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Work Study Ccrp Certification Jobs (NOW HIRING)

UAB

MANAGER-CLINICAL RESEARCH COORDINATION

Tampa, FL · On-site

$77K - $126K/yr

To prepare study budgets. * To manage research staff within area including all applicable human ... Work experience may NOT substitute for education requirement. Certified Clinical Research ...

Northwestern University

Work-Study Assistant

Evanston, IL · On-site

$11/hr

Reporting to the Assistant Director, Work-Study Coordinator, the Work-Study Assistant supports the ... Miscellaneous Performed other duties Minimum Qualifications (Education, Experience, Certifications ...

UAB

CLINICAL RESEARCH ADMINISTRATOR III

Tampa, FL · On-site

$55K - $89K/yr

Work experience may NOT substitute for education requirement. Certified Clinical Research ... Professional (CCRP) certification preferred. UAB is an Equal Employment/Equal Educational ...

Dallas College

Work Study Position-1

Farmers Branch, TX · On-site

$15/hr

Federal work study can be on campus or off campus. If on campus you will usually work for your ... You must be enrolled and certified in at least six hours (half time) for Fall and Spring. If ...

McMurry University

Work Study - Peer Tutor

Abilene, TX · On-site

$11.25 - $15/hr

The S3C tutoring program at McMurry University is a CRLA certified program; therefore, each tutor ... Eligibility Applicant must be enrolled as a full-time McMurry student with work study funding ...

Dallas College

Work Study Position-1

Brookhaven, GA

$15/hr

Federal work study can be on campus or off campus. If on campus you will usually work for your ... You must be enrolled and certified in at least six hours (half time) for Fall and Spring. If ...

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Study Management: * Ensure that study activities are conducted in accordance with GCP, IRB ... CCRC/CCRP certification a plus. Why Join Denali Health: * Work with a mission-driven team advancing ...

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Work Study Ccrp Certification information

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$22K

$54.9K

$80.5K

How much do work study ccrp certification jobs pay per year?

As of Jul 28, 2026, the average yearly pay for work study ccrp certification in the United States is $54,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $62,500.00 per year, depending on experience, location, and employer.

Can I use my work-study money for anything?

Work-study funds are typically designated for educational expenses such as tuition, books, supplies, and sometimes limited work-related costs. They are not intended for personal or non-educational expenses outside of approved work activities. The specific use of funds depends on the program's guidelines and the employer's policies.

What is the difference between Work Study Ccrp Certification vs Clinical Research Coordinator Certification?

AspectWork Study Ccrp CertificationClinical Research Coordinator Certification
Required CredentialsCCRPs, work-study eligibility, relevant courseworkCCRPs, experience in clinical research, specific training
Work EnvironmentAcademic settings, research labs, hospitalsClinical trial sites, hospitals, research organizations
Employer & Industry UsageUniversities, research institutions, hospitalsPharmaceutical companies, CROs, hospitals
Common Search & Comparison IntentUnderstanding certification for student roles in researchCertifications for clinical research coordinators

Work Study CCRP Certification is typically aimed at students involved in research projects, focusing on foundational knowledge and academic settings. In contrast, Clinical Research Coordinator Certification is designed for professionals managing clinical trials, requiring more extensive experience and specific industry credentials. Both certifications support careers in clinical research but serve different roles and career stages.

How do you get a work-study job?

To get a work-study job, students must complete the Free Application for Federal Student Aid (FAFSA) and indicate interest in work-study programs. Once approved, students can search for available positions on their school's job portal, which often involve on-campus roles requiring basic skills and adherence to a set schedule.

What is a work-study job?

A work-study job is a part-time position offered to students as part of a financial aid program, allowing them to earn money to help pay for education expenses. These jobs are typically on-campus or related to the student's field of study and often require eligibility through a work-study award. The position helps students gain work experience while balancing academic responsibilities.

What jobs can you get with a vocational certificate?

A Work Study CCRP Certification can qualify individuals for roles such as clinical research coordinator, laboratory technician, or healthcare assistant. These jobs often require knowledge of research protocols, data management, and compliance with regulatory standards, and they are typically found in healthcare, research facilities, or clinical settings.
What cities are hiring for Work Study Ccrp Certification jobs? Cities with the most Work Study Ccrp Certification job openings:
What are the most commonly searched types of Ccrp Certification jobs? The most popular types of Ccrp Certification jobs are:
What states have the most Work Study Ccrp Certification jobs? States with the most job openings for Work Study Ccrp Certification jobs include:
Work Study Ccrp Certification jobs near you
MANAGER-CLINICAL RESEARCH COORDINATION

MANAGER-CLINICAL RESEARCH COORDINATION

UAB

Tampa, FL • On-site

$77K - $126K/yr

Other

Posted 22 days ago

UAB Medicine rating

7.3

Company rating: 7.3 out of 10

Based on 187 frontline employees who took The Breakroom Quiz

306th of 890 rated healthcare providers

Job description

The University of Alabama at Birmingham (UAB), Department of Med - Cardiovascular Disease, is seeking a Manager-Clinical Research Coordination.

General Responsibilities

  • To manage all aspects of research program and clinical studies including education/teaching.

  • To oversee and manage multiple clinical research protocols and the associated personnel.

  • To design best practices for management of IP for drug, device, and biologic studies.

  • To prepare study budgets.

  • To manage research staff within area including all applicable human resources functions.

Key Duties & Responsibilities

  1. Provides leadership and operational oversight for a complex clinical research program involving multiple clinical studies and research personnel.

  2. Serves as a key resource for faculty, sponsors, and research staff, ensuring studies are conducted in compliance with institutional, sponsor, federal, and regulatory requirements.

  3. In addition to managing study operations, this role is responsible for supervising and mentoring research staff, driving quality improvement initiatives, overseeing clinical trial management systems, and conducting quality assurance activities.

  4. The position offers an opportunity to influence research operations, develop best practices, and contribute to the growth and success of the CCTU.

  5. The ideal candidate will have significant experience managing clinical research operations, staff, and regulatory compliance in a complex academic medical center, healthcare, or research environment.

  6. Performs other duties as assigned.

Annual Salary Range:   $77,640 - $126,170

Bachelor's degree in a related field and eight (8) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred.

Preferences

  • Degree in Clinical Research, Public Health, etc.

  • Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred.

Preferred Hard Skills: Clinical research operations management, Knowledge of FDA regulations, ICH-GCP guidelines, and human subject research protections. Experience managing multisite and/or industry-sponsored clinical trials. Experience with Clinical Trial Management Systems (CTMS), such as OnCore. Experience with Electronic Data Capture (EDC) systems Quality assurance, auditing, and regulatory compliance oversight. Research program development and process improvement. SOP development and implementation. Project management. Experience with institutional research systems such as IRAP and OnCore.

Preferred Soft Skills: Leadership and staff development. Staff training and competency development. Coaching, mentoring, and training. Strategic thinking and problem-solving. Excellent organizational and prioritization skills. Strong written and verbal communication skills. Collaboration and relationship building with faculty, sponsors, and interdisciplinary teams. Conflict resolution and performance management. Ability to manage multiple competing priorities in a fast-paced environment.
 

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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