Title:Clinical Data Coordinator 
Location: Brentwood, TN (ONSITE ROLE) 
Type: 8 month Contract
Schedule: Core business hours M-F
Start Date: ASAP

Responsibilities:
Duties include but are not limited to:
• Support data entry activities to meet study data needs and deadlines
• Data abstraction from diverse sources
• Obtain source documentation for patients enrolled into clinical trials and data registry
• Maintain Data Registry as directed
• Assist with Data validation, conflict resolution and quality assurance
• Supports Clinical Project Manager to meet industry trial data deadlines
• Obtain source documentation for patients enrolled into clinical trial
• Assist Clinical Project Manager with case report form completion
• Assist Clinical Project Manager with query resolution
• Assist in SAE reporting and tracking
• Create and maintain patient visit tracking spreadsheets
• Maintain and archive study documents
• Meet with clinical study sponsor representatives as requested
• Develop and maintain file management and collaboration systems
• Maintain calendar
• Initiate improvements, tools, processes, and forms to enhance the efficiency and quality of work
• Attend meetings as assigned and report on actions
• Participate in educational activities and programs
• Maintain strictest confidentiality
• Work closely and effectively with all other department colleagues
• Assist other staff as requested and performing other related work as needed.
• Throughout the conduct of the clinical trial assesses adherence to Company SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines
• All other duties as assigned

Requirements: 
• High School Diploma Required
• Bachelor’s Degree Preferred
• 1+ years of experience in healthcare, research, or other science related field
• Knowledge of scientific, medical, and regulatory terms
• Must have an understanding of clinical research process
• Knowledge of GCP and GMP
• Professional writing and communicating skills required
• Organizational and prioritization skills required
• Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel
• High computer literacy and ability to learn new software if required
• Ability to work both collaboratively and independently
• Interpersonal skills, detail oriented, and meticulous
• Ability to multi-task in fast paced environment is essential.
• Ability to manage, organizes, and makes decisions

Ref: #568-Clinical

System One, and its subsidiaries including Joulé, ALTA IT Services, TeamPeople, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.