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Clinical Research Associate I/II/III

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Closing Date:

06/03/2025


Type of Position:


Job Type:

Regular


Work Shift:

Sponsorship Available:

No


Institution Name:

University of Arkansas for Medical Sciences


The University of Arkansas for Medical Sciences (UAMS) has a unique combination of education, research, and clinical programs that encourages and supports teamwork and diversity. We champion being a collaborative health care organization, focused on improving patient care and the lives of Arkansans.
 

UAMS offers amazing benefits and perks (available for benefits eligible positions only):

  • Health: Medical, Dental and Vision plans available for qualifying staff and family
  • Holiday, Vacation and Sick Leave
  • Education discount for staff and dependents (undergraduate only)
  • Retirement: Up to 10% matched contribution from UAMS
  • Basic Life Insurance up to $50,000
  • Career Training and Educational Opportunities
  • Merchant Discounts
  • Concierge prescription delivery on the main campus when using UAMS pharmacy

Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening.  To apply for the position, please click the Apply link/button.

The University of Arkansas is an equal opportunity institution. The University does not discriminate in its education programs or activities (including in admission and employment) on the basis of any category or status protected by law, including age, race, color, national origin, disability, religion, protected veteran status, military service, genetic information, sex, sexual preference, or pregnancy. Federal law prohibits the University from discriminating on these bases. Questions or concerns about the application of Title IX, which prohibits discrimination on the basis of sex, may be sent to the University's Title IX Coordinator and to the U.S. Department of Education Office for Civil Rights.

Persons must have proof of legal authority to work in the United States on the first day of employment.

All application information is subject to public disclosure under the Arkansas Freedom of Information Act.
 

For general application assistance or if you have questions about a job posting, please contact Human Resources at askrecruitment@uams.edu.


Department:

COM | PSY Health & Legal Sys Lab


Department's Website:


Summary of Job Duties:

The Clinical Research Associate I/II/III will coordinate research projects and/or federally-funded grants under the direction of the Principal Investigator (PI), Dr. Melissa Zielinski, within UAMS’ Health and the Legal System Research, Practice, and Policy Lab. The team’s work often focuses on the intersections between traumatic stress, addiction, and incarceration, with a particular focus on the implementation of evidence-based interventions for posttraumatic stress in legal settings and on the health of justice-involved women. The Clinical Research Associate I/II/III will need to be comfortable managing multiple projects and have advanced organizational skills for meeting deadlines, project deliverables, and enrollment goals and coordinating meetings and activities across project partners. This position requires the willingness to undertake regular local, in-state travel (rarely, but occasionally, overnight) and requires the willingness to work variable hours to meet the needs of assigned projects and participants (e.g., nights and weekends).


Qualifications:

Level I

  • Bachelor's degree plus three (3) years of research-related experience required.

  • Obtain Certified Research Specialist (CRS) certification within 2 years of hire.

Level II

  • Bachelor's degree plus three (3) years of research-related experience with demonstrated proficiency in a functional area required.

  • Obtain CRS certification within 2 years of hire.

Level III

  • Bachelor's degree plus five (5) years of research-related experience with demonstrated proficiency in a functional area required.

  • Certified Clinical Research Professional (CCPR), Certified Clinical Research Associate (CCRA), or equivalent professional certification.

Knowledge, Skills & Abilities:

  • Must have excellent computer skills.

  • Ability to use the Microsoft Office suite at a high level of proficiency is essential. 

  • Excellent written and verbal communication skills.

  • Ability to work collaboratively and sensitively with incarcerated individuals and with community partners.

  • Must be able to drive for in-state travel.

  • Proficiency with online survey software (REDCap, Qualtrics) preferred.

  • Knowledge of human subjects’ behavioral research preferred.

  • Experience conducting research with vulnerable populations in the area of traumatic stress ( i.e., incarcerated persons, people with PTSD) preferred.


Additional Information:

Responsibilities:

  • Manages research team schedules.

  • Maintains calendar and provides scheduling assistance for the Principal Investigator and project teams.

  • Schedules grant-related meetings (e.g., speaker series, research meetings, study/project participant assessment sessions).

  • Works with internal and external partners to facilitate project activities, including working with department administration to acquire needed equipment/programs.

  • Assists with participant assessment, scheduling, and retention efforts and with informing the broader research team of study activities to promote coordination across projects.

  • Sets meeting agendas, takes notes, and distributes after-meeting action items.

  • Engages with organizations and agencies to accomplish research objectives.

  • Develops tools to track research team metrics and reports. Updates tracking tools regularly.

  • Bears primary responsibility for ensuring that laboratory space is clean and organized. Monitors and manages laboratory supplies.

  • May oversee other staff and/or student trainees in executing project activities, including data collection.

  • Performs initial contact with prospective research subjects.

  • Monitors the information for eligibility for the specific protocol as well as accuracy and completeness prior to examination by the investigators and/or sponsoring agency. 

  • Collects, codes, and enters study information into a database.

  • Assists in data compilation. 

  • Maintains records and study information, and prepares reports and summaries as needed.

  • Ensures that completed questionnaires are complete, legible, and accurate in accordance with research protocols. 

  • Makes follow-up contact with participants to obtain missing or questionable data.

  • Maintains complete & accurate records and files pertaining to one or more research studies. 

  • Maintains detailed records of research subject visits and procedures.

  • Transcribes qualitative data and prepares for upload to qualitative analysis software.

  • Conducts qualitative coding.

  • Makes descriptive reports of research study progress and outcomes.

  • Builds instructions for scoring research assessments.

  • May conduct more advanced analyses under the direction of the PI.

  • Assists in the preparation and submission of grant proposals, grant reports, manuscripts, and lay reports.

  • Reviews literature for related research developments & compiles findings

  • Performs other duties as assigned.


Salary Information:

Commensurate with education and experience


Required Documents to Apply:

Resume


Optional Documents:


Special Instructions to Applicants:


Recruitment Contact Information:

Please contact askrecruitment@uams.edu for any recruiting related questions.


All application materials must be uploaded to the University of Arkansas System Career Site https://uasys.wd5.myworkdayjobs.com/UASYS  

Please do not send to listed recruitment contact.


Pre-employment Screening Requirements:


This position is subject to pre-employment screening (criminal background, drug testing, and/or education verification). A criminal conviction or arrest pending adjudication alone shall not disqualify an applicant except as provided by law. Any criminal history will be evaluated in relationship to job responsibilities and business necessity.  The information obtained in these reports will be used in a confidential, non-discriminatory manner consistent with state and federal law. 


Constant Physical Activity:


Frequent Physical Activity:


Occasional Physical Activity:


Benefits Eligible:

Yes

Average salary estimate

$65000 / YEARLY (est.)
min
max
$50000K
$80000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Clinical Research Associate I/II/III, UASYS

Are you excited by the idea of making a real difference in the world of health and legal systems? The University of Arkansas for Medical Sciences (UAMS) is looking for a Clinical Research Associate I/II/III to join our dynamic Health and the Legal System Research, Practice, and Policy Lab. In this role, you'll collaborate with our Principal Investigator, Dr. Melissa Zielinski, to coordinate vital research projects and federally-funded grants that focus on the intersections of traumatic stress, addiction, and incarceration. As a Clinical Research Associate, you'll not only manage multiple projects but also work with a passionate team dedicated to implementing evidence-based interventions for justice-involved women. Your advanced organizational skills will come into play as you meet deadlines and work diligently towards project deliverables, while you collaborate with various project partners. The position requires a willingness to travel locally and occasionally work variable hours to meet project needs. With a Bachelor’s degree and relevant research experience under your belt, this could be a fantastic opportunity for you to bring your expertise to our committed team. By joining UAMS, you will not only contribute to essential research but also enjoy great benefits, including health coverage, vacation time, and competitive retirement contributions. Ready to take the next step? Discover how your skills and passion can contribute to our vital work!

Frequently Asked Questions (FAQs) for Clinical Research Associate I/II/III Role at UASYS
What are the responsibilities of a Clinical Research Associate I/II/III at the University of Arkansas for Medical Sciences?

As a Clinical Research Associate I/II/III at the University of Arkansas for Medical Sciences, your responsibilities will include managing research team schedules, coordinating grant-related meetings, assisting with participant assessments, and maintaining accurate research records. You will also engage with community organizations to meet research objectives and monitor laboratory supplies to ensure a well-organized work environment.

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What qualifications do I need to become a Clinical Research Associate at UAMS?

To qualify for the Clinical Research Associate role at the University of Arkansas for Medical Sciences, you need a Bachelor’s degree along with relevant research experience: at least three years for Level I and II, and a minimum of five years for Level III. Additionally, you are expected to gain Certified Research Specialist (CRS) certification within two years of hire for Levels I and II, while Level III requires certification as a Clinical Research Professional (CCRP) or a Clinical Research Associate (CCRA).

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What skills are essential for a Clinical Research Associate at UAMS?

Essential skills for a Clinical Research Associate at the University of Arkansas for Medical Sciences include excellent computer skills, proficiency with the Microsoft Office suite, outstanding written and verbal communication abilities, and capabilities to work sensitively with incarcerated individuals and community partners. Familiarity with online survey software such as REDCap and Qualtrics is also preferred.

Join Rise to see the full answer
Is prior experience with vulnerable populations necessary for the Clinical Research Associate role at UAMS?

While prior experience conducting research with vulnerable populations, particularly in areas of traumatic stress, is preferred for the Clinical Research Associate position at the University of Arkansas for Medical Sciences, it is not strictly mandatory. However, candidates with such experience may have a beneficial edge in understanding the complexities of research in sensitive environments.

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What kind of projects will a Clinical Research Associate be working on at UAMS?

A Clinical Research Associate at the University of Arkansas for Medical Sciences will work on projects that focus on the intersections of traumatic stress, addiction, and incarceration. This may include implementing evidence-based interventions for posttraumatic stress in legal settings and participating in research surrounding the health of justice-involved women. You will directly engage with various research teams and community partners to further these objectives.

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Common Interview Questions for Clinical Research Associate I/II/III
Can you describe your experience with managing research projects as a Clinical Research Associate?

When answering this question, focus on specific projects you’ve managed, highlighting your organizational skills, attention to detail, and ability to meet deadlines. Provide examples of how you handled challenges and ensured project deliverables were met on time.

Join Rise to see the full answer
How do you ensure compliance with research protocols when working with vulnerable populations?

In your response, emphasize your understanding of ethical considerations and guidelines when working with vulnerable populations. Discuss any relevant training you've had and how you approach participant recruitment, retention, and data management while ensuring ethical compliance.

Join Rise to see the full answer
What methods do you use to maintain effective communication with research teams?

To answer this, highlight your experience using various communication tools and methods. Discuss your strategies for keeping everyone informed about project statuses, setting meeting agendas, and distributing action items post-meetings. Show that you value transparency and collaboration.

Join Rise to see the full answer
Can you give an example of a time when you had to work under pressure to meet project deadlines?

When responding to this question, share a specific situation where you faced tight deadlines. Explain the steps you took to prioritize tasks, communicate with team members, and ultimately achieve your goals, showcasing your ability to perform well under stress.

Join Rise to see the full answer
How do you approach data collection and entry in research studies?

Detail the systems and strategies you use to ensure data accuracy and integrity. Describe how you manage data entry processes and the importance of maintaining detailed records, as well as any software you are proficient with, like REDCap or Qualtrics.

Join Rise to see the full answer
What experience do you have with grant proposals or reports?

Discuss any involvement you’ve had with preparing grant proposals or reports at previous roles. Highlight your ability to follow guidelines, collaborate with co-authors, and contribute substantial content that helps secure funding or effectively communicates project outcomes.

Join Rise to see the full answer
How would you handle conflicts within a research team?

Your answer should reflect your conflict resolution skills. Provide an example of a past conflict, the resolution process you followed, and the importance of maintaining a positive working environment that encourages collaboration and open dialogue.

Join Rise to see the full answer
In what ways do you stay updated on developments in clinical research?

Share your strategies for professional development, such as attending workshops, webinars, or conferences related to clinical research. Mention any professional organizations you're involved with, and how you actively seek out new information in your field to stay current.

Join Rise to see the full answer
Describe a situation where you had to engage with community partners to achieve research objectives.

Provide an example of a project where collaboration with community partners was essential. Discuss how you established relationships, communicated needs, and managed expectations to align project goals with partner capabilities.

Join Rise to see the full answer
What motivates you to work in the field of clinical research?

In your response, be genuine about your passion for improving health outcomes and contributing to scientific knowledge. Illustrate how your personal values align with the mission of the University of Arkansas for Medical Sciences and why you are eager to engage in this meaningful work.

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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
April 6, 2025

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