Clinical Trial Manager Jobs in Arizona
A Clinical Trial Manager in the biotechnology industry oversees the planning, implementation, and completion of clinical trials. They are crucial in ensuring that trials are conducted in a way that ensures patient safety, data integrity, and regulatory compliance. They manage budgets, timelines, resources, vendors, and staff involved in the clinical trial, and also handle data management and reporting. They are also responsible for protocol development, site management, and monitoring the study's progress by coordinating with the clinical research associates.
Key skills for a Clinical Trial Manager include strong leadership, project management, and communication abilities. They should also be proficient in medical terminology and have a strong understanding of Good Clinical Practices (GCP), as well as FDA and ICH regulations. A degree in life sciences, nursing or related field, certification like Certified Clinical Research Professional (CCRP) or Certified Clinical Data Manager (CCDM) are often required. Prior roles before becoming a Clinical Trial Manager might include Clinical Research Associate, Clinical Data Coordinator, or Clinical Project Coordinator.
Maintain regulatory documents and IRB correspondence according to Carondelet Standard Operating Procedures, Sponsor specifications and Good Clinical Practice....
Strong scientific and clinical research knowledge is required....
Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements....
Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident...
(Required) Experience One year of clinical research experience or equivalent clinical research training program approved by Director, Clinical Research Operations (Required) Certifications ACRP or SOCRA...
The Clinical Research Coordinator II provides for the safety of patients involved in clinical trials ensuring protocol adherence....
The clinical research coordinator will work on studies focused on meditation and a brain stimulation technique called trans-cranial focused ultrasound....
You will be responsible for independently conducting complex interventional & therapeutic protocols in compliance with FDA regulations and ICH-GCP guidelines....
Research, Regulatory Affairs, Phase I, Phase II, Phase III, Good Clinical Practice, GCP, Regulatory, Clinical Trial Management System, CTMS, IRB, Institutional Review Board, CRMO, Disease Groups, Patient...
Clinical Research Coordinator - Phoenix Vascular Access Center
- Phoenix, AZ
- 20 days ago
- Phoenix, AZ
- 20 days ago
Preferred Certificates and Licenses: Clinical Research EDC, GCP, and IATA training certificates; knowledge of ICH guidelines, GCP, and the clinical trial study process Excellent patient care skills...
Preferred Certificates and Licenses: Clinical Research EDC, GCP, and IATA training certificates; knowledge of ICH guidelines, GCP, and the clinical trial study process Excellent patient care skills...
While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role...
Ensures clinical trial files are documented in accordance with company standard operating procedures, study protocol, and Good Clinical Practice (GCP)....
Prepare and manage Institutional Review Board (IRB) submissions, including responding to stipulations from ancillary review committees for new studies and modifications....
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Salary for Clinical Trial Manager Jobs in Arizona
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Arizona offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Institutional Review Board
- ICH GCP
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Cancer Research
- Medical Affairs
- Drug Development
- Biology
- Scientific Research
- Site Management
- Medical Writing
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Medical Device Sales
- Public Health
- Data Collection
- Patient Care
- Standard Operating Procedures
- Phlebotomy
- Data Management
- Medical Terminology
- Health Care
- Affirmative Action
- Collections
- Quality Control
- Military Background
- Investigation
- Written Communication
- Auditing
- Documentation
- Quality Assurance
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Bachelor's Degree
- Regulations
- Policy Development
- Project Management
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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