Top 50 Clinical research associate Jobs in Austin Tx

Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central US
Thermo Fisher Scientific —Texas
- Full-time
- Nursing
- RN License
- Writing skills
1d
Clinical Research Associate
DiaSorin —Austin, TX
- Full-time
- Background check
- Bachelor of Science
- Pass drug screening
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
Clinical Laboratory Project Assistant
Thermo Fisher Scientific —Austin, TX
- Full-time
- Office
- Quality control
- Entry level
3d
Clinical Scientist
Neuralink —Austin, TX
- $108,000 - $200,000 a year
- Full-time
- 5 years
- Mid-level
- Analysis skills
- Commuter assistance
- Paid holidays
Clinical Research Assistant
Pinnacle Clinical Research —Austin, TX
- Full-time
- Spanish
- Vital signs
- Computer literacy
- Health insurance
Quick Apply
5d
Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Austin, TX
- English
- Mid-level
- Ability to sit for extended periods
- Paid holidays
- Health insurance
Quick Apply
14d
Clinical Research Associate I
University of Texas at Austin —Austin, TX
- From $40,000 a year
- Overtime
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Retirement plan
Clinical Research Associate
XBiotech USA, Inc —Austin, TX
- Full-time
- Nursing
- Mid-level
- 3 years
- Health savings account
- Health insurance
Quick Apply
14d
Research Scientist
Dell Medical School —Austin, TX
- From $80,000 a year
- Overtime
- Office
- Master's degree
- University
Quick Apply
Manager, Clin Ops - FSP
Thermo Fisher Scientific —Austin, TX
- Full-time
- Remote
- English
- Office
- Business development
1d
Clinical Research Associate I
Dell Medical School —Austin, TX
- From $40,000 a year
- Full-time
- Nursing
- Bachelor's degree
- 1 year
Quick Apply
Project Manager (Clinical Trials - Central Laboratory)
Sonic Clinicals Trials USA, Inc —Austin, TX
- Full-time
- Customer service
- Bachelor of Science
- Mid-level
Clinical Research Nurse (RN)
Texas Oncology —Austin, TX
- Full-time
- Nursing
- RN License
- BLS Certification
- Wellness program
- Disability insurance
Clinical Research Coordinator
Planned Parenthood of Greater Texas —Austin, TX
- Weekends as needed
- Spanish
- Microsoft Excel
- Microsoft Outlook
Late Phase Clinical Research Manager
Thermo Fisher Scientific —Austin, TX
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
Research Associate
The Specialty Alliance —Austin, TX
- $17 - $18 an hour
- Part-time
- Vital signs
- HIPAA
- Clinic
Quick Apply
Clinical Research Coordinator
Pinnacle Clinical Research —Austin, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator
University of Texas at Austin —Austin, TX
- From $53,454 a year
- Urgently hiring
- Mid-level
- Office
- 3 years
- Retirement plan
Clinical Research Nurse Practitioner / Physician Assistant (Sub-Investigator) - Austin, TX
The IMA Group —Austin, TX
- Full-time
- Mid-level
- 2 years
- Paid parental leave
- Paid holidays
Quick Apply

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Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central US

Thermo Fisher Scientific -
Texas

Apply Now

Job Details

Full-time
1 day ago

Qualifications

Customer communication
Driver's License

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as an FSP Clinical Research Associate (Level I or II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As an FSP Clinical Research Associate (Level I or II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines for one specific sponsor. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.
Participates in investigator meetings as necessary.

Engages directly with sponsor staff and complimentary workers on a daily basis.
investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related fieldor a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
Valid driver's license where applicable.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexibile and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions

Apply Now

Refine Your Search

clinical research associate jobs in austin tx

Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central US

Clinical Research Associate

Clinical Research Associate, IQVIA Biotech

Clinical Laboratory Project Assistant

Clinical Scientist

Clinical Research Assistant

Clinical Research Coordinator I

Clinical Research Associate I

Clinical Research Associate

Research Scientist

Manager, Clin Ops - FSP

Clinical Research Associate I

Project Manager (Clinical Trials - Central Laboratory)

Clinical Research Nurse (RN)

Clinical Research Coordinator

Late Phase Clinical Research Manager

Research Associate

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Nurse Practitioner / Physician Assistant (Sub-Investigator) - Austin, TX

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