Top 119 Site manager Jobs in Tucson Az

Clinical Research Coordinator I - Nurse
Iterative Health —Tucson, AZ
- Nursing
- RN License
- Quality control
Quick Apply
Principal Sensor Calibration Lead
Raytheon —Tucson, AZ
- $107,500 - $204,500 a year
- Full-time
- Management
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Site Manager - Travel Foreman
HJ3 Composite Technologies —Tucson, AZ
- $55,000 - $75,000 a year
- Full-time
- Hybrid work
- Background check
- Clean driving record
- Construction site
- Health insurance
- Dental insurance
Quick Apply
Sr Principal Electrical Subsystem Architect
Raytheon —Tucson, AZ
- $132,400 - $251,600 a year
- Full-time
- 7 years
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Lead Construction Project Manager
MIRACORP INC —Tucson, AZ
- $100,000 - $110,000 a year
- Full-time
- Construction site
- Engineering
- 11+ years
- Commuter assistance
- AD&D insurance
Quick Apply
RF Design Engineer II
Raytheon —Tucson, AZ
- $68,900 - $131,100 a year
- Full-time
- Experience equivalent to degree accepted
- In-person
- Senior level
- Paid holidays
- Disability insurance
Principal Engineer – One Shots
Raytheon —Tucson, AZ
- $107,500 - $204,500 a year
- Full-time
- 5 years
- Travel
- Contracts
- Paid holidays
- Disability insurance
Site Manager In Training - Travel Foreman
HJ3 Composite Technologies —Tucson, AZ
- $53,000 - $55,000 a year
- Full-time
- Background check
- Clean driving record
- Construction site
- Health insurance
- Dental insurance
Quick Apply
10d
Principal Engineer – Propulsion
Raytheon —Tucson, AZ
- $107,500 - $204,500 a year
- Full-time
- 5 years
- Travel
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
5d
ACI Certified Field Technician
ZEMLOCK LLC —Tucson, AZ
- $20 - $26 an hour
- Urgently hiring
- Clean driving record
- Construction site
- Laboratory experience
Quick Apply
Senior Principal Engineer – Solid Propulsion
Raytheon —Tucson, AZ
- $132,400 - $251,600 a year
- Full-time
- 7 years
- Travel
- Experience equivalent to degree accepted
- Paid holidays
- Disability insurance
Site Superintendent in Tucson AZ
Fedvet Construction —Tucson, AZ
- $90,000 - $120,000 a year
- Weekends as needed
- Microsoft Word
- Background check
- CPR Certification
Quick Apply
Office Manager
Cloudprinter —Tucson, AZ
- $22 - $28 an hour
- Full-time
- Google Workspace
- English
- Mid-level
Site Review Project Manager I - Development Services
Pima County —Tucson, AZ
- $72,009 - $100,817 a year
- Full-time
- Background check
- Mid-level
- Office
Principal Procurement Specialist
Raytheon —Tucson, AZ
- $86,800 - $165,200 a year
- Full-time
- Remote
- Data analysis skills
- 3 years
- Travel
- Paid holidays
- Disability insurance
4d
Construction Superintendent
G&J Development —Tucson, AZ
- Email
- In person
- Background check
- Clean driving record
- Management
- Fuel card
- Paid holidays
Quick Apply
On-Site Project Manager - Furniture Installations
Storage Scholars —Tucson, AZ
- $250 - $500 a day
- Contract
- Mid-level
- Budgeting
- In-person
Quick Apply
Site Manager
The Homing Project —Tucson, AZ
- From $25 an hour
- Weekends as needed
- Background check
- Spanish
- English
Quick Apply
5d
Construction Superintendent (National Traveling) - Tucson
Horizon Retail Construction —Tucson, AZ
- Full-time
- Microsoft Outlook
- Construction site
- 5 years
- Paid holidays
- Health insurance
Quick Apply
Senior Practice Manager - TMCH Cancer Center
Tucson Medical Center —Tucson, AZ
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy

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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

site manager jobs in tucson az

Clinical Research Coordinator I - Nurse

Principal Sensor Calibration Lead

Site Manager - Travel Foreman

Sr Principal Electrical Subsystem Architect

Lead Construction Project Manager

RF Design Engineer II

Principal Engineer – One Shots

Site Manager In Training - Travel Foreman

Principal Engineer – Propulsion

ACI Certified Field Technician

Senior Principal Engineer – Solid Propulsion

Site Superintendent in Tucson AZ

Office Manager

Site Review Project Manager I - Development Services

Principal Procurement Specialist

Construction Superintendent

On-Site Project Manager - Furniture Installations

Site Manager

Construction Superintendent (National Traveling) - Tucson

Senior Practice Manager - TMCH Cancer Center

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

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