Clinical Research Associate

NextCode Placement is recruiting for a Clinical Research Associate role in New York, NY; the hiring client is not identified. The role monitors clinical trial activities for protocol, regulatory, and ethical compliance and supports study start-up, conduct, and close-out.

Responsibilities

• The Clinical Research Associate will monitor clinical trial activities to ensure adherence to study protocols, regulatory requirements, and ethical standards
• Daily responsibilities include reviewing site documentation, verifying source data, tracking participant enrollment, and ensuring timely reporting of adverse events
• The role involves collaborating with clinical operations teams, investigators, and site staff to support study start-up, conduct, and close-out
• The Clinical Research Associate will also assist with training site personnel, maintaining accurate records, and contributing to continuous improvement of clinical research processes

Preferred

• advanced degree or certification in clinical research is an advantage
• Advanced Degree
• Clinical Research Certification

Company

• Tech recruitment and career placement services
• Sheridan, Wyoming, USA
• http://nextcodeplacement.com/
• Founded in 2020
• 51-200 employees

Qualifications

• Strong understanding of clinical trial protocol development and implementation, with the ability to interpret and apply protocol requirements
• Hands-on experience as a Clinical Research Associate, including site monitoring, documentation review, and compliance oversight
• Knowledge of clinical trials management and research methodologies, including data collection, analysis, and reporting practices
• Familiarity with clinical operations, including study start-up, site management, and trial logistics
• Bachelor's degree in life sciences, nursing, pharmacy, public health, or a related field
• Working knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements (e.g., FDA, EMA)
• Strong organizational and time-management abilities, with attention to detail and accuracy in documentation
• Effective written and verbal communication skills, including the ability to collaborate with cross-functional teams and site personnel
• Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC), and standard office software tools
• Advanced degree or certification in clinical research is an advantage

Required skills

• Clinical Operations, Clinical Practice (GCP), Clinical Trial Management Systems (CTMS), Clinical Trial Protocol Development, EMA Regulations, Electronic Data Capture (EDC), FDA Regulations, ICH Guidelines, Site Monitoring

Preferred skills

• AI Tools, Analyze How Well You Fit, Build Cover Letter, Company data provided by, Customize Your Resume, Growth Stage, Make your application stand out, Maximize your interview chances, Sheridan, Wyoming, USA, Tech recruitment and career placement services., Understand your strength & weakness, http://nextcodeplacement.com

Experience

• Mid level