Top 22 Research coordinator Jobs in Round Rock, Tx

Research Coordinator
IQVIA —Round Rock, TX
- $43,400 - $108,200 a year
- Full-time
- Nursing
- RN License
- 5 years
Clinical Research Coordinator I
U.S. Dermatology Partners —Cedar Park, TX
- $55,000 - $65,000 a year
- Full-time
- Vital signs
- Microsoft Outlook
- Computer literacy
- Paid holidays
- Health insurance
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 - Project Hire
Senseye —Austin, TX
- $40,000 - $65,000 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Commuter assistance
Quick Apply
1d
Senior Research Program Coordinator
University of Texas at Austin —Austin, TX
- From $63,000 a year
- Urgently hiring
- Microsoft Outlook
- Office
- 3 years
- Retirement plan
21h
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
Round Rock -Clinical Research Coordinator I
Austin Retina Associates —Round Rock, TX
- Overtime
- Private practice
- Spanish
- Mid-level
Quick Apply
Project Coordinator
University of Texas at Austin —Austin, TX
- $70,000 a year
- Weekends as needed
- Nursing
- English
- Mid-level
- Retirement plan
1d
Clinical Research Coordinator
Planned Parenthood of Greater Texas —Austin, TX
- Weekends as needed
- Spanish
- Microsoft Excel
- Microsoft Outlook
Preclinical Study Coordinator
Neuralink —Austin, TX
- $31 - $53 an hour
- Full-time
- Master's degree
- Bachelor's degree
- 1 year
- Commuter assistance
- Paid holidays
Clinical Research Coordinator / Recruiter
Eurofins USA Consumer Product Testing —Austin, TX
- Part-time
- Customer service
- Computer literacy
- HIPAA
Quick Apply
Ending the HIV Epidemic Coordinator
Dept of State Health Services —Austin, TX
- $5,425.33 - $7,155.75 a month
- Online Application
- Office
- Travel
- Military encouraged
Quick Apply
Site Regulatory/ Data Coordinator
Sarah Cannon Research Institute —Austin, TX
- Full-time
- Microsoft Outlook
- Writing skills
- Mid-level
Senior Research Program Coordinator - Texas Center for Disability Studies
University of Texas at Austin —Austin, TX
- $60,000 - $70,000 a year
- Weekends as needed
- Microsoft Word
- Spanish
- Microsoft Excel
- Retirement plan
6d
Austin-Clinical Research Coordinator I
Austin Retina Associates —Austin, TX
- Overtime
- Spanish
- 1 year
- Medical terminology
Quick Apply
Site Regulatory/ Data Coordinator
McKesson —Austin, TX
- Microsoft Outlook
- Writing skills
- Mid-level
Grant Management Coordinator, College of Pharmacy, Pharmacy Addictions Research and Medicine Program
University of Texas at Austin —Austin, TX
- From $73,992 a year
- Full-time
- Mid-level
- Office
- Administrative experience
- Paid holidays
- Loan forgiveness
Public Policy Coordinator, Trauma and Mental Health
TEXAS COUNCIL ON FAMILY VIOLENCE —Austin, TX
- Weekends as needed
- Hybrid work
- Spanish
- English
- Mid-level
Quick Apply

More jobs to discover

Find similar jobs that you might be interested in.

Clinical Research Coordinator I
U.S. Dermatology Partners —Cedar Park, TX
Knowledge of state and federal regulations such as ICH GCP, IATA; general understanding of HIPAA guidelines. Assist clinical research manager in delegated tasks…
$55,000 - $65,000 a year
Quick Apply
Round Rock -Clinical Research Coordinator I
Austin Retina Associates —Round Rock, TX
Communicate and coordinate with study sponsor, monitors, and CRO's including data entry queries, audits and monitoring visits. Experience with Real Time CTMS.
Quick Apply

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

Show more jobs in cities nearby

I want to receive the latest job alert for research coordinator in round rock, tx

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

research coordinator jobs near round rock, tx

Research Coordinator jobs in Round Rock, TX

Site Coordinator jobs in Austin, TX

Grants Manager jobs in Austin, TX

Clinical Research Coordinator jobs in Austin, TX

Research Program Coordinator jobs in Austin, TX

Public Health Coordinator jobs in Austin, TX

Clinical Research Coordinator jobs in Round Rock, TX

Clinical Research Coordinator jobs in Pflugerville, TX

Project Coordinator jobs in Austin, TX

Research Coordinator jobs in Athens, GA

Logistics Coordinator jobs in Boston, MA

Research Coordinator jobs in Denton, TX

Research Coordinator jobs in Tampa, FL

Authorization Coordinator jobs in Los Angeles, CA

Research Coordinator jobs in Davis, CA

Wellness Coordinator jobs in Pennsylvania

Site Coordinator jobs in Tunnel Hill, GA

Site Coordinator jobs in Stanwood, WA

Site Coordinator jobs in Chicago, IL

Site Safety Manager jobs in New York, NY

Research Coordinator

IQVIA -
Round Rock, TX

Apply Now

Job Details

Full-time
$43,400 - $108,200 a year

Qualifications

Bachelor's degree
Oncology

Full Job Description

The Research Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. Research Coordinators assist with screening patients, schedule, and oversee all on-study requirements. Research Coordinators attend study teleconferences with sponsors and clinical research organizations to assure continuity of information.

Essential Duties and Responsibilities

Essential and other important responsibilities and duties may include but are not limited to the following:

Protocol Compliance

Identifies primary and secondary study objectives and outcome measures
Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research
Complies with NEXT Oncology SOPs
Participates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timelines of protocol-related procedures
Collaborates with the Principal Investigator, pharmacy, and other appropriate personnel to ensure proper use of and accountability for study drugs
Provides protocol specific education to clinical staff
Facilitates and participates in the preparation for an conduct of meetings/teleconferences with sponsors, monitors, and auditors
Provides timely, accurate, and complete reporting of serious adverse events, unanticipated problems, deviations, violations, and noncompliance to the IRB and sponsor
Contributes to the development of corrective and preventive action plans for unanticipated problems, deviations, violations, and issues of noncompliance

Informed Consent

Identifies and intervenes to address barriers to effective informed consent discussions
and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception)
Describes and abides by institutional policy and processes for informed consent
Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient
Collaborates with the physician investigator to ensure initial and ongoing consent process is performed and documented
Assesses ongoing consent through discussions with patients and reinforcement of education
Assesses patient’s understanding of the information provided during the informed consent process
Ensures timely re-consenting as needed by the physician investigator
Demonstrates understanding of tiered consent process when optional correlative studies
(e.g., biospecimen, quality of life, patient-reported outcomes collections) are involved
Confirms informed consent is obtained prior to performing any study specific tasks

Management of Clinical Trial Patients

Collaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol
Educates the patient and family regarding protocol participation
Provides patient education regarding required study procedures
If the Research Coordinator is a Registered Nurse, educates the patient and family regarding clinical condition, and/or disease process. If the Research Coordinator is not a RN, he/she will schedule educational time with a RN
If the Research Coordinator is a Registered Nurse, identifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety. If the Research Coordinator is not an RN, he/she will schedule educational time with a RN
Coordinates, schedules, and ensures timely completion of protocol-required events and other requirements (e.g., pharmacokinetics or –dynamics, scans, study visits, QOL,)
Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary
Evaluates patient’s adherence to and documentation of self-administered protocol agents and the return of such agents
Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers
Evaluates patient’s adherence to and documentation of self-administered protocol agents and return of such agents
Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers
Ensures appropriate communication between research and clinical staff related to patient-specific care needs
Ensures evidence-based symptom management as permitted by the protocol

Documentation and Document Management

Documents all patient encounters in the legal medical record per licensure and institutional requirements
Obtains documents from outside providers or laboratories that are needed as part of the research data
Educates other research team members and clinical staff regarding appropriate and accurate source documentation for patients of in clinical trials
Assesses documentation or discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents
Maintains the privacy and confidentiality of patients' source documents
Maintains specified study documents in the Research Coordinator files
Participates in the development of approved source documents, templates, or forms

Data Management and Information Technology

Adheres to the data management plan per NEXT SOPs and sponsor data management plan
Assists in troubleshooting data entry issues
Ensures that relevant data from source documents are abstracted and entered into CRFs in a timely and accurate manner
Ensure that data recorded on the CRFs can be verified within the source documents
Participates in quality control activities to ensure data integrity, including timely responses to database or sponsor queries
Enters data into electronic data capture for SAEs as appropriate

Required Education and Experience

The Research Coordinator must be knowledgeable of standard research and oncology care practices
Typically requires 5 or more years of experience
Current Texas or Virginia Registered Nursing License for RNs
Bachelor's degree required for non-RNs
Oncology clinical trial experience preferred
Research Coordination experience preferred

Why Join Us?

At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $43,400.00 - $108,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Apply Now

Refine Your Search

research coordinator jobs in round rock, tx

Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator - Project Hire

Senior Research Program Coordinator

Clinical Research Coordinator

Round Rock -Clinical Research Coordinator I

Project Coordinator

Clinical Research Coordinator

Preclinical Study Coordinator

Clinical Research Coordinator / Recruiter

Ending the HIV Epidemic Coordinator

Site Regulatory/ Data Coordinator

Senior Research Program Coordinator - Texas Center for Disability Studies

Austin-Clinical Research Coordinator I

Site Regulatory/ Data Coordinator

Grant Management Coordinator, College of Pharmacy, Pharmacy Addictions Research and Medicine Program

Public Policy Coordinator, Trauma and Mental Health

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for research coordinator in round rock, tx

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected