes and stores or ships blood or biological specimens as outlined per study protocols and associated lab or procedural manuals, in accordance with IATA Guidelines.</li><li>
Maintains records and regulatory documents and records for the research study.</li><li>
Schedules research participant for tests and procedures such as laboratory tests, x-rays, and other studies specific study visits for the research protocol.</li><li>
Retrieves and submits test results to the appropriate party.</li><li>
May assist with the supply orders and equipment necessary for the study.</li><li>
Assists in reviewing protocol documents, including abstracts, text, and informed consent for relevant information.</li><li>
Prepares documentation necessary to obtain initial and continued approval for the specific research protocol.</li><li>
Collaborates with physician, mid-level practitioners, and research nurses and data managers to document patient care.</li><li>
Conducts subject research study education as required within the scope of practice.</li><li>
Submits serious adverse event reporting and follow up as needed.</li><li>
Evaluates and analyzes clinical research data as appropriate.</li><li>
Performs other job duties as assigned.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.</li><li>
Two years of relevant experience.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2></div><div><ul><li>
Medical degree.</li><li><div>
At least three years of research experience.</div></li><li><div>
Ability to support occasional flexible work hours as needed by the study team.</div></li><li>
Pediatric Critical Care Medicine experience is a plus.</li></ul></div></div></div><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div><p></p>

Research Coordinator III - Pediatrics

Research Coordinator III - Pediatrics - Critical Care

Rheumatology Office Alex DeJesus, MD

<p><b>Clinical Research Coordinator </b></p><ul><li><b>Location Houston, Tx</b></li></ul><p><b>1 years of Experience required</b></p><p><b>Job Description </b></p><p><b>Clinical Research Coordinator (CRCs) </b></p><p>Clinical Research Coordinator will work in a team environment under the Leadership of the investigator with supervision of the Research Director or Team Lead.</p><p>Job Purpose: To promote good clinical practice in the conduct of clinical investigations. The Coordinator must possess an in depth knowledge of federal regulations to conduct clinical trials and protect human subject. One must be able to assure compliance with protocol and regulatory requirements, by collecting, recording and maintaining data and source documentation.</p><p><b>Participates in Subject Recruitment, Enrollment and Follow up Procedures </b></p><p><b>By: </b></p><ul><li>Integrating proposed clinical trial with current research activities</li><li>Attending and participating in investigator meetings</li><li>Listing and clarifying questions and concerns with the sponsor and investigator regarding enrollment goals sponsor expectations and study procedures</li><li>Monitoring enrollment goals and modifying recruitment plan as necessary</li><li>Maintaining patient screening/enrollment logs</li><li>Reviewing inclusion/exclusion criteria with investigator to assure subject eligibility</li><li>Reviewing and verifying source documents in subject&rsquo;s medical record to confirm subject&rsquo;s eligibility assuring that all screening, eligibility and enrollment procedures are performed</li><li>Reviewing the protocol, informed consent form and follow up procedure with potential study subjects</li><li>Conducting interviews at assess the subject&rsquo;s ability and willingness to follow and complete study procedures and visits</li><li>Obtaining informed consent from research subjects prior to any study related procedures and documenting appropriately</li><li>Following randomization procedures as per protocol</li><li>Dispensing study article as appropriate</li><li>Scheduling subject&rsquo;s follow up visits</li><li>Reviewing diaries and questionnaires completed by subjects</li><li>Ensuring appropriate specimen collection, batching and shipping as required</li><li>Assessing subject compliance with the test article and follow up visits</li></ul><p><b>Protects Subjects Confidentiality </b></p><p><b>By:</b></p><ul><li>Protecting patient privacy during initial and follow up interviews</li><li>Documenting protocol deviations and exemptions</li><li>Obtaining/reviewing original source documents</li><li>Abstracting data from medical records to clinic, consultation and referral notes to study forms and flow sheets</li><li>Recording accurate and timely data onto case report forms</li><li>Maintaining source documentation for all case report entries as applicable</li><li>Keying data for electronic submission</li><li>Transmitting data via fax, mail or electronically as requested</li><li>Correcting and editing case report form entries as appropriate</li><li>Resolving data queries</li><li>Completing and maintaining the study article dispensing log</li><li>Maintaining files of all study related documentation</li><li>Recognizing and reporting common laboratory values and alerts to investigator and sponsor</li></ul><p><b>Participates in Monitoring Visits and Audits </b></p><p><b>By</b>:</p><ul><li>Scheduling sponsor monitoring visits</li><li>Ensuring that EDC for Sponsor company is done within 3 business days and is correct</li><li>Collecting source documents for sponsor/audit review</li><li>Meeting with monitors/auditors during routine visits to discuss case report form completion, query resolution and other protocol related issues</li><li>Preparing for and participating in FDA inspections as needed</li></ul><p>Maintains Professional and Technical Knowledge</p><p>By:</p><ul><li>Attending educational workshops</li><li>Reviewing professional publications</li></ul><p>Job Type: Full-time</p><p>Pay: $37,941.00 - $55,091.00 per year</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Experience:</p><ul><li>Pharmaceutical research: 1 year (Required)</li></ul><p>Language:</p><ul><li> Fluent Spanish (Required)</li></ul><p>Ability to Commute:</p><ul><li>Houston, TX 77089 (Required)</li></ul><p>Work Location: In person</p>

Clinical Research Coordinator 1 yr. exp req.

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Department of Ophthalmology at Baylor College of Medicine is seeking a skilled and motivated Research Ophthalmic Technician to support clinical research initiatives under the guidance of the Principal Investigator. This role involves assisting with diagnostic testing, patient assessments, and data collection to advance research in ophthalmic science. The ideal candidate will work closely with both research and clinical teams, contributing to the success of ongoing studies and ensuring high-quality patient care and data integrity. This is a unique opportunity to be part of a dynamic research environment focused on improving vision health through innovation and discovery.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Enroll and schedule study participants for clinical research visits</li><li>
Collect detailed medical histories and maintain accurate records</li><li>
Operate ophthalmic diagnostic equipment (e.g., OCT, visual field, topography)</li><li>
Perform postoperative refractions and assist with patient assessments</li><li>
Support RxSight LAL patients with refractive targeting and light treatments</li><li>
Assist refractive surgery team weekly (scrub in or operate lasers)</li><li>
Perform other related duties as needed to support research and clinical teams</li><li>
Support clinical trials focused on ophthalmic diseases and surgical outcomes</li><li>
Maintain and calibrate specialized ophthalmic equipment used in research and patient care</li><li>
Assist faculty and residents during clinical procedures and research-related patient interactions</li><li>
Ensure compliance with study protocols, IRB regulations, and departmental standards</li><li>
Coordinate with multidisciplinary teams including optometrists, surgeons, and research staff</li><li>
Contribute to data collection, entry, and quality assurance for ophthalmology research studies</li><li>
Educate patients on study procedures and post-treatment care specific to ophthalmic interventions</li><li>
Performs other job related duties as assigned.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
High School diploma or GED.</li><li>
Two years of relevant experience.</li><li>
Certified Ophthalmic Assistant (COA), Certified Ophthalmic Technician (COT), Certified Ophthalmic Medical Technician (COMT).</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2></div><div><ul><li>
Strong refracting skills are preferred.</li></ul></div></div></div><p></p><p><b><br>
Work Authorization Requirement:</b></p><p><b>
This position is not eligible for visa sponsorship.</b> Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.</p><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div>

Technician, Research Ophthalmic

UTHealth Houston

<div><p>We are hiring a Research Coordinator II to join UTHealth McGovern Medical School, Department of Internal Medicine, Infectious Diseases in Houston, TX 77030. In this role, you will provide day-to-day project coordination for research studies (including industry-sponsored clinical trials and investigator-initiated studies). Clinical research will include participant screening, enrolment, consenting, visit conduct and scheduling; coordinating and collaborating with multiple team members and faculty; AE/SAE reporting; and writing research notes and searching through EMR. Bilingual in Spanish, preferred.</p><p><b>
What we do here changes the world.</b> UTHealth Houston is Texas&rsquo; resource for healthcare education, innovation, scientific discovery, and excellence in patient care. That&rsquo;s where you come in.</p><p><b>
Once you join us you won't want to leave.</b> It&rsquo;s because we reward our team for the excellent service they provide. Our total rewards package includes the benefits you&rsquo;d expect from a top healthcare organization (benefits, insurance, etc.), plus:</p><ul><li>
100% paid medical premiums for our full-time employees</li><li>
Generous time off (holidays, preventative leave day, both vacation and sick time &ndash; all of which equates to around 37-38 days per year)</li><li>
The longer you stay, the more vacation you&rsquo;ll accrue!</li><li>
Longevity Pay (Monthly payments after two years of service)</li><li>
Build your future with our awesome retirement/pension plan!</li></ul><p><b>
We take care of our employees!</b> As a world-renowned institution, our employees&rsquo; wellbeing is important to us. We offer work/life services such as...</p><ul><li>
Free financial and legal counseling</li><li>
Free mental health counseling services</li><li>
Gym membership discounts and access to wellness programs</li><li>
Other employee discounts including entertainment, car rentals, cell phones, etc.</li><li>
Resources for child and elder care</li><li>
Plus many more!</li></ul><p><b>
Position Summary:</b></p><p>
Under general supervision, assists with human subject research project conduct and management, including participant recruitment and data collection, entry, management, and analysis. Assists with research project logistics, maintaining records, preparing reports, and meeting research milestones and deadlines.</p><p><b>
Position Key Accountabilities:</b></p><ul><li>
Under general supervision, assist with human subjects research activities, including participant recruitment, informed consent, data collection through surveys, interviews, and observations, and ensuring that all activities are conducted according to study protocols.</li><li>
Maintains confidential records of collected data, ensures accuracy, compliance and integrity of data. Data may include human subject data and departmental programmatic data. Supports Data Management Sharing (DMS) plan.</li><li>
Prepares annual progress reports and applications for various committees and ensures that all staff have received the proper training/attended the appropriate training courses.</li><li>
Assists in the preparation of progress and annual reports, contracts and grant proposals to various funding agencies; works closely with the Office of Sponsored Projects on the submission of grants.</li><li>
May assist with regulatory submissions (i.e. Institutional Review Board(s), FDA, etc).</li><li>
Assists investigator with quantitative and qualitative data analysis, including statistical tests and the creation of figures, tables, and graphs. Helps prepare research papers, presentations, and reports including manuscripts for publications and conferences.</li><li>
Assists with the preparation of budgets and reviews re-budgeting needs and expenditures. Attends research-planning meetings to assist in preparing budget drafts for departmental leadership approval. Assists with invoicing.</li><li>
Responsible for coordinating and responding to site monitoring visits, audits, and inspections.</li><li>
May be responsible for maintaining study materials (i.e. test kits, investigational drugs and devices).</li><li>
May provide administrative direction training and guidance to study personnel within department.</li><li>
Performs other duties as assigned.</li></ul><p><b><br>
Certification/Skills:</b></p><ul><li>
Bilingual in English and Spanish, preferred.</li><li>
Working knowledge of MS Office Suite, preferred.</li><li>
Medical, therapeutic clinical trial, or similar experience, preferred.</li></ul><p><b>
Minimum Education:</b></p><ul><li>
Bachelor's Degree in a related field required May substitute required education with equivalent years of experience beyond the minimum experience requirement.</li></ul><p><b>
Minimum Experience:</b></p><ul><li>
2 years of relevant experience required May substitute required experience with equivalent years of education beyond the minimum education requirement.</li></ul><p><b>
Physical Requirements:</b></p><p>
Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects.</p><p><b>
Security Sensitive:</b></p><p>
This position is a security-sensitive position pursuant to Texas Education Code &sect;51.215 and Texas Government Code &sect;411.094. To the extent that a position requires the holder to research, work on, or have access to critical infrastructure as defined in Texas Business and Commerce Code &sect;117.001(2), the ability to maintain the security or integrity of the infrastructure is a minimum qualification to be hired for and to continue to be employed in that position. Personnel in such positions, and similarly situated state contractors, will be routinely reviewed to determine whether things such as criminal history or continuous connections to the government or political apparatus of a foreign adversary might prevent the applicant, employee, or contractor from being able to maintain the security or integrity of the infrastructure. A foreign adversary is a nation listed in 15 C.F.R. &sect;791.4.</p><p><b>
Residency Requirement:</b></p><p>
Employees must permanently reside and work in the State of Texas.</p></div>

Research Coordinator II - Internal Medicine, Infectious Diseases (Bilingual)

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Research Coordinator II is a position with responsibilities split between MEDDOS Clinical Trials and the Division of Cardiothoracic Surgery's faculty-led clinical outcomes research. The role focuses on development of academic presentations, abstracts, and manuscripts with coordination of literature review, preparation of publication-ready tables and figures, and submission to journals and scientific meetings. This role will also have oversight of screening, enrollment, and monitoring of research participants.</p><p></p><p><br>
The position works closely with faculty investigators, clinical research teams, statisticians, investigational pharmacies, sponsors, regulatory agencies and senior research staff to support timely and accurate dissemination of research findings. Success in this role requires comfort working closely with faculty and clinical teams, managing iterative revisions, motivating others to meet deadlines, and frequent collaboration with medical students and residents while maintaining high standards for accuracy, professionalism, and presentation. The Research Coordinator II operates with a high degree of independence across multiple concurrent projects.</p><p></p><p><br>
This role is designed for a Research Coordinator with a demonstrated aptitude for scientific communication and academic research support within a dual-function role. While a significant portion of the position focuses on analytical thinking, writing, organization, and collaboration to support scholarly work, the work with the MEDDoS Clinical trials component is actually the area that comprises the scientific communication and such and the division of cardiothoracic involves the direct patient care.</p><p></p><p><br>
The position primarily follows standard business hours, with flexibility to accommodate occasional early mornings, evenings, or weekend work as necessitated by study protocols.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Support outcomes research, clinical studies, and academic scholarship by assisting with scientific writing, publication development, and submission workflows.</li><li>
Prepare slide decks and visual materials for scientific meetings, invited talks, and internal presentations.</li><li>
Conduct structured literature searches (e.g., PubMed) to support manuscripts, abstracts, background sections, and presentations.</li><li>
Assist with drafting, editing, formatting, and finalizing scientific manuscripts, abstracts, and related materials in accordance with journal and conference requirements.</li><li>
Manage manuscript and abstract submissions through online portals (e.g., Editorial Manager, ScholarOne), including authorship documentation, file uploads, compliance checks, revision tracking, and correspondence.</li><li>
Collaborate with senior research staff to ensure consistency of terminology, formatting, and presentation style across publications.</li><li>
Enhance faculty productivity by managing time‑intensive scientific and administrative support tasks.</li><li>
Support the research mission by facilitating collaboration with BCM medical students and residents.</li><li>
Coordinate day‑to‑day activities of research protocols, including screening, enrollment, consent, monitoring, and follow‑up of research participants.</li><li>
Interview, screen, and obtain informed consent from study participants; explain study processes and procedures to educate participants regarding research protocols.</li><li>
Schedule research participants for protocol‑required tests and procedures, including laboratory tests, imaging, surgeries, and other study‑specific activities.</li><li>
Attend surgical procedures as required by the study protocol.</li><li>
Collect, document, and manage clinical and research data in accordance with study protocols; ensure timely completion of Case Report Forms (CRFs) and accurate entry into Electronic Data Capture (EDC) systems.</li><li>
Retrieve, review, and submit test results to appropriate internal and external parties.</li><li>
Ensure accurate data collection, documentation, organization, and protection of the safety and confidentiality of research participants.</li><li>
Establish, organize, and maintain regulatory binders, source documents, study files, and other study‑specific materials.</li><li>
Assist the Principal Investigator (PI) and Regulatory staff with the preparation, review, tracking, and submission of documents to the Institutional Review Board (IRB).</li><li>
Work closely with the PI and Regulatory staff to ensure compliance with all regulatory, institutional, and study‑specific requirements, including IRB approvals, education requirements, conflict of interest disclosures, participant and staff safety protections, and financial terms and conditions.</li><li>
Assist the PI with submission of event reports, including non‑compliance, adverse events, and unanticipated problems.</li><li>
Track protocol amendments, clarification letters, and study updates; implement changes accordingly.</li><li>
Collect, process, ship, and maintain documentation for biological specimens in accordance with study protocols.</li><li>
Maintain adequate inventory of study supplies.</li><li>
Manage investigational drug or device accountability in compliance with sponsor protocols and institutional policies, when applicable.</li><li>
Coordinate participant payments in accordance with BCM and site‑affiliated policies and procedures.</li><li>
Perform billing reconciliation in EPIC for research‑related procedures billed to the study.</li><li>
Attend investigator meetings as required or requested by the PI and/or sponsor.</li><li>
Performs other job duties as assigned.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.</li><li>
One year of relevant experience.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2></div><div><ul><li>
Master&rsquo;s degree preferred.</li><li>
Strong written and verbal communication skills with high attention to detail.</li><li>
Demonstrated ability to manage multiple projects and meet deadlines.</li><li>
Experience with scientific writing, abstract or manuscript preparation, and medical literature review.</li><li>
Familiarity with an academic medical setting.</li><li>
Familiarity with aortic surgery, cardiovascular research, or related surgical subspecialties.</li><li>
Proficiency with Microsoft Word, PowerPoint, and Excel.</li><li>
Experience with REDCap, EPIC, Medidata, and/or Oracle preferred.</li><li>
Familiarity with reference management tools (e.g., EndNote, Zotero, Mendeley) preferred.</li><li>
Strong problem‑solving skills, initiative, and professionalism when working with faculty, clinical teams, and external collaborators.</li></ul></div></div></div><p></p><p><b><br>
Work Authorization Requirement:</b></p><p><b>
This position is not eligible for visa sponsorship.</b> Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.</p><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div>

Research Coordinator II (Scientific Writing & Presentations) - Surgery

Explore 280+ Field investigator in Houston this April. Find roles across top companies and apply now to boost your career.