Job Description

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

Job Tags

Contract work, Immediate start,

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