Clinical Research Manager Jobs in Arizona
A Clinical Research Manager plays a pivotal role in the biotechnology industry by overseeing and managing clinical trials. They are responsible for creating and implementing trial protocols, ensuring compliance with legal and ethical standards, coordinating with various internal and external stakeholders, and overseeing data collection, management, and analysis. They also monitor the progress of clinical studies and ensure they are completed on time and within budget, while maintaining patient safety and data integrity.
Key skills and certifications for this role include a robust knowledge of Good Clinical Practice (GCP) guidelines, strong analytical and project management skills, and excellent communication abilities. A Clinical Research Manager may also need certifications such as Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Prior to becoming a Clinical Research Manager, an individual might have roles such as Clinical Research Associate or Clinical Research Coordinator, which provide the essential experience in clinical trial conduct and management.
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 Research Manager Jobs in Arizona
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in Arizona offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research 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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