CCT Research is growing! We’re looking for a great Study Architect Specialist to join us in our Mission: Leading today's trials, offering tomorrow's hope. And help make progress toward our Vision: For future generations to live in a world free of disease.    

Ideal Candidate:  

You are self-driven with a "can-do" attitude, team-building skills, adapt quickly and thrive independently, effectively communicate across multiple departments, and be thorough with details. ‍The ideal primary skills include logical thinking, ability to prioritize, multi-tasking on competing deliverables, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

You’ll play a key role in assisting in the support of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. You’ll work closely with study team members under the direct supervision of the Manager of Patient Utilization to prepare and maintain electronic source documents for clinical research studies, and to build the studies in CCT’s Clinical Trial Management System (CTMS).  

Key Responsibilities for Study Architect Specialist:

• Utilize the protocol, case report files (CRFs), budget and other resources to create source documents and study builds digitally in the CTMS by due date

• Develop strong working relationships and maintain effective communication with study team members
• Collaborate with various departments to ensure accuracy and functionality of final products  
• Comply with CCT, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines
• Complete all assigned training required for the position
• May perform other duties not specifically listed in this job description as assigned by their immediate supervisor  

Desired Knowledge Skills and Abilities:

• Experience reading and understanding technical literature
• Familiarity with medical terminology  

Required Knowledge Skills and Abilities:

• Knowledge and ability to apply Good Clinical Practice (GCP)/ International Council for Harmonization (ICH) and applicable regulatory guidelines

• Exceptional organizational skills, a keen attention to detail and follow-through
• Comfortable with computers and web-based databases, Sharepoint
• Effective communication skills
• Demonstrated proficiency in use of Microsoft Word, Excel and PowerPoint
• Able to effectively prioritize tasks and shift priorities quickly when needed