ALLEN SPOLDEN
51 - 200 employees
🏥 Healthcare
đź’Ľ Consulting
🏠Manufacturing
Healthcare • Consulting • Manufacturing
ALLEN SPOLDEN is a workforce solutions provider specializing in talent and research solutions for the pharmaceutical, biotech, healthcare, and public health sectors. They offer services including functional service provider (FSP) solutions, data management, regulatory affairs guidance, and tailored staffing services to meet the specific needs of clinical research projects. Their expertise is aimed at driving efficiency, enhancing productivity, and ensuring compliance throughout clinical trial operations.
Clinical Trial Associate
Job not on LinkedIn
đź•’ July 21
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ALLEN SPOLDEN
51 - 200 employees
🏥 Healthcare
đź’Ľ Consulting
🏠Manufacturing
Healthcare • Consulting • Manufacturing
ALLEN SPOLDEN is a workforce solutions provider specializing in talent and research solutions for the pharmaceutical, biotech, healthcare, and public health sectors. They offer services including functional service provider (FSP) solutions, data management, regulatory affairs guidance, and tailored staffing services to meet the specific needs of clinical research projects. Their expertise is aimed at driving efficiency, enhancing productivity, and ensuring compliance throughout clinical trial operations.
đź“‹ Description
• Support the day-to-day coordination of clinical trials • Maintain and organize Trial Master File (TMF) documentation • Assist with regulatory document collection and tracking • Coordinate communication with clinical sites, sponsors, and vendors • Track study milestones, deliverables, and timelines • Review study documentation for completeness and accuracy • Support investigator meetings and study start-up activities • Assist with data management and query resolution • Ensure compliance with Good Clinical Practice (ICH-GCP), company SOPs, and regulatory requirements • Prepare reports and maintain accurate study records
🎯 Requirements
• Associate's or Bachelor's degree in a relevant field, including Psychology, Life Sciences, Biology, Biomedical Science, Public Health, Health Sciences, Nursing, Healthcare Administration, Medical Laboratory Science, or related scientific or healthcare disciplines • Clinical research experience preferred • Strong organizational and time management skills • Excellent written and verbal communication skills • High attention to detail • Proficiency with Microsoft Office, including Excel, Word, Outlook, and PowerPoint • Ability to manage multiple priorities in a fast-paced environment • Working knowledge of ICH-GCP guidelines and clinical research processes preferred
🏖️ Benefits
• Competitive hourly compensation • Flexible contract assignment • Opportunity to gain experience supporting clinical trials • Potential for contract extension based on business needs and performance
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