Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
Clinical Research Coordinator
$24 - $31.75/hr
... trials. You're not afraid to pick up the phone to screen a patient for a new study and by the time you're done the two of you are BEST buds. * How to effectively manage your time when there is a lot ...
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Clinical Research Coordinator
$24 - $31.75/hr
... trials. You're not afraid to pick up the phone to screen a patient for a new study and by the time you're done the two of you are BEST buds. * How to effectively manage your time when there is a lot ...
Lead implementation of regulatory strategy for institutionally sponsored clinical trials, including ... Trial Startup, Lifecycle Management, and Sponsor Oversight:Lead sponsor regulatory and compliance ...
Lead implementation of regulatory strategy for institutionally sponsored clinical trials, including ... Trial Startup, Lifecycle Management, and Sponsor Oversight:Lead sponsor regulatory and compliance ...
Clinical Research Pain Management Tucson, AZ, | ⏰ Part-Time (0-8 hours/week) About the Role We ... Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ...
Clinical Research Pain Management Tucson, AZ, | ⏰ Part-Time (0-8 hours/week) About the Role We ... Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ...
... trials virtually or in-person. Operational Strategy - Analyze litigation trends to reduce legal spend.- Develop best practices for TPA data reporting.- Collaborate with internal risk management and ...
... trials virtually or in-person. Operational Strategy - Analyze litigation trends to reduce legal spend.- Develop best practices for TPA data reporting.- Collaborate with internal risk management and ...
You will manage outside defense counsel, drive litigation strategies, and ensure TPAs adhere to ... Attend high-exposure mediations and trials virtually or in-person. Operational Strategy * Analyze ...
You will manage outside defense counsel, drive litigation strategies, and ensure TPAs adhere to ... Attend high-exposure mediations and trials virtually or in-person. Operational Strategy * Analyze ...
CRC Operations Lead (31535)
Peoria, AZ · On-site
Manage assigned clinical trials end-to-end, including participant visits, data collection, source documentation, and sponsor relations. * Able to manage multiple studies with varying indications.
CRC Operations Lead (31535)
Peoria, AZ · On-site
Manage assigned clinical trials end-to-end, including participant visits, data collection, source documentation, and sponsor relations. * Able to manage multiple studies with varying indications.
Clinical Trials Budget Analyst III
Phoenix, AZ · On-site +1
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Clinical Trials Budget Analyst III
Phoenix, AZ · On-site +1
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Clinical Research Assistant (CRA)
Gilbert, AZ · On-site
$38K - $48K/yr
Lighthouse Psychiatry is seeking a Clinical Research Assistant (CRA) (Psychiatry) to manage and support psychiatric and CNS clinical trials in an outpatient setting. This role oversees day-to-day ...
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Clinical Research Assistant (CRA)
Gilbert, AZ · On-site
$38K - $48K/yr
Lighthouse Psychiatry is seeking a Clinical Research Assistant (CRA) (Psychiatry) to manage and support psychiatric and CNS clinical trials in an outpatient setting. This role oversees day-to-day ...
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Quick apply
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Clinical decision making & management of patients in trials. * Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols. * Recruit, screen, and ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Preferred EXPERIENCE * 5 years Progressively responsible experience in clinical research budgeting, contracting, or financial management. Required * Expertise with complex or multi-arm clinical trial ...
Physician - Internist
$250K - $300K/yr
Serve as the Principal Investigator (PI) for clinical trials related to the treatment and management of multi-organ diseases. * Ensure clinical trials comply with regulatory requirements, ethical ...
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Physician - Internist
$250K - $300K/yr
Serve as the Principal Investigator (PI) for clinical trials related to the treatment and management of multi-organ diseases. * Ensure clinical trials comply with regulatory requirements, ethical ...
Physician - Internist
Chandler, AZ · On-site
$250K - $300K/yr
Serve as the Principal Investigator (PI) for clinical trials related to the treatment and management of multi-organ diseases. * Ensure clinical trials comply with regulatory requirements, ethical ...
Physician - Internist
Chandler, AZ · On-site
$250K - $300K/yr
Serve as the Principal Investigator (PI) for clinical trials related to the treatment and management of multi-organ diseases. * Ensure clinical trials comply with regulatory requirements, ethical ...
Trials Manager information
What are the key skills and qualifications needed to thrive as a trials manager, and why are they important?
To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.
What is a trials manager?
Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.
What are the main challenges a trials manager faces when coordinating multi-site clinical trials?
As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.
What is the difference between Trials Manager vs Clinical Research Coordinator?
| Criteria | Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in trial management, knowledge of regulations | Bachelor's degree, clinical research experience, regulatory knowledge |
| Work Environment | Oversees multiple trials, manages teams, coordinates with sponsors | Handles daily trial activities, patient interactions, data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.
What are popular job titles related to Trials Manager jobs in Arizona? For Trials Manager jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Trials Manager jobs in Arizona look for? The top searched job categories for Trials Manager jobs in Arizona are:
What cities in Arizona are hiring for Trials Manager jobs? Cities in Arizona with the most Trials Manager job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 223 rated it services
Job description
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
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
Job Overview- 2+ years of global study management experience
- Experience across multiple countries/regions
- Phase I-III clinical trials experience (Phase III required)
- Oncology experience required
- Ability to work across multiple therapeutic areas
We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout-while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.
Key ResponsibilitiesGlobal Study & Site Leadership- Lead site management strategy from study award through close-out
- Oversee site identification, selection, activation, and recruitment performance
- Ensure clinical monitoring processes meet study needs and timelines
- Partner with CRAs to optimize enrollment, data quality, and compliance
- Serve as primary client contact and own key customer relationships
- Lead cross-functional teams across regions and cultures
- Facilitate internal and external meetings, including executive presentations
- Drive collaboration across stakeholders, vendors, and functional leads
- Develop and manage integrated study plans and risk mitigation strategies
- Proactively identify risks and implement corrective/preventative actions
- Monitor study timelines, enrollment trends, and data quality metrics
- Ensure compliance with GCP, SOPs, protocols, and regulatory standards
- Manage study financials, including forecasting and revenue acceleration
- Identify and manage out-of-scope work and change orders
- Oversee Billing Unit Reviews (BURs) and expense approvals
- Track performance against budget and Estimate at Completion (EAC)
- Maintain TMF health and ensure timely document submission
- Develop quality monitoring plans and compliance metrics
- Ensure adherence to study tools, training materials, and processes
- Lead and mentor cross-functional project teams
- Support CRA and team training on therapeutic areas and study-specific needs
- Foster collaboration, knowledge sharing, and continuous improvement
- Bachelor's degree in life sciences or related field
- 5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
- Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
- Experience managing global clinical trials and multi-regional teams
- Demonstrated experience in project financial management
- Exceptional communication and stakeholder management skills
- Strong problem-solving and risk mitigation capabilities
- Ability to influence without authority in matrix organizations
- High attention to detail and quality-driven mindset
- Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)
- Work on cutting-edge global trials across therapeutic areas
- Collaborate with top talent in a dynamic, global environment
- Make a direct impact on patient outcomes worldwide
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US