Top 115 Clinical research Jobs in Austin, Tx

Clinical Research Assistant
Pinnacle Clinical Research —Austin, TX
- Full-time
- Spanish
- Vital signs
- Computer literacy
- Health insurance
Quick Apply
14d
Clinical Research Assistant
DiaSorin —Austin, TX
- Full-time
- Background check
- Bachelor of Science
- Pass drug screening
4h
Assoc Clinical Research Mgr
Thermo Fisher Scientific —Austin, TX
- Full-time
- Hospital
- Computer literacy
- Clinic
6d
Clinical Research Coordinator
Planned Parenthood of Greater Texas —Austin, TX
- Weekends as needed
- Spanish
- Microsoft Excel
- Microsoft Outlook
Research Associate I
University of Texas at Austin —Austin, TX
- From $40,000 a year
- Urgently hiring
- Psychiatry
- Office
- Master's degree
- Retirement plan
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 Operations Coordinator
DiaSorin —Austin, TX
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Health insurance
1d
Clinical Study Coordinator
DiaSorin —Austin, TX
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Health insurance
1d
Research Coordinator
IQVIA —Austin, TX
- $43,400 - $108,200 a year
- Full-time
- Nursing
- RN License
- 5 years
Associate Clinical Research Manager
Thermo Fisher Scientific —Austin, TX
- Full-time
- Computer literacy
- Mid-level
- Clinic
6d
CRA 1, IQVIA Biotech
IQVIA —Austin, TX
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
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
Dermatologists of Central States —Pflugerville, TX
- Nursing
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Operations Analyst II
University of Texas at Austin —Austin, TX
- From $61,039 a year
- Full-time
- Customer service
- Mid-level
- Office
- Retirement plan
1d
Clinical Research Manager
Thermo Fisher Scientific —Austin, TX
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
6d
Social Science/Humanities Research Associate I
University of Texas at Austin —Austin, TX
- $40,000 a year
- Urgently hiring
- Spanish
- Adults
- English
- Retirement plan
14d
Clinical Research Coordinator - Project Hire
Senseye —Austin, TX
- $40,000 - $65,000 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Commuter assistance
Quick Apply
3d
Clinical Data Scientist
DiaSorin —Austin, TX
- Full-time
- Background check
- Writing skills
- Pass drug screening
1d
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

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Clinical Research Assistant

Pinnacle Clinical Research -
Austin, TX

Quick Apply

Job Details

Full-time
14 days ago

Benefits

Health insurance

Qualifications

Spanish
Medical software
Enterprise software
Spreadsheets
Word embeddings
English
Productivity software

Full Job Description

Summary: Assists the Clinical Research Coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites. Exercises judgment within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the study Investigator and supervisor. Always maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties.

Duties and Responsibilities:

Assists with the creation and completion of study related documents and new study preparation.
Assists with the completion of regulatory submissions and maintains regulatory files as directed.
Acts as a secondary liaison with sponsors.
Assists with the preparation for study monitor visits as directed.
Completes case report forms as directed.
Creates reports as requested.
Completes study directed assessments with patients to include, but not limited to adverse events, test article (TA) handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment.
Assists with subject screening and recruitment as directed.
Updates Clinical Trial Management Software (CTMS) as directed.
Coordinates multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume.
Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.

Duties, responsibilities, and activities may change, or new ones assigned at any time.

Education Experience:

High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.

Certificates and Licenses:

Clinical research certification preferred

Knowledge, Skills, and Other Abilities:

Ability to demonstrate competence in oral and written communication
Bilingual (English/Spanish) required
Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Medical knowledge, including medical terminology
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.

Work Environment and Physical demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work is performed in an office/laboratory and/or a clinical environment.
Exposure to biological fluids and/or bloodborne pathogens.
Personal protective equipment required such as protective eyewear, garments, and gloves.
Occasional travel may be required domestic and/or international.
Ability to work in an upright and/or stationary position for 6-10 hours per day.
Frequent mobility required.
Occasional squatting, kneeling, or bending.
Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.

Quick Apply

Refine Your Search

clinical research jobs in austin, tx

Clinical Research Assistant

Clinical Research Assistant

Assoc Clinical Research Mgr

Clinical Research Coordinator

Research Associate I

Clinical Research Associate I

Austin-Clinical Research Assistant I

Clinical Operations Coordinator

Clinical Study Coordinator

Research Coordinator

Associate Clinical Research Manager

CRA 1, IQVIA Biotech

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Operations Analyst II

Clinical Research Manager

Social Science/Humanities Research Associate I

Clinical Research Coordinator - Project Hire

Clinical Data Scientist

Clinical Research Assistant (Round Rock)

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