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Clinical Data Coordinator

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Closing Date:

04/30/2025


Type of Position:

Researchers


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:

CI | Coordinator Team C


Department's Website:


Summary of Job Duties:

This role involves supporting oncology clinical trials by managing data collection and entry for pharmaceutical, cooperative group, and investigator-initiated studies. The duties include ensuring data integrity by adhering to ALCOA+C principles (Attributable, Legible, Contemporaneous, Original, Accurate, and Complete), timely data submission, and effective communication with Clinical Research Coordinators (CRC), managers, nurses, and other stakeholders. The position requires organizing complex projects, providing attention to detail, and maintaining knowledge of regulatory standards.

"This position reports to UAMS in Little Rock, AR – applicants must reside in Arkansas"


Qualifications:

Minimum:

  • Bachelor’s Degree plus two (2) years of project management, data collection, data entry, or relatable experience OR Associate's degree plus 4 years' project management, data collection, data entry or relatable experience OR High School Diploma or GED plus 6 years of project management, data collection, data entry, or relatable experience 

  • Obtain CRS certification within 2 years of hire.

Special knowledge, skills, and abilities: 

  • Ability to operate under close supervision, receiving instructions on routine work and general instructions on routine assignments.
  • Skill and ability to communicate with others verbally or in writing to provide or obtain information.
  • Skill and ability to perform moderately varied tasks requiring some interpretation of results within a moderate scope and a review of identifiable factors.
  • Familiarity with medical terminology.
  • Skill and ability to compile, analyze, and summarize data.
  • Knowledge and skill with word processing, spreadsheet, and e-mail computer software (e.g., Microsoft Word, Excel, Outlook).
  • Skill and ability to organize and prioritize tasks.
  • Skill and ability to attend to details.
  • Skill and ability to cope with work activities that may be repetitive in nature.
  • Ability to maintain confidentiality of data and records.

Preferred: 

  • Bachelor’s degree
  • Clinical research experience, Oncology experience, data collection experience.

This position reports to UAMS in Little Rock, AR – applicants must reside in Arkansas


Additional Information:

Responsibilities:

  • Performs data collection and entry to support CCTRA oncology clinical trials, including pharmaceutical-sponsored, cooperative group, and investigator-initiated trials.

  • Ensures data follows the ALCOA+C (Attributable, Legible, Contemporaneous, Original, Accurate, and Complete) principles for good clinical research documentation.

  • Organizes complex projects, provides attention to detail, and communicates effectively with team members and stakeholders.

  • Works closely with Clinical Research Coordinators (CRC), CRC Managers, and Clinical Research Nurses (CRNs) to manage daily operations and objectives.

  • Interprets and ensures adherence to institutional, sponsor, and regulatory policies related to clinical trial data collection, management, and reporting.

  • : Manages data collection and transmission via protocol-designated EDC systems or paper case report forms (CRFs).

  • Ensures the integrity of clinical trial data by maintaining precise and detailed research records and addressing queries from monitors.

  • Assists in screening, recruiting, selecting, consenting, and enrolling research subjects in clinical trials.

  • Assists in developing, implementing, and evaluating the quality assurance plan for clinical trials, working with sponsor representatives to address monitoring and audit reports.

  • Maintains professional competencies, including human subject research training, and participates in the development of electronic infrastructure and process improvement efforts.

  • May perform other duties as assigned.


Salary Information:

Commensurate with education and experience


Required Documents to Apply:

List of three Professional References (name, email, business title), Resume, Unofficial/Official Transcript(s)


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:

Annual TB Screening, Criminal Background Check


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:

Kneeling, Reaching, Standing, Stooping, Talking, Walking


Frequent Physical Activity:

Reaching, Standing, Stooping, Talking, Walking


Occasional Physical Activity:

Reaching, Sitting, Stooping


Benefits Eligible:

Yes

Average salary estimate

$75000 / YEARLY (est.)
min
max
$60000K
$90000K

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 Data Coordinator, UASYS

Are you ready to make a difference in the world of oncology research? The University of Arkansas for Medical Sciences (UAMS) is looking for a dedicated Clinical Data Coordinator to join our team in Little Rock. In this role, you'll be at the forefront of supporting clinical trials, ensuring the integrity of data collection and entry for various studies. You'll work closely with Clinical Research Coordinators, managers, and nurses, helping to drive projects that improve patient care and support groundbreaking research. With responsibilities ranging from maintaining compliance with regulatory standards to organizing complex data management tasks, your attention to detail will be key. We believe in fostering a collaborative environment, so your communication skills will shine as you engage with diverse stakeholders. If you have at least a Bachelor’s degree and a passion for clinical research, we want to hear from you! Joining us means not only embarking on a rewarding career but also enjoying fantastic benefits like health plans, work-life balance, and ongoing professional development opportunities. Let’s work together to improve the lives of Arkansans and beyond!

Frequently Asked Questions (FAQs) for Clinical Data Coordinator Role at UASYS
What are the responsibilities of a Clinical Data Coordinator at UAMS?

As a Clinical Data Coordinator at the University of Arkansas for Medical Sciences, your main responsibilities include managing data collection and entry for oncology clinical trials. You will ensure adherence to good clinical research documentation practices according to ALCOA+C principles, communicate effectively with team members, and assist with the daily operations of clinical research projects.

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What qualifications are needed for the Clinical Data Coordinator position at UAMS?

To qualify for the Clinical Data Coordinator role at UAMS, candidates typically need a Bachelor's degree along with two years of relevant experience in project management or data collection. Alternatively, an Associate's degree plus four years of relevant experience or a high school diploma plus six years of related experience may also be acceptable.

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What skills are beneficial for a Clinical Data Coordinator at UAMS?

Successful Clinical Data Coordinators at the University of Arkansas for Medical Sciences often possess skills like strong verbal and written communication, the ability to organize and prioritize tasks effectively, familiarity with medical terminology, and experience with data analysis and summarization.

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What are the career growth opportunities for Clinical Data Coordinators at UAMS?

At UAMS, Clinical Data Coordinators can expect numerous opportunities for professional growth and development, including access to training programs, education discounts, and participation in quality assurance initiatives, which could lead to advancement in clinical research roles.

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What benefits can a Clinical Data Coordinator expect at UAMS?

The University of Arkansas for Medical Sciences offers a robust benefits package for Clinical Data Coordinators, including health insurance, retirement contributions, generous paid leave, and educational opportunities for both staff and dependents, enhancing both well-being and career advancement.

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Common Interview Questions for Clinical Data Coordinator
Can you describe your experience with data management in clinical trials?

When answering this question, discuss specific projects where you played a vital role in data collection and management, highlighting your familiarity with clinical research processes and your attention to detail in maintaining data integrity.

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How do you ensure accuracy and compliance when handling clinical trial data?

Illustrate your understanding of ALCOA+C principles and describe methods you use to assure data quality, such as regular audits, peer reviews, and cross-checking with source documents.

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What strategies do you employ to communicate effectively with a diverse team?

Talk about your approach to teamwork, including how you adapt your communication style to different audiences, whether they are clinical staff, research teams, or stakeholders, ensuring clarity and collaboration.

Join Rise to see the full answer
Describe a time when you had to manage a complicated data entry task. How did you handle it?

Share a specific example where you organized complex data efficiently, detailing steps you took to break down tasks, prioritize efficiently, and ensure quality output under tight deadlines.

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What role does technology play in your daily tasks as a Clinical Data Coordinator?

Here, emphasize your proficiency with various data management systems and software such as EDC systems and spreadsheets, explaining how technology enhances your ability to collect, analyze, and report clinical data effectively.

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How do you handle high-pressure situations and tight deadlines?

Provide insight into your stress management techniques that allow you to maintain focus and productivity, such as prioritization, time management, and seeking team support when needed.

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What do you know about the regulatory environment affecting clinical trials?

Showcase your knowledge of regulatory bodies, guidelines, and ethical considerations that govern clinical trials, demonstrating your preparedness to comply with these standards in your role.

Join Rise to see the full answer
In your opinion, what is the most important quality for a Clinical Data Coordinator?

Discuss traits like meticulous attention to detail, strong organizational skills, and effective communication as vital qualities that ensure success in coordinating clinical data.

Join Rise to see the full answer
How would you approach the training of new team members on data entry procedures?

Highlight your willingness to share your knowledge and experience by developing training materials, conducting workshops, and mentoring newcomers to ensure they understand essential processes.

Join Rise to see the full answer
What motivates you to work in clinical research, particularly in oncology?

Convey your passion for making a difference in patient outcomes and contributing to scientific advancements in oncology, tying in personal experiences that underscore your commitment to this field.

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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
April 4, 2025

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