JOB DETAILS
• Assist Project Manager with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
• Assist the PM in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures at Lambda.
• Ensure the TMF/E-TMF and Site master files are updated through out study as per study plan/applicable SOPs.
• Responsible for timely disbursal of Investigator payments based on Invoices received from sites
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Updates various study trackers assigned by Project Manager.
• Maintenance of trial related documents and files within the facility.
• Liaising with other functional groups and providing updates to Project Manager.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• Any other responsibilities as assigned by the Supervisor/HOD/Management.
KEY DELIVERABLES
ALLIED RESPONSIBILITIES
EXPERIENCE
At least 01 year experience in clinical research
EDUCATIONAL QUALIFICATION
B. pharm/ M.pharm/ MSc/ BAMS/BHMS having at least one year experience in clinical research
COMPETENCIES
Accountability
Communication
Work Ethic
Initiative
Leadership
Employment History
Technical Knowledge
Academic Qualifications
Motivation/Initiative
Interpersonal / Leadership skills
Presentation / Communication skills
Impression and Enthusiasm
Organizational Culture fit
Accomplishments & Strengths
Flexibility/Planning & Organizing