Clinical Trial Associate

Roles & Responsibilities:
• Assist Project Manager and Clinical Research Associates (CRAs) in updating and maintaining clinical systems to track site compliance and performance within project timelines
• Help the clinical team in preparing, handling, distributing, filing, and archiving clinical documentation and reports according to SOPs
• Assist with periodic review of study files for accuracy and completeness
• Track and manage Case Report Forms (CRFs), queries, and clinical data flow
• Process Data Collection Forms including login, tracking, and quality control as appropriate for the study
• Assist in preparing Quality Management System documentation and support audit preparations
• Provide general administrative support to the Clinical Operations Department
• Support Clinical teams in completing all required tasks to meet departmental and project goals
• Set up, organize, and maintain clinical study documentation (e.g., Main Study Files, CRFs) including preparation for audits, reconciliation, and archival
• Assist in coordinating Investigator payments, if applicable
• Support preparation of slides, overheads, and presentations for projects, departmental meetings, sponsors, and business development

Qualification:
• Bachelor of Pharmacy, Master of Pharmacy
• Degree or equivalent experience in a Clinical Background (Life Sciences, Pharmacy, Clinical Research, etc.)

Experience:
• 2–3 years of professional experience in clinical research or medical device trials

Skills:
• Strong understanding of medical device regulations
• Excellent written and verbal communication skills
• Familiarity with clinical systems and documentation standards

About the Organization:
Concept Medical is a globally recognized medical device company specializing in innovative interventional technologies, playing a key role in advancing cardiovascular and endovascular treatment solutions.