Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials. * Conduct medical screenings, dermatological assessments, and physical ...
Quick apply
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials. * Conduct medical screenings, dermatological assessments, and physical ...
Quick apply
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials. * Conduct medical screenings, dermatological assessments, and physical ...
Tucson, AZ · On-site
$100 - $125/hr
These trials can be observational, where a group is simply studied without intervention, or clinical, where an intervention is applied to some or all of the participants. According to the US National ...
Tucson, AZ · On-site
$100 - $125/hr
These trials can be observational, where a group is simply studied without intervention, or clinical, where an intervention is applied to some or all of the participants. According to the US National ...
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
Quick apply
DR The Recruitment Specialist plays a key role in supporting patient enrollment for ongoing clinical trials. You are the frontline in connecting potential participants to important research ...
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
New
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
New
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Quick apply
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Phoenix, AZ · Hybrid
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Phoenix, AZ · Hybrid
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Scottsdale, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
New
Scottsdale, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
New
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
Phoenix, AZ · On-site
Manages all assigned clinical trials unblinded pharmacy responsibilities * Travels to sites approximately 3 days per week to prepare investigational medication * Responsible for preparation of ...
$23.25 - $31/hr
The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with ...
Quick apply
$23.25 - $31/hr
The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with ...
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Quick apply
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor-specified timelines * Build imaging protocols and perform scans across ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Tucson, AZ · On-site
$23 - $30.50/hr
Maintain retention by following up with participants in long-term clinical trials. * Gather consent forms for approval by Human Subjects Panel. * Complete study data entry in various electronic data ...
Tucson, AZ · On-site
$23 - $30.50/hr
Maintain retention by following up with participants in long-term clinical trials. * Gather consent forms for approval by Human Subjects Panel. * Complete study data entry in various electronic data ...
| Aspect | Weekend Clinical Trials | Part-Time Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires clinical trial experience, basic medical knowledge | Requires certification in clinical research or related field, experience preferred |
| Work Environment | Conducted at research sites, hospitals, or clinics during weekends | Office-based, overseeing trial activities, often flexible hours |
| Employer & Industry | Pharmaceutical companies, research organizations, hospitals | Research institutions, hospitals, clinical trial sites |
| Search & Comparison Intent | Understanding weekend trial roles, flexible clinical trial work | Part-time research coordination, clinical trial management |
Weekend Clinical Trials involve participating in or managing clinical studies during weekends, often at research sites. Part-Time Clinical Research Coordinators oversee trial activities, ensuring compliance and data collection, usually during regular hours but on a part-time basis. Both roles support clinical research but differ in schedule, responsibilities, and required credentials.
The most popular types of Clinical Trials jobs in Arizona are:
Cities in Arizona with the most Weekend Clinical Trials job openings:
Job Title: Clinical Research Endocrinologist
Location: Glendale, AZ
Schedule: Part-Time (0-8 hours)
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials.
Conduct medical screenings, dermatological assessments, and physical examinations for study participants.
Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements.
Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation.
Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs.
Participate in site initiation visits (SIVs), monitoring visits, and audits.
Contribute to protocol feasibility reviews, study design input, and recruitment strategies.
Attend investigator meetings and provide medical expertise on dermatology-related endpoints and safety monitoring.
Stay current on clinical research regulations and advances in dermatology and investigational therapies.
M.D. or D.O. with an active, unrestricted Arizona medical license.
Board certification in Endocrinologist required.
Valid DEA license and BLS/ACLS certification.
Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates).
Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
Strong interpersonal and communication skills with the ability to work in a multidisciplinary, fast-paced environment.
Commitment to ethical research practices and patient-centered care.
Sourced by ZipRecruiter
Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.
Recruiting and staffing services
51 - 200 Employees
Frisco, TX, US
1989