Top 37 Trial manager Jobs in Tucson, Az

Clinical Research Coordinator I - Nurse
Iterative Health —Tucson, AZ
- Nursing
- RN License
- Quality control
Quick Apply
Store Worker Leader
US Defense Commissary Agency —Davis-Monthan AFB, AZ
- $24.62 - $28.73 an hour
- Part-time
- Background check
- 18 years or older
- Management
7d
Store Associate
US Defense Commissary Agency —Davis-Monthan AFB, AZ
- $17.82 - $23.11 an hour
- Overtime
- Background check
- 18 years or older
- Pass drug screening
Research Quality Compliance (QC) Coordinator
Arizona Liver Health —Tucson, AZ
- $60,000 - $75,000 a year
- Full-time
- Computer literacy
- Mid-level
- Master's degree
- Mileage reimbursement
- Health savings account
9h
Escrow Assistant I
Agave Title Agency —Tucson, AZ
- Writing skills
- Office
- Administrative experience
- Health savings account
- Health insurance
Supervisory IT Specialist (Area Manager)
US Deputy Assistant Secretary for Information and Technology —Tucson, AZ
- $128,162 - $166,615 a year
- Online Application
- Background check
- Psychiatry
- Pass drug screening
2d
Transportation Security Officer
US Transportation Security Administration —Tucson, AZ
- $41,508 - $57,922 a year
- Overtime
- Background check
- 18 years or older
- Ability to walk for extended periods
- Travel reimbursement
- Paid holidays
Commissary Contractor Monitor
US Defense Commissary Agency —Davis-Monthan AFB, AZ
- $46,270 - $60,151 a year
- Part-time
- Background check
- 18 years or older
- Inventory management
5d
Project Manager - Mine Closure (GeoSystems Analysis)
Westland Resources —Tucson, AZ
- $115,000 - $150,000 a year
- Full-time
- Microsoft Word
- Spanish
- Microsoft Excel
- Paid holidays
- Health insurance
Quick Apply
7d
Medical Supply Tech (Sterile Processing)
US Veterans Health Administration —Tucson, AZ
- $52,199 - $75,642 a year
- Online Application
- Background check
- Anatomy knowledge
- Surgery
Contract Specialist
University of Arizona —Tucson, AZ
- $59,404 - $74,254 a year
- Full-time
- Hybrid work
- Mid-level
- Residential
- 3 years
- Paid holidays
- Health insurance
Sales Store Checker
US Defense Commissary Agency —Davis-Monthan AFB, AZ
- $17.47 - $21.46 an hour
- Overtime
- Background check
- 18 years or older
- Customer service
Meatcutting Worker
US Defense Commissary Agency —Davis-Monthan AFB, AZ
- $20.82 - $24.29 an hour
- Overtime
- Background check
- 18 years or older
- Pass drug screening
Project Engineer
FLSmidth, Inc. —Tucson, AZ
- Full-time
- Microsoft Word
- Management
- English
- Disability insurance
- Health insurance
Strategic Sourcing Specialist
FLSmidth, Inc. —Tucson, AZ
- Full-time
- 5 years
- ERP systems
- English
Manager Clinical Research - TMCH Cancer Center
Tucson Medical Center —Tucson, AZ
- Full-time
- Nursing
- RN License
- 5 years
Clinical Research Coordinator II
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC —Tucson, AZ
- Private practice
- Mid-level
- Office
Quick Apply
2d
Director Clinical Trials Administration
Tucson Medical Center —Tucson, AZ
- Full-time
- Nursing
- Microsoft Outlook
- HIPAA
9d
Staff Psychologist (Women's Health)
US Veterans Health Administration —Tucson, AZ
- $107,176 - $184,398 a year
- Online Application
- Background check
- Doctoral degree
- Pass drug screening
- Paid parental leave
- Loan repayment program
12d
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Tucson, AZ
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification

I want to receive the latest job alert for trial manager in tucson, az

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

trial manager jobs near tucson, az

Clinical Research Coordinator I - Nurse

Iterative Health -
Tucson, AZ

Quick Apply

Job Details

Qualifications

RN License

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

A Clinical Research Coordinator I – RN at Iterative Health is an essential member of the site research team, supporting, facilitating, and coordinating the daily execution of clinical trials across our network. This role is at the heart of every study — managing patient interactions, ensuring protocol compliance, maintaining data integrity, and keeping the operational machinery of clinical research running smoothly.

The ideal candidate brings clinical research experience, a patient-first mindset, strong attention to detail, and the ability to thrive in a fast-paced, protocol-driven environment. This role provides a strong foundation for success while offering a clear path for professional growth within Iterative Health's expanding site network.

Where You'll Drive Impact

Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
Schedule all patient research visits and procedures in accordance with protocol requirements.
Ensure relevant study and subject-specific information is entered into the CTMS on a regular basis.
Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
Schedule and prepare for monitor visits.
Maintain inventory of study equipment and supplies onsite at all times.

Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.
Conduct patient visits as outlined within each study protocol.
Act as the primary point of contact for study participants throughout the course of the study.

Dispense study medication, collect vital signs, and perform ECGs per protocol.
Perform blood draws; process and ship specimens per study protocol and IATA regulations.
As assigned: place IVs, administer IV medications and fluids, give intramuscular and subcutaneous injections, monitor patients during infusion, and discharge patients in accordance with protocol and site policies.

Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.
Ensure all safety data is reviewed by the PI in a timely manner.
Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study.
Actively participate in communication of status and results to management.

Perform job related duties as requested

What You Bring to the Team

Active Registered Nurse (RN) license required.
1–2 years of clinical research experience strongly preferred .
Solid nursing background with a concentration in, or willingness to develop advanced knowledge of, GI specialty.
Ability to execute research tasks with guidance from experienced staff, PIs, and management.
Strong written and verbal communication skills.
Ability to read, interpret, and apply clinic policies and research protocols.
Proficiency in standard office software and CTMS platforms.
Highly organized with the ability to manage multiple priorities and meet deadlines.
Ability to work independently and collaboratively in a fast-paced environment.

Preferred Qualifications

Prior GI or hepatology clinical research experience.
Familiarity with GCP guidelines and FDA regulations governing clinical research.
Experience with CTMS, EDC, or eTMF platforms.
ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification.

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

Quick Apply

Refine Your Search

trial manager jobs in tucson, az

Clinical Research Coordinator I - Nurse

Store Worker Leader

Store Associate

Research Quality Compliance (QC) Coordinator

Escrow Assistant I

Supervisory IT Specialist (Area Manager)

Transportation Security Officer

Commissary Contractor Monitor

Project Manager - Mine Closure (GeoSystems Analysis)

Medical Supply Tech (Sterile Processing)

Contract Specialist

Sales Store Checker

Meatcutting Worker

Project Engineer

Strategic Sourcing Specialist

Manager Clinical Research - TMCH Cancer Center

Clinical Research Coordinator II

Director Clinical Trials Administration

Staff Psychologist (Women's Health)

Per Diem Clinical Research Nurse - Home Visits

I want to receive the latest job alert for trial manager in tucson, az

Related Searches

Explore jobs in more locations

Where You'll Drive Impact

Preferred Qualifications

Job Seeker Tools

Employer Tools

Browse

Stay Connected