Clinical Trial Manager Jobs in Tucson, AZ
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.
Assists in regulatory functions, including but not limited to preparing appropriate Institutional Review Board (IRB) forms, processing updated informed consents, protocols, correspondence, and regulatory...
In PersonPrevious clinical research experience....
In PersonClinical Research Coordinator I, Family and Community Medicine (Full Time)
- University of Arizona
- Tucson, AZ
- 8 days ago
- Tucson, AZ
- 8 days ago
Submits project protocols and amendments, consent forms, and recruiting materials to the University of Arizona Institutional Review Board and department for approval with oversight from supervisor....
In Person Full TimeClinical Research Coordinator II
- University of Arizona
- Tucson, AZ
- 12 days ago
- Tucson, AZ
- 12 days ago
Creating source documents, study specific training in accordance with study protocols and Good Clinical Practice (GCP) guidelines....
In PersonClinical Research Coordinator I
- Tucson Medical Center
- Tucson, AZ
- 30+ days ago
- Tucson, AZ
- 30+ days ago
The Clinical Research Coordinator I (CRC I) promote good clinical practices in the conduct of investigations by possessing an in-depth knowledge of federal regulations and guidance documents for the...
In Person Full TimeTEMPORARY - Clinical Research Coordinator - Tucson
- Arizona Liver Health
- Tucson, AZ
- 30+ days ago
- Tucson, AZ
- 30+ days ago
Ensure study compliance with Good Clinical Practice (GCP), FDA, ICH, or other applicable regulatory guidelines....
In Person TemporaryThe Travel Clinical Research Coordinator is proficient at ICH/GCP, Good Documentation Practices (GDP), and ALCOA-C+....
In PersonClinical Research Coordinator II (CRC2) Tucson
- Arizona Liver Health
- Tucson, AZ
- 45+ days ago
- Tucson, AZ
- 45+ days ago
Record data and study documentation Keep the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators and...
In PersonClinical Research Coordinator III - Arthritis Center
- University of Arizona
- Tucson, AZ
- 60+ days ago
- Tucson, AZ
- 60+ days ago
Maintain regulatory and study documentation in accordance with policies and regulations of University of Arizona Institutional Review Board (IRB), National Institute of Health, and other relevant organizations...
In PersonDemographic Data for Tucson, AZ
Moving to Tucson, AZ? Find some basic demographic data about Tucson, AZ below.
Clinical Trial Manager Online Courses and Training Opportunities
Title Synonyms
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Salary for Clinical Trial Manager Jobs in Tucson, AZ
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Tucson, AZ offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Budgets
- Good Clinical Practice
- ICH Guidelines
- Study Management
- Institutional Review Board
- Clinical Monitoring
- Biomarkers
- ICH GCP
- Clinical Trial Management System
- Drug Development
- Clinical Data Management
- Scientific Research
- Gene Therapy
- Cancer Research
- Biology
- Site Management
- Clinical Trials
- Specimen Collection
- Clinical Operations
- Clinical Research
- Biotechnology
- Neuroscience
- Neurology
- Medical Device Sales
- Venipuncture
- FDA Regulations
- Oncology
- Data Collection
- Standard Operating Procedures
- Patient Care
- Phlebotomy
- Data Management
- Medical Terminology
- Health Care
- Collections
- Quality Control
- Auditing
- Written Communication
- Investigation
- Documentation
- Interpersonal Skills
- Implementation
- Reporting
- Data Entry
- Collaboration
- Education Experience
- Bachelor's Degree
- Regulations
- Research Skills
- Microsoft Excel
- Microsoft Office
- Project Management
- Problem Solving
- Staff Supervision
- Scheduling
- Leadership
- Communication Skills
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