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Study Com Jobs in Tucson, AZ (NOW HIRING)

Manage corridor studies, concept studies, active transportation plans, feasibility studies, and ... com Equal Opportunity Employer including disability and protected veteran status EEO - All ...

Civil Engineer

Tucson, AZ · On-site

$90K/yr

Prepare drainage calculations and reports. Assist with preparation of feasibility studies. Resolve drainage related issues in the field and coordinate with plan reviewers on all matters related to ...

Civil Engineer

Tucson, AZ · On-site

$90K/yr

... studies. • Resolve drainage related issues in the field and coordinate with plan reviewers on all matters related to drainage design. • Coordinate with all disciplines involved (Architectural ...

Senior Transportation Planner

Tucson, AZ · On-site

$120K - $170K/yr

Manage corridor studies, concept studies, active transportation plans, feasibility studies, and ... com Equal Opportunity Employer including disability and protected veteran status EEO - All ...

Senior Transportation Planner

Tucson, AZ · On-site

$120K - $170K/yr

Manage corridor studies, concept studies, active transportation plans, feasibility studies, and ... com Equal Opportunity Employer including disability and protected veteran statusEEO - All qualified ...

Senior Transportation Planner

Tucson, AZ · On-site

$120K - $170K/yr

Manage corridor studies, concept studies, active transportation plans, feasibility studies, and ... com Equal Opportunity Employer including disability and protected veteran statusEEO - All qualified ...

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Study Com information

See Tucson, AZ salary details

$19.7K

$112.1K

$184.4K

How much do study com jobs pay per year?

As of Aug 29, 2026, the average yearly pay for study com in Tucson, AZ is $112,149.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,100.00 and $140,500.00 per year, depending on experience, location, and employer.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What are popular job titles related to Study Com jobs in Tucson, AZ?

For Study Com jobs in Tucson, AZ, the most frequently searched job titles are:

What cities near Tucson, AZ are hiring for Study Com jobs?

Cities near Tucson, AZ with the most Study Com job openings:

Infographic showing various Study Com job openings in Tucson, AZ as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, and 6% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $112,149 per year, or $53.9 per hour.

Clinical Research Coordinator I - Sarver Heart Center (COM-T)

University of Arizona

Tucson, AZ • On-site

$47K - $59K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 6 days ago


University Of Arizona rating

7.3

Company rating: 7.3 out of 10

Based on 68 frontline employees who took The Breakroom Quiz

365th of 627 rated colleges and universities


Job description

Clinical Research Coordinator I - Sarver Heart Center (COM-T)
Posting Number
req25276
Department
Sarver Heart Center
Department Website Link
https://heart.arizona.edu/
Location
Tucson Campus
Address
Tucson, AZ USA
Position Highlights
The Sarver Heart Center is seeking a Clinical Research Coordinator I to support clinical research conducted by University of Arizona faculty. The selected individual will support daily clinical research operations by successfully implementing and adhering to clinical research studies. Clinical research activities will include screening, recruitment, study visit procedures, data collection, and sample processing. This position will require professional communication and collaboration with physicians, hospital partners, and study sponsors.
  • Occasional out-of-state travel may be required for sponsor training. Weekend and evening departmental support may be required to meet study protocol requirements.
Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; U of A/ASU/NAU tuition reduction for the employee and qualified family members; retirement plans; access to U of A recreation and cultural activities; and more!The University of Arizona has been recognized for our innovative work-life programs. For more information about working at the University of Arizona and relocation services, please click here.
Duties & Responsibilities
  • Following detailed instruction, will screen, recruit and enroll participants for assigned studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.
  • Under direction, will inform and instruct study participants concerning research protocol and complete the patient informed consent procedure.
  • Under direction of PI, assist with coordinating and and/or performing research testing per protocol such as drawing blood, vital signs, EKGs, etc., includes processing and packaging of laboratory samples for shipment.
  • With detailed instruction, assess participants during research visit; perform initial review of study lab results; assess for any side effects or other problems; notify principal investigator of any participant reported side effects or problems.
  • With detailed instruction, complete case report forms for each study participant, and document medical data in the patient record and sponsor database. Ensure case report forms or other data collection/tracking tools are created if not provided by sponsor.
  • Assist PI with sponsor site visit and audits for assigned studies, including escorting visitors and providing requested documentation.
  • Provides weekend and evening support for team coordination, communication, etc. to meet study protocol requirements.

Knowledge, Skills, and Abilities:
  • Demonstrated excellence in written and verbal communication.
  • Ability to interpret and analyze data.
  • Demonstrated ability to collaborate effectively with peers, patients, management, and internal and external stakeholders, fostering professional relationships that support operational efficiency, patient-centered service, and cross-functional project success.
  • Knowledge of the principles, practices and techniques of clinical research skills.
  • Proven ability to provide high quality, compliant research and ethical standards.

This job posting reflects the general nature and level of work expected of the selected candidate(s). It is not intended to be an exhaustive list of all duties and responsibilities. The institution reserves the right to amend or update this description as organizational priorities and institutional needs evolve.
Minimum Qualifications
  • Bachelor's degree or equivalent advanced learning attained through experience required.
  • One (1) year of relevant work experience is required.

Preferred Qualifications
  • Bilingual in English and Spanish
  • Experience in Human Subjects research
  • Experience with research protocols, development, and regulations.

FLSA
Exempt
Full Time/Part Time
Full Time
Number of Hours Worked per Week
40
Job FTE
1.0
Work Calendar
Fiscal
Job Category
Research
Benefits Eligible
Yes - Full Benefits
Rate of Pay
$47,356 - $59,195
Compensation Type
salary at 1.0 full-time equivalency (FTE)
Grade
6
Compensation Guidance
The Rate of Pay Field represents the University of Arizona's good faith and reasonable estimate of the range of possible compensation at the time of posting. The University considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, key skills, and internal equity.
The Grade Range represent a full range of career compensation growth over time. The university offers compensation growth opportunities within its career architecture. To learn more about compensation, please review our Applicant Compensation Guide and our Total Rewards Calculator.
Career Stream and Level
PC1
Job Family
Clinical Research
Job Function
Research
Type of criminal background check required:
Name-based criminal background check (non-security sensitive)
Number of Vacancies
2
Target Hire Date
Expected End Date
Contact Information for Candidates
Gerry Flores gflores007@arizona.edu
Open Date
2/24/2026
Open Until Filled
Yes
Documents Needed to Apply
Resume and Cover Letter
Special Instructions to Applicant
Notice of Availability of the Annual Security and Fire Safety Report
In compliance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), each year the University of Arizona releases an Annual Security Report (ASR) for each of the University's campuses.Thesereports disclose information including Clery crime statistics for the previous three calendar years and policies, procedures, and programs the University uses to keep students and employees safe, including how to report crimes or other emergencies and resources for crime victims. As a campus with residential housing facilities, the Main Campus ASR also includes a combined Annual Fire Safety report with information on fire statistics and fire safety systems, policies, and procedures.
Paper copies of the Reports can be obtained by contacting the University Compliance Office at cleryact@arizona.edu.

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