Clinical Trial Manager Jobs in Delaware
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.
Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator...
Life Sciences Senior Project Manager Job ID 221738 Posted 23-May-2025 Service line PJM Segment Role type Full-time Areas of Interest Construction, Project Management Location(s) Newark - Delaware...
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Salary for Clinical Trial Manager Jobs in Delaware
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Delaware offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Report Generation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biostatistics
- Scientific Research
- Specimen Processing
- Urine Testing
- Drug Development
- Medical Writing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Medical Terminology
- Collections
- Military Background
- Auditing
- Investigation
- Presentation
- Education Experience
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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