
Clinical Research Associate
CenExel
full-time
Posted on:
Location Type: Remote
Location: United States
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Tech Stack
About the role
- Monitors clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Conducts site selection, initiation, monitoring, and close-out visits.
- Reviews case report forms (CRFs) for accuracy and completeness.
- Verifies source documents to ensure data integrity.
- Liaises between sponsors and clinical trial sites to resolve issues.
- Ensures timely reporting and resolution of adverse events.
- Maintains and updates study documentation and records.
- Trains site staff on study protocols and compliance procedures.
- Ensures proper handling and storage of investigational products.
- Prepares monitoring visit reports and presents findings.
Requirements
- Must be able to effectively communicate verbally and in writing.
- Bachelor’s degree in life sciences, health sciences, nursing, or a related field.
- 1–3 years of experience in clinical research.
- Certification from recognized organizations (e.g., SOCRA, ACRP) is a plus.
- Strong understanding of clinical trial processes, GCP, and regulatory guidelines.
- Excellent attention to detail and organizational skills.
- Proficiency with clinical trial management systems (CTMS) and Microsoft Office Suite.
- Strong communication and interpersonal skills.
Benefits
- Health Insurance
- Dental
- Vision
- LTD
- STD
- Life Ins
- 401k
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringcase report form (CRF) reviewdata integrity verificationadverse event reportingstudy documentation maintenancesite staff traininginvestigational product handlingmonitoring visit report preparationclinical research experienceGood Clinical Practice (GCP)
Soft Skills
effective communicationattention to detailorganizational skillsinterpersonal skills
Certifications
SOCRA certificationACRP certification