Clinical Research Assistant - QC Data Specialist
: Job Details :

Opportunity to join the Quality Department of one of the fast-growing clinical research companies!

This is an excellent opportunity for clinical research professionals to get into data and quality!

Ideal backgrounds would include experience working in healthcare quality, regulatory, or patient data. Clinical research experience is not required but is nice to have. If you are a Clinical Research Assistant or Coordinator looking to get into Data and Quality, please consider applying as well.

HIGHLIGHTS

• Play a major role in helping patients get involved in cutting-edge clinical trials - a meaningful healthcare position!
• Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays)
• Gain experience in the fast-growing world of clinical research and develop skills that are in high demand
• Monday - Friday 8:30 am - 5 pm
• The company is invested in growth, providing employees with unique opportunities for career advancement

POSITION

The Quality Control Data Management Specialist entails quality control and precise data entry for clinical studies, under the supervision of the Operations Manager. Key duties include reviewing study charts according to standards and protocols, accurately entering data into electronic systems, identifying discrepancies, and reporting issues. Additionally, the role involves collaboration with clinical research teams and sponsor representatives, attending meetings, assisting in sponsor visits, and supporting training procedures, with a focus on professionalism and efficiency.

COMPANY

Our client is a Clinical Research site network with over 25 research sites across the United States. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. They are a fast-growing site network with plans to grow from 17 sites to over 30 sites in 2024 alone.

QUALIFICATIONS

• Bachelor's degree or commensurate experience
• 1-3 years of experience within the field of clinical or biological research
• Experience working in healthcare quality, regulatory, and/or patient data
• Familiarity with Clinical Trial Management Systems (CTMS)
• Strong attention to detail, analytical skills, and precision