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.
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...
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...
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...
Thorough understanding of Good Clinical Practice (GCP)....
Basic understanding of biostatistics and trial design Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials, such as CFR 812, 50, 54, and ISO14155:2020...
Senior Clinical Research Specialist Pain Therapies (USA Remote)
- Fridley, MN
- 13 days ago
- Fridley, MN
- 13 days ago
Basic understanding of biostatistics and trial design Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials, such as CFR 812, 50, 54, and ISO14155:2020...
Clinical Research Associate- Minneapolis, MN/Dallas, TX, Miami/Tampa, FL/Charlotte, NC
- Minneapolis, MN
- 27 days ago
- Minneapolis, MN
- 27 days ago
Overview As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence....
At U.S. Bank, were on a journey to do our best. Helping the customers and businesses we serve to make better and smarter financial decisions and enabling the communities we support to grow and...
Chief Compliance & CRA Officer - Thrivent Bank In Formation
- Minneapolis, MN
- 45+ days ago
- Minneapolis, MN
- 45+ days ago
We exist to help people achieve financial clarity. At Thrivent, we believe money is a tool, not a goal. Driven by a higher purpose at our core, we are committed to providing financial advice,...
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...
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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
- Mortgage Lending
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- ICH GCP
- Institutional Review Board
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Cancer Research
- Drug Development
- Site Management
- Physiology
- Clinical Trials
- Biotechnology
- Neuroscience
- Clinical Operations
- Clinical Research
- Anatomy and Physiology
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Affirmative Action
- Collections
- Investigation
- Auditing
- Presentation
- Documentation
- Quality Assurance
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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