Clinical Research Associate Jobs in Cincinnati, OH
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.
Bilingual Clinical Research Associate (CRA) - Montreal
- Medpace, Inc.
- Cincinnati, OH
- 60+ days ago
- Cincinnati, OH
- 60+ days ago
Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada....
In PersonExperienced Clinical Research Associate (remote-based)
- Medpace
- Cincinnati, OH
- 60+ days ago
- Cincinnati, OH
- 60+ days ago
Job Summary Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical Operations team in Austria (home-based)....
RemoteClinical Trial Associate- Trial Master File (TMF)
- Medpace, Inc.
- Cincinnati, OH
- 60+ days ago
- Cincinnati, OH
- 60+ days ago
We are currently hiring individuals seeking an exciting career in clinical research, managing our Trial Master File....
In PersonClinical Research Associate - Cincinnati, OH (Entry-Level)
- Medpace, Inc.
- Cincinnati, OH
- 90+ days ago
- Cincinnati, OH
- 90+ days ago
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields....
RemoteClinical Research Associate (PhD Candidates)
- Medpace, Inc.
- Cincinnati, OH
- 90+ days ago
- Cincinnati, OH
- 90+ days ago
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives...
RemoteClinical Research Associate - Clinical Research Coordinator Experience
- Medpace, Inc.
- Cincinnati, OH
- 90+ days ago
- Cincinnati, OH
- 90+ days ago
This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace...
RemoteHome-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity
- Medpace, Inc.
- Cincinnati, OH
- 90+ days ago
- Cincinnati, OH
- 90+ days ago
Experienced Clinical Research Associate (CRA) - join our growing team! Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team....
RemoteDemographic Data for Cincinnati, OH
Moving to Cincinnati, OH? Find some basic demographic data about Cincinnati, OH below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Cincinnati, OH
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Cincinnati, OH offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Fannie Mae
- Good Clinical Practice
- ICH Guidelines
- Study Management
- Sample Preparation
- Institutional Review Board
- Clinical Monitoring
- ICH GCP
- Clinical Trial Management System
- Drug Development
- Biostatistics
- Gene Therapy
- Pharmacovigilance
- Cancer Research
- Biology
- Site Management
- Clinical Trials
- Clinical Operations
- Clinical Research
- Biotechnology
- Neuroscience
- Medical Device Sales
- FDA Regulations
- Oncology
- Data Collection
- Standard Operating Procedures
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Documentation
- Implementation
- Verbal Communication
- Reporting
- Policy Development
- Data Entry
- Collaboration
- Education Experience
- Microsoft PowerPoint
- Bachelor's Degree
- Microsoft Word
- Regulations
- Research Skills
- Microsoft Excel
- Microsoft Office
- Problem Solving
- Staff Supervision
- Scheduling
- Computer Skills
- Time Management
- Leadership
- Communication Skills
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