Clinical Research Associate Jobs in Minnesota
A Clinical Research Associate (CRA) plays a pivotal role in the biotechnology industry, overseeing various aspects of clinical trials. These include designing, implementing, and monitoring clinical trials, ensuring data integrity, verifying case report forms, providing progress reports, and ensuring compliance with protocols and regulatory requirements. CRAs play a crucial role in the development, testing, and approval of new products in the biotechnology industry by managing the clinical trials that prove their safety and efficacy.
Important skills for a CRA include strong communication and organizational abilities, keen attention to detail, knowledge of clinical practices, and analytical skills. CRAs also need to be proficient in using specialized software for data analysis and trial management. Certifications such as Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP) are typically required. Prior to becoming a CRA, individuals might have roles such as Clinical Research Coordinator, Clinical Trial Assistant, or Research Nurse, gaining necessary experience in managing clinical trials and working in a research setting.
Work includes participant recruitment, enrollment, study visits and data collection in accordance with the protocol and good clinical practice guidelines....
Clinical Research Specialist University of Minnesota Twin Cities
- Minneapolis, MN
- 3 days ago
- Minneapolis, MN
- 3 days ago
Work includes participant recruitment, enrollment, study visits and data collection in accordance with the protocol and good clinical practice guidelines....
Associate Clinical Research Coordinator - Comprehensive Cancer Center
- Rochester, MN
- 5 days ago
- Rochester, MN
- 5 days ago
.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status...
ESSENTIAL JOB FUNCTIONS We are recruiting for a Senior Clinical Research Associate to join our team....
ESSENTIAL JOB FUNCTIONS We are recruiting for a Senior Clinical Research Associate to join our team....
Principal Clinical Research Specialist - Neuromodulation
- Minneapolis, MN
- 11 days ago
- Minneapolis, MN
- 11 days ago
Oversees and resolves operational aspects of clinical trials in conjunction with project teams following standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations...
Oversees and manages operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country...
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
Ameriprise Financial Director, Bank CRA Officer in Minneapolis , Minnesota In this role, you will be responsible and accountable for all aspects of the Community Reinvestment Act (CRA) program for...
Thorough understanding of Good Clinical Practice (GCP)....
Clinical Research Associate will ensure that clinical centers perform the clinical study according to the study protocol and regulatory standards by qualifying, training, monitoring and overseeing study...
Demographic Data for Minnesota
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Minnesota
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Minnesota offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Federal Housing Administration
- Consumer Lending
- Mortgage Lending
- FHLMC
- Federal National Morgage Association
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Institutional Review Board
- ICH GCP
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Cancer Research
- Drug Development
- Scientific Research
- Site Management
- Pharmacovigilance
- Biotechnology
- Clinical Trials
- Neuroscience
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Affirmative Action
- Collections
- High School Diploma
- Investigation
- Written Communication
- Auditing
- Documentation
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Teamwork
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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