Research Scientist II

The University of Texas at Dallas

Richardson (TX)

Hybrid

USD 90,000 - 130,000

Full time

4 days ago

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Benefits offered by this job

Internal Training

BCBS PPO Medical insurance - 100% paid

PPO and DHMO Dental Insurance Plan

Long and short-term disability

TRS Retirement Plan

Voluntary Retirement Plans

Paid time off

Paid Holidays

Paid Winter Break

Fertility Benefits

Remote Work Options

Job summary

The University of Texas at Dallas' Texas Biomedical Device Center seeks a Research Scientist II to help lead clinical trials in regulatory-compliant environments. You will supervise staff and coordinate studies under the Chief Medical Officer.

Candidates should have a PhD and 2+ years in neuroscience or biomedical engineering with FDA regulatory experience; strong communication and project management skills are essential.

Qualifications

PhD in a field related to research and at least 2 years of relevant experience.
Strong background in neuroscience or biomedical engineering with expertise in regulatory affairs and clinical research.
Experience with regulatory management for investigational neuromodulation or active implantable devices.

Responsibilities

Lead and supervise research personnel and coordinate project results.
Manage FDA, IRB, and DSMC regulatory activities for multiple investigational neuromodulation device studies.
Develop regulatory strategy for multi-site investigational studies, ensuring compliance with US regulations, standards, and guidance.
Prepare and submit IDEs, annual reports, protocol amendments, continuing reviews, and safety notifications.
Provide regulatory-centric education and training to staff, investigators, and students.
Stay current on regulatory trends and improve TxBDC processes and procedures.

Skills

Regulatory affairs

Clinical research

GCP/IRB/DSMC

FDA filings

Regulatory strategy

Multi-site studies

Project management

Education

PhD in neuroscience/biomedical engineering

Job description

The Texas Biomedical Device Center (TxBDC) supports active projects in vagus nerve stimulation, recovery from neurological injuries, and implantable neural devices. The Research Scientist II will help lead TxBDC clinical trials by supporting scientific progress within the framework of FDA regulations. They may also be asked to develop and provide regulatory-centric education and training to TxBDC staff, investigators and students. This position reports to the Chief Medical Officer within TxBDC. The Research Scientist will provide direction and supervision to units engaged in research, investigation or other technical operations as well as perform research for the university.

Minimum Education and Experience

A minimum of a PhD in a field directly related to research and a minimum of two years of experience/expertise as noted below.

Preferred Education and Experience

The successful candidate will have a strong background in neuroscience, biomedical engineering, or a related field, with expertise in regulatory affairs, clinical research, and neurorehabilitation.

Strong working knowledge of Good Clinical Practice ( GCP ), IRB and DSMC management, and clinical trial compliance.
Experience independently authoring, submitting, and maintaining FDA regulatory filings for clinical studies.
Demonstrated experience translating regulatory strategy into compliant implementation for study and site changes.
Excellent written and verbal communication, organizational, and time management skills. Project Management experience in a clinical research environment.
Direct experience with regulatory management for investigational neuromodulation or active implantable devices.

Other Qualifications

To the extent this position requires the holder to research, work on, or have access to critical infrastructure as defined in Section 117.001(2) of the Texas Business and Commerce Code, the ability to maintain the security or integrity of the critical infrastructure is a minimum qualification to be hired and to continue to be employed in the position.

Essential Duties and Responsibilities

Perform all duties related to specified research which may include:

Supervise and instruct key research personnel in work; coordinate and review the work of assigned research staff; submit project results to director and prepare and assist in the preparation of scientific papers.
Manage FDA , IRB , and DSMC regulatory activities for multiple investigational neuromodulation device studies, including Early Feasibility and Pivotal IDE trials.
Develop and implement regulatory strategy for multi-site investigational device studies, ensuring compliance with US regulations, standards, and guidance.
Assess the regulatory impact of study and site changes, and guide teams through compliant implementation.
Prepare and submit IDE trial submissions, annual reports, protocol amendments, continuing reviews, and safety notifications.
Conduct periodic, routine audits of TxBDC clinical studies to assess compliance with GCP , study protocols, and applicable federal and state policies.
Manage study deviations and corrective action plans (CAPAs), and coordinate study team responses to external monitoring findings.
Develop and provide regulatory-centric education and training to TxBDC staff, investigators, and students.
Collaborate with study teams, oversight bodies, and external partners to ensure compliant and efficient study execution.
Stay current on national regulatory trends and best practices, and apply this knowledge to improve TxBDC’s regulatory processes and procedures.

Physical Demands and Working Conditions

Laboratory environment with walking/standing/sitting throughout the day. Office environment, requiring sitting at a computer for extensive time.

Physical Activities

Working Conditions

Additional Information

Internal candidates may be given preference

After the probationary period, this role may be eligible for a hybrid (partly remote/partly in office) work schedule, subject to business need and manager approval. May be required to use personal computer and other standard office equipment. Must be located within the DFW Area and have the ability to be on campus with 24 hours of notice. A UT Dallas Remote Work Agreement will be required within 14 days after approval.

What We Can Offer

UT Dallas is an Equal Opportunity Employer with an employee-friendly and supportive work environment. Our comprehensive compensation and benefits package that is effective as of your hire date includes:

Internal Training
BCBS PPO Medical insurance - 100% paid for full-time employees
PPO and DHMO Dental Insurance Plan - PPO plans include ortho benefits
Long and short-term disability
TRS Retirement Plan - defined benefit plan offering lifetime annuity upon retirement
Voluntary Retirement Plan Options - additional savings opportunities with Tax-Sheltered Annuity Plans and Deferred Compensation Plans
Paid time off
Paid Holidays
Paid Winter Break
Fertility Benefits
Remote Work Options - approved by department

All UT Dallas employees have access to various professional development opportunities, including a membership to Academic Impressions, LinkedIn Learning, and UT Dallas Bright Leaders Program.

Special Instructions Summary

1) All employees serve as a representative of the University and are expected to display respect, civility, professional courtesy, consideration of others and discretion in all interactions with members of the UT Dallas community and the general public.

2) The University of Texas at Dallas is committed to providing an educational, living, and working environment that is welcoming, respectful, and inclusive of all members of the university community. UT Dallas does not discriminate on the basis of race, color, religion, sex (including pregnancy), sexual orientation, gender identity, gender expression, age, national origin, disability, genetic information, or veteran status in its services, programs, employment, and education, including in admission and enrollment. The University is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities. To request reasonable accommodation in the employment application and interview process, contact the ADA Coordinator. For inquiries regarding nondiscrimination policies, contact the Title IX Coordinator.

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