Total 2 science rd research job vacancies in 2200 william d tate grapevine tx 76051

Job Overview
Support study sites in the coordination of Phase I-IV clinical research studies, ensuring that studies are carried out according to protocol, standard operating procedures, GCP, and other applicable guidelines and regulations.

Essential Functions
• Coordinate clinical research studies conducted by a supervising principle investigator.
• Update and maintain skills, training and knowledge of current best nursing practice and topics related to clinical research.
• Safeguard the well-being of the subjects and ensure and maintain high standards:
• Maintain a safe environment in accordance with the Health and Safety policies
• Act as volunteer advocate
• Deal with volunteer and visitor concerns in a pro-active manner and taking remedial action as required
• Assist staff, both registered and unregistered in Nursing Practices and the delivery of care to the volunteer
• Report any deviation from normal practice to senior staff.
• Support study conduct by:
• Review of the study protocol, case report form (CRF), other study documents, and electronic data capture systems
• Participate in project meetings with the project team as needed
• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting up equipment and documents
• Plan logistical activity for procedures as per protocol
• Generate volunteer instructions
• Identify and obtain required supplies and equipment
• Prepare and deliver study specific training materials, documents, and records
• Troubleshoot study issues
• Participate in huddles to ensure daily tasks are assigned to team members are executed to the expected standards
• Assist with data quality checking and query resolution to ensure that data collected on study volunteers adhere to study protocol and ensuring quality control for content accuracy and completeness.
• Recruit and Screen volunteers for inclusion in study based on pre-determined criteria.
• Orientate volunteers to the study and the site including the purpose of the study, procedures and practical issues such as timelines for visits.
• Responsible for the correct administration and custody of study drug according to site standard operating procedures.
• Perform a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including phlebotomy, spirometry, vital signs, cannulation, and cardiac telemetry monitoring.
• Collect, record, and report clinical data and findings appropriately in case report forms (CRFs). Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
• Cooperate with study monitor and reserve sufficient time for questions during monitoring.

Qualifications
•
• 1 year relevant experience.
• r equivalent combination of education, training and experience.
• Good knowledge of clinical trials.
• In-depth knowledge of the principles of Good Clinical Practices (GCP).
• Good skill in using MS Windows and Office applications.
• Effective written and verbal communication skills including good command of the English language.
• Excellent interpersonal skills.
• Excellent problem-solving skills.
• Effective organizational skills.
• Ability to pay close attention to detail.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
•  Current active nursing license in the state, country, or region in which the site resides.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

***This position is NOT remote. Qualified candidates must be local to Saint Francis Health System or being open to relocation.

Job Summary: The Trauma Research Data Analyst will partner with trauma healthcare professionals to assist, develop and conduct novel and innovative clinical research studies aimed at advancing the field and improving care delivery and outcomes for trauma patients.  The role will assist in preparation of study protocols, study budgets, regulatory documentation, grant/funding applications, manuscript development as well as collect/retrieve and maintain data to assist with addressing study questions and evaluating study findings.  Also, will monitor study progress and resource utilization to ensure performance of study activities in accordance with study protocol, institutional policies and procedures, appropriate regulations, and good clinical practice.

Minimum Education: Bachelor’s degree in biology or any health sciences.  Master’s degree in public health, data/health science, health outcomes or similar field, preferred.

Licensure, Registration and/or Certification: None.

Work Experience: Minimum 3 years of experience in collecting and analyzing data. Publication experience, preferred. In lieu of work experience, a Master’s degree with a research background in a clinical setting will be considered.

Knowledge, Skills and Abilities: Excellent communication, presentation, interpersonal skills, both written and spoken with an ability to inform, influence, convince, and persuade a diverse team. Ability to work independently under the general guidance of the Research Manager for the common goals of the programs, as well as work with investigators in a multidisciplinary, dynamic, fast-paced and changing environment. Ability to manage and flex between multiple deadline-driven and ongoing projects while being solutions-oriented. Demonstrate a high degree of integrity, enthusiasm and initiative. Knowledge of healthcare, documentation, electronic medical health records, registry, health sciences clinical research, electronic medical health records and records management. Excellent project management, data utilization, complex problem solving, critical thinking, resource management and organizational skills with demonstrated success in leading projects and interacting with cross functional teams. Demonstrate strong computer skills especially in the utilization of Microsoft Word, Excel, and PowerPoint; ability to embrace new technologies.

Essential Functions and Responsibilities: Aid Trauma investigators and other stakeholders in generating novel research ideas and give input on study design and protocol development. Manage research studies/projects by collecting/retrieving, recording and maintaining accurate research data in a scientifically legible manner. Ensure scientific integrity of study design, implementation, and data collection to maintain scientific rigor and obtain high quality data. Conduct projects/studies independently under the guidance of Research Manager and Trauma physician investigator.

Assist interns/residents with trauma pilot projects and generate case reports/series. Assist statistician and other stakeholders in retrieving and maintaining relevant research data to address specific scientific questions. Assist Research Manager and Trauma physician investigator in PubMed literature search on relevant topics and present findings. Maintain timelines to ensure smooth progression to project/study completion to meet explicit pre-set deliverables. May conduct interviews with patients or their caregivers for potential observational studies (CITI training will be provided). Assist in data analysis, review, and data interpretation to generate high quality research findings for publications in peer-reviewed journals. Generate and draft reports, manuscripts, as well as graphs and charts to illustrate findings for presentations, manuscripts, grants, and other research-related activities. Assist Research Manager to generate regular assessment and status reports of the trauma program’s research and scholarly activities.

Decision Making: Independent judgment in making decisions from many diversified alternatives that are subject to general review in final stages only.

Working Relationships: Works with internal and/or external customers via telephone or fact to face interaction. . Works with internal and/or external customers via telephone or fact to face interaction.  Works with other healthcare professionals and staff.  Works frequently with individuals at Director level or above.

Special Job Dimensions: None.

Supplemental Information: This document generally describes the essential functions of the job and the physical demands required to perform the job.  This compilation of essential functions and physical demands is not all inclusive nor does it prohibit the assignment of additional duties.

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