Clinical Research Associate

NextCode Placement is presenting a Clinical Research Associate opportunity with an unspecified employer. The role monitors clinical trial sites, supports protocol and regulatory compliance, verifies study data, and works with site personnel and clinical operations teams to help ensure study quality and timely execution.

Responsibilities

• The CRA will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, and supporting adherence to applicable regulatory and ethical standards
• Key responsibilities include reviewing source documents and Case Report Forms (CRFs), verifying data accuracy and completeness, supporting site staff with clinical trial procedures, and documenting findings through monitoring reports
• The CRA will collaborate with clinical operations teams and support site initiation, routine monitoring, and closeout activities
• The role also involves identifying and helping resolve issues that may affect patient safety, protocol compliance, data integrity, or study timelines
• Regular communication with investigators, clinical research coordinators, site personnel, and internal stakeholders will be required to ensure study quality and timely execution

Preferred

• Master's degree or advanced qualification in Clinical Research, Life Sciences, Pharmacy, Biotechnology, or a related discipline is a plus
• Familiarity with clinical research documentation, EDC systems, or clinical trial processes is an advantage
• ACRP, SOCRA, or other relevant clinical research certifications are a plus
• Clinical Research
• Life Sciences
• Pharmacy
• Biotechnology
• Clinical Research Documentation
• EDC Systems
• ACRP Certification
• SOCRA Certification

Company

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

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, Biology, or a related field
• Hands-on experience as a Clinical Research Associate (CRA) or in a closely related clinical research position
• Strong understanding of clinical trial protocols, GCP, and applicable regulatory requirements
• Knowledge of clinical trial processes, including site monitoring, documentation, source data verification, and data review
• Experience with clinical operations, site management, and collaboration with cross-functional teams
• Familiarity with Electronic Data Capture (EDC) systems and clinical trial management tools
• Proficiency in Microsoft Office, particularly Excel and Word
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks and study activities
• Excellent written and verbal communication skills
• Ability to build and maintain professional relationships with investigators, coordinators, and site personnel
• Strong problem-solving and analytical skills
• A Master's degree in Clinical Research, Life Sciences, Pharmacy, Biotechnology, Biology, Public Health, or a related field
• Relevant clinical research internship, academic research, or clinical trial experience
• Understanding of GCP and clinical research fundamentals
• Strong documentation, communication, analytical, and organizational skills
• Master's degree or advanced qualification in Clinical Research, Life Sciences, Pharmacy, Biotechnology, or a related discipline is a plus
• Familiarity with clinical research documentation, EDC systems, or clinical trial processes is an advantage
• ACRP, SOCRA, or other relevant clinical research certifications are a plus

Required skills

• Clinical Research, Clinical Practice (GCP), Clinical Trial Protocols, Clinical Trial Site Monitoring, Source Data Verification, Clinical Operations, Site Management, Electronic Data Capture (EDC), Microsoft Excel, Microsoft Word, ACRP Certification, SOCRA Certification, Relationship Management

Preferred skills

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