Top 62 Clinical research coordinator Jobs in Round Rock Tx

Clinical Research Associate I
Dell Medical School —Austin, TX
- From $40,000 a year
- Overtime
- Nursing
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Clinical Research Coordinator
Dermatologists of Central States —Pflugerville, TX
- Nursing
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Pinnacle Clinical Research —Austin, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
1d
Clinical Research Assistant
Pinnacle Clinical Research —Austin, TX
- Full-time
- Spanish
- Vital signs
- Computer literacy
- Health insurance
Quick Apply
Round Rock -Clinical Research Coordinator I
Austin Retina Associates —Round Rock, TX
- Overtime
- Private practice
- Spanish
- Mid-level
Quick Apply
Research Coordinator
IQVIA —Round Rock, TX
- $43,400 - $108,200 a year
- Full-time
- Nursing
- RN License
- 5 years
Clinical Research Coordinator
Planned Parenthood of Greater Texas —Austin, TX
- Weekends as needed
- Spanish
- Microsoft Excel
- Microsoft Outlook
Clinical Research Coordinator
University of Texas at Austin —Austin, TX
- From $55,000 a year
- Urgently hiring
- Mid-level
- Office
- Master's degree
- Retirement plan
Clinical Research Coordinator - Project Hire
Senseye —Austin, TX
- $40,000 - $65,000 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Commuter assistance
Quick Apply
5d
Clinical Research Associate, IQVIA Biotech
IQVIA —Austin, TX
- $71,900 - $169,300 a year
- Full-time
- Bachelor's degree
- Travel
- Experience equivalent to degree accepted
Austin-Clinical Research Coordinator I
Austin Retina Associates —Austin, TX
- Overtime
- Spanish
- 1 year
- Medical terminology
Quick Apply
Clinical Research Coordinator
Tekton Research Inc —Austin, TX
- Full-time
- Mid-level
- High school diploma or GED
- In-person
Quick Apply
2d
Clinical Research Assistant (Round Rock)
Austin Retina Associates —Round Rock, TX
- $18 - $24 an hour
- Overtime
- Bilingual
- Communication skills
- Entry level
- Health savings account
- Disability insurance
Quick Apply
Clinical Study Coordinator
DiaSorin —Austin, TX
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Health insurance
3d
Clinical Research Associate I
University of Texas at Austin —Austin, TX
- From $40,000 a year
- Overtime
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Retirement plan
Austin-Clinical Research Assistant I
Austin Retina Associates —Austin, TX
- Overtime
- Spanish
- High school diploma or GED
- Communication skills
Quick Apply
Clinical Research Assistant
DiaSorin —Austin, TX
- Full-time
- Background check
- Bachelor of Science
- Pass drug screening
2d
Clinical Operations Coordinator
DiaSorin —Austin, TX
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Health insurance
3d
Clinical Care Coordinator
St Davids Care Partners —Austin, TX
- Full-time
- 5 years
- Senior level
- Communication skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Research Project Manager - Project Hire
Senseye —Austin, TX
- $123,000 - $149,000 a year
- Full-time
- 5 years
- English
- Office
- Commuter assistance
Quick Apply
5d

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Clinical Research Associate I

Dell Medical School -
Austin, TX

Quick Apply

Job Details

Full-time
From $40,000 a year

Qualifications

Data quality checks
Nursing
Specimen collection
Microsoft Excel
Clinical study protocols and reports
Quality records maintenance
Microsoft Outlook
Research manuscripts
Scientific publications
Project documentation
CCRA
Operations coordination planning
Master's degree in nursing
Filing
Research project design
Master's degree
Meeting scheduling
Data integrity and documentation
ICH guidelines
Research report preparation
Bachelor's degree
Task prioritization
Health information data integrity
Team training
Industry trends
Data quality monitoring
Project management experience in healthcare
Informed consent procedures implementation
Implementing research protocols
Patient recruitment

Full Job Description

General Notes

This is a grant funded position with an end date of 12/31/2026, renewable based upon availability of funding, work performance, and progress toward research goals. The Clinical Research Associate I will manage and oversee day to day coordination and operations of assigned clinical research projects within the Psychiatry and Behavioral Sciences department. This role involves a significant focus on recruitment, enrollment and research activities for clinical research.

Purpose

The Clinical Research Associate I (CRA I) is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols. Key responsibilities include site management, data collection, and ensuring the integrity of clinical data.

Responsibilities

Site Management

Conducts site initiation, monitoring, and close-out visits.
Ensures compliance with study protocols and regulatory requirements.
Manages site performance and resolves issues.
Supports participant coordination and visit management, including scheduling, visit reminders, and reimbursement processes under PI or senior staff oversight.
Coordinates with clinical staff for specimen collection and protocol-required procedures.

Data Collection and Management

Collects and verifies data from clinical sites.
Ensures accurate and timely data entry into electronic data capture systems.
Reviews and resolves data queries.
Assists with quality control and maintains study binders and source documentation in accordance with GCP and FDA regulations.

Regulatory Compliance

Ensures adherence to Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
Facilitate institutional review board (IRB) applications, submissions, and updates across multiple sites.
Prepares and maintains regulatory documents.
Coordinates with ethics committees to safeguard participant rights.
Supports regulatory start-up activities and assists with IRB amendments under supervision.

Participant Recruitment and Retention

Evaluates medical records and performs screenings to identify eligible study participants.
Assists in screening and enrolling study participants.
Maintains communication with participants to ensure retention.
Addresses participant concerns and queries.
Supports recruitment outreach and preliminary screenings under guidance of senior staff

Reporting and Documentation

Prepares study reports and documentation.
Maintains accurate records of study activities.
Assists in the preparation of manuscripts and publications.

Marginal or Periodic Functions

Conducts literature reviews to support study design and protocol development.
Assists in the training of new site staff and research team members.
Participates in internal and external audits.
Supports the development of study protocols and case report forms.
Attends conferences and workshops to stay updated on industry trends.
Performs other tasks as assigned to support research team and project goals
Adheres to internal controls and reporting structure.
Performs related duties as required.

Knowledge/Skills/Abilities

Double-checks work for errors, maintains organized records, and follows detailed procedures.
Writes clear and concise reports, actively listens to others, and presents information effectively.
Analyzes information, develops solutions, and implements corrective actions.
Shares information, supports team decisions, and contributes to team success.
Prioritizes tasks, sets realistic deadlines, and uses time efficiently.
Basic proficiency in Microsoft Office Suite (Word, Excel, Outlook). Familiarity with data entry platforms such as REDCap or ability and willingness to learn.
Demonstrated ability to collaborate effectively with participants, clinical staff, and research teams.
Detail-oriented with strong time management; able to follow protocols and maintain regulatory compliance.

Required Qualifications

Requires a Bachelor's Degree in life sciences, nursing, or a related field.
1 year of relevant clinical research experience.
Relevant education and experience may be substituted as appropriate

Preferred Qualifications

Master's Degree in life sciences, nursing, or a related field. with at least 2 year(s) of experience in clinical research experience.
Experience in research or healthcare environment (e.g., internships, volunteer roles, or academic projects).
Good Clinical Practice (GCP) Certification: Demonstrates understanding of GCP guidelines.

Licenses, Registrations or Certifications

None

Preferred:

Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).
CITI Human Subjects Research Training.
GCP (Good Clinical Practice) certification.

Salary Range

$40,000 + depending on qualifications

Working Conditions

May work around chemical fumes
May work around standard office conditions
May work around biohazards
May work around chemicals
Repetitive use of a keyboard at a workstation
Use of manual dexterity
Climbing of stairs
Climbing of ladders
Lifting and moving
Occasional weekend, overtime and evening work to meet deadlines

Required Materials

Resume/CV
3 work references with their contact information; at least one reference should be from a supervisor
Letter of interest

Important for applicants who are NOT current university employees or contingent workers: You will be prompted to submit your resume the first time you apply, then you will be provided an option to upload a new Resume for subsequent applications. Any additional Required Materials (letter of interest, references, etc.) will be uploaded in the Application Questions section; you will be able to multi-select additional files. Before submitting your online job application, ensure that ALL Required Materials have been uploaded. Once your job application has been submitted, you cannot make changes.

Important for Current university employees and contingent workers: As a current university employee or contingent worker, you MUST apply within Workday by searching for Find UT Jobs. If you are a current University employee, log-in to Workday, navigate to your Worker Profile, click the Career link in the left hand navigation menu and then update the sections in your Professional Profile before you apply. This information will be pulled in to your application. The application is one page and you will be prompted to upload your resume. In addition, you must respond to the application questions presented to upload any additional Required Materials (letter of interest, references, etc.) that were noted above.

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Refine Your Search

clinical research coordinator jobs in round rock tx

Clinical Research Associate I

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Assistant

Round Rock -Clinical Research Coordinator I

Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator - Project Hire

Clinical Research Associate, IQVIA Biotech

Austin-Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Assistant (Round Rock)

Clinical Study Coordinator

Clinical Research Associate I

Austin-Clinical Research Assistant I

Clinical Research Assistant

Clinical Operations Coordinator

Clinical Care Coordinator

Clinical Research Project Manager - Project Hire

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