Executive - Clinical Research
Executive - Clinical Research
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Objective
Provide administrative support in management of clinical research.
Principal Accountabilities :
Principal Accountabilities
(A) Operational
Coordinate with the principal investigators finance/legal department and respond to the feasibility questionnaire for conducting clinical research/trials.
Liaison with the Pharmaceutical company/CRO for costing/budgeting and finalizing clinical trial agreement.
Provide secretarial support to ethical committee by arranging meetings managing ethical committee notifications and implementing decisions.
Project management for the trials in compliance with GCP (Good Clinical Practice).
Supervise the coordinators for each trial.
Ensure ethical patient enrollment and meticulous documentation.
Liaison with CRO / Pharma Company for external audits.
Update ethic committee interim review report of trials.
Ensure data (case report form) validation.
Raise invoice to CRO / Pharma Company as per project milestone.
Maintain project notebook (including correspondence records).
Maintain client contact under the direction of the Director Technical analysis according to schedule or as deemed necessary.
Provide final quality assurance check of research report.
Update knowledge in statistical concepts methods and techniques and maintain state of the art statistical applications in clinical research.
Develop project analysis plan including computer-generated table specifications statistical analysis plan and research report format
Performance Parameters
Efforts to enhance clinical outcomes of their concerned specialty.
Participation in Clinical Research Activities.
Quality and timeliness of the service delivery of the patients & error free Medical care in the specialty.
Implementation of Post Discharge programme.
Medical Records keeping with in the specialty.
Participation in quality audits & preventive & corrective actions.
Participation in the CME programmes & initiatives in skill enhancement of reporting subordinates.
Implementation of infection control & waste management in their concerned areas.
Strategic inputs in Clinical committees & consultants meeting.
Education
Graduate
Experience
4 years in Clinical Research in a good institute / Pharma company.
Knowledge
Energetic and self Motivated
Strong interpersonal persuasion and facilitation skills with people of different levels background and personality styles.
Good computer skills. Preferably having some knowledge of Biostats as well.
Employment Type
Full Time
