Clinical Research Coordinator
Clinical Research Coordinator
Posted on :
05-07-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
05-07-2025
Job Description
Austin Institute for Clinical Research (AICR) is seeking aClinical Research Coordinator(CRC) for our Pflugerville office who is an expert with managing clinical pharmaceutical and device protocols. TheClinical Research Coordinatormust be organized and willing to work a problem to its successful completion.
Performance Objectives:
- Represents AICR in a professional and courteous manner (verbal written and in appearance) when interacting with AICR staff sponsors IRBs and subjects.
- Must be moral and ethical in decision making and during interaction with patients sponsor and IRB representatives physicians and other staff.
- Maintains ongoing communication with Director of Research Associate Director of Research Principal Investigator/Sub-Investigator other study personnel and sponsor/CRO per AICR SOPs and as deemed necessary.
- Possesses a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
- Maintains confidentiality of patient and/or protocol issues as appropriate and as bound by Confidentiality Agreements with AICR between AICR and sponsors and between AICR and other entities.
- Is creative and diligent in the recruitment of qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsors timeline while following all policies and regulations governing medical ethics IRB requirements federal regulations/ICH guidelines GCPs and AICRs SOPs.
- Has training certificate in and competently perform pediatric/adult phlebotomy.
- Obtains blood and urine samples and then processes and ships specimens as required.
- Able to accomplish protocol specified patient visits and procedures.
- Clearly and concisely documents patient assessments observations test results and other study related information per federal regulations/ICH guidelines GCPs AICRSOPs sponsor/CRO and IRB requirements.
- Maintains accurate and complete written source documentation of patient visits and protocol related activities.
- Accurately completes CRFs/eCRFs and/or worksheets generated by the sponsor/CRO within 1 to 3 business days of the subjects visit.
- Maintains subject screening logs and protocol deviation logs.
- Responds to monitor notes and/or emails in a timely manner.
- Accounts for clinical trial materials (i.e. CRFs study drug lab supplies and/or other required items) and ensures availability of appropriate amounts for the conduct of the study.
- Attends required training courses/conferences in order to stay abreast of current and changing federal regulations and AICR policies.
- Attends Investigator Meetings as directed.
- Performs all duties in a safe and prudent manner.
- Promptly reports adverse events to Associate Director of Research Principal.
- Other duties as assigned.
Position Requirements
- Associate or Bachelors Degree preferred.
- At least two (2) years of previous research and/or clinical experience is required.
- Excellent organizational and communication skills both verbal and written.
- Integrity and confidentiality.
At AICR employees are our most valuable resources and an integral part of our success.
Come see what its like to have an amazing employee experience with one of the best teams in the clinical research world.
PERKS OF JOINING OUR TEAM!
- We valueIntegrity Teamwork Compassion Innovation&Excellence
- Competitive Salary
- Great Healthcare Plan for you and all dependents (we help you out with the cost!)
- Voluntary Dental Vision STD Accident LTD and Life
- Retirement contribution with Company match
- Company provided life insurance
- Paid Time off (PTO)
- Parental leave
- Paid holidays
- Company sponsored events
- Employee rewards and recognition programs
- An environment in which you can balance great work with a great life
AICR is an Equal Opportunity Employer
Required Experience:
IC
Employment Type
Full Time
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