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Texas A&M University Health Science Center in Corpus Christi is seeking a Research Specialist I to support data-driven clinical research activities under general supervision. The role involves data and metadata compilation, projections, and day-to-day support for the PI and research staff.
The position requires a Bachelor's degree and four years of related experience. It also emphasizes HIPAA compliance, data management in EMR/EDC systems, and adherence to FDA, GCP, IRB requirements.
Research Specialist I
Texas A&M University Health Science Center
IBT - CGPM - Ramos
$3,750.00 monthly
Corpus Christi, Texas
Staff
Texas A&M University is committed to enriching the learning and working environment by promoting a culture that respects all perspectives, talents & lived experiences. Embracing varying opinions and perspectives strengthens our core values which are: Respect, Excellence, Leadership, Loyalty, Integrity, and Selfless Service.
As one of the fastest-growing academic health centers in the nation, Texas A&M Health encompasses five colleges and numerous centers and institutes working together to improve health through transformative education, innovative research and team-based health care delivery.
The Research Specialist I, under general supervision, compiles and reviews data and metadata. Computes projections and performs analysis and tests. Supports Principal Investigator and Research Personnel in the day-to-day conduct of clinical research activities.
Location: This position will report to IBT located in downtown Houston, Texas. The employee will be located at a Non TAMU private clinical office in Corpus Christi.
Schedule: May have to work on the weekends and/or after normal hours
Travel: May travel as required
Please note: This position is grant funded; future employment may be contingent upon future funding.
Compiles and reviews data and metadata.
Collects samples and measurements for experiments.
Implements and maintains data collection and summarization of clinical trials.
Computes projections.
Performs analysis and tests.
Makes and records observations and scientific measurements.
Assist with collection, processing, shipping, and tracking of research specimens.
Assist in preparing for sponsor monitoring visits, audits, and inspections.
Track enrollment, follow-up, and protocol compliance.
Maintain HIPAA compliance and participant confidentiality.
Screen potential participants for eligibility according to study protocols.
Schedule participant visits and study-related appointments.
Assist with participant recruitment and retention
Enter study data into electronic databases and EMRs.
Utilizes summarized results in scientific and/or clientele-oriented publications.
Prepares and writes proposals to funding agencies and maintains financial accounts related to research projects.
Prepare study materials and participant packets.
Maintain research records, regulatory binders, and study documentation.
Executes assigned protocols in accordance with research-governing entity requirements, including but not limited to Sponsor, FDA, and IRB requirements
Trains undergraduate and/or graduate students and other laboratory, technical or clinical staff involved in research.
Develops and maintains training materials for external users.
Monitors and tracks all lab-related supplies and inventory levels.
Purchases lab supplies, equipment, and services for the project.
Assists with Rural Oncology Grant invoice processing based on the sub-awardee needs.
Bachelor’s degree or equivalent combination of education and experience.
Four years of related experience in a specialized and relevant field of research.
Experience working in a physician practice, hospital, oncology clinic, or other healthcare environment
Experience with electronic data capture (EDC) systems and regulatory documentation
Current CITI Human Subjects Protection (HSP) training certification or equivalent, or the ability to obtain certification upon hire
Ability to multitask and work cooperatively with others.
Knowledge of word processing, spreadsheet, database, and presentation applications.
Interpersonal and communication skills.
Planning and organization skills.
Familiarity with appropriate laboratory and/or technical equipment.
Ability to effectively utilize a computer and applicable software.
Attention to detail.
Knowledge of FDA regulations, Good Clinical Practice (GCP), HIPAA, and human subject protections.
Proficient computer skills, including Microsoft Office Suite and electronic medical record (EMR) systems.
We are a prestigious university with strong traditions, Core Values, and a community of caring and collaboration.
Medical, prescription drug,dental,vision,life and AD&D,flexible spending accounts,and long-term disability insurancewith Texas A&M contributing to employee health and basic life premiums
12-15 daysof annual paid holidays
Up toeight hours of paid sick leaveand at leasteight hours of paid vacationeach month
Automatic enrollment in theTeacher Retirement System of Texas
Health and Wellness:Free exercise programs and release time
Professional Development: All employees have access to freeLinkedIn Learningtraining, webinars, and limited financial support to attend conferences, workshops, and more
Educational release time and tuition assistancefor completing a degree while a Texas A&M employee
Living Well,a program at Texas A&M that has been built by employees, for employees
All positions are security-sensitive. Applicants are subject to a criminal history investigation, and employment is contingent upon the institution’s verification of credentials and/or other information required by the institution’s procedures, including the completion of the criminal history check.
Equal Opportunity/Veterans/Disability Employer.