CenExel
1001 - 5000 employees
Founded 2018
💊 Pharmaceuticals
🔬 Science
🤝 B2B
Pharmaceuticals • Science • B2B
CenExel is a U. S. -based clinical research site network operating multiple Centers of Excellence nationwide that run and support clinical trials to advance new therapies. The company partners with life science and pharmaceutical sponsors to manage participant recruitment, trial operations, and data collection, emphasizing patient experience, quality, and scientific rigor. CenExel also offers a mobile app to connect patients with trials and participates in multisite research collaborations to accelerate drug development.
Clinical Research Associate
Job not on LinkedIn
🕒 March 26
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CenExel
1001 - 5000 employees
Founded 2018
💊 Pharmaceuticals
🔬 Science
🤝 B2B
Pharmaceuticals • Science • B2B
CenExel is a U. S. -based clinical research site network operating multiple Centers of Excellence nationwide that run and support clinical trials to advance new therapies. The company partners with life science and pharmaceutical sponsors to manage participant recruitment, trial operations, and data collection, emphasizing patient experience, quality, and scientific rigor. CenExel also offers a mobile app to connect patients with trials and participates in multisite research collaborations to accelerate drug development.
📋 Description
• 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 • Assumes other duties and responsibilities as assigned
🎯 Requirements
• 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
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