07 Apr

Clinical Research Coordinator - Ahmedabad - Ethos Management Projects

Position
Clinical Research Coordinator
Company
Ethos Management Projects
Location
Ahmedabad GJ
Opening
07 Apr, 2017 30+ days ago

Ethos Management Projects as the company that open the jobs vacancy, have some qualification and spesification especially for the Clinical Research Coordinator jobs vacancy. To find out more information and about qualification and spesification details, walkin interview schedule, the address of the company, the company contact info (email/phone number) of Ethos Management Projects company, please start to apply for the job vacancy with fill the jobs application with click the 'Apply This Job' button below.

Job Responsibility of Clinical Research Coordinator–
• Preparing and submitting regulatory documents to EC and Sponsor
• Preparing and submitting site SOPs to EC and sponsor
• Attending investigator meeting
• Developing a preliminary budget and verify all costs incurred
• Helping PI negotiate the study budget direct costs with sponsor to cover all costs
• Preparing and handling site selection visit
• Preparing for study initiation
• Recruiting study participants in the study
• Screening and scheduling of study participants
• Getting voluntary informed consent from study participants
• Counseling study participants about study protocol expectations for them
• Performing study/protocol procedures in a detailed, accurate manner
• Maintaining all the study related files
• Tracking and maintaining the study budget and payments, including invoicing the sponsor for completed work
• Tracking study participants, avoiding lost-to-follow-up
• Documenting and submitting an adverse event
• Processing and shipping laboratory samples
• Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel
• Completing case report forms for PI review and approval
• Maintaining study-specific supplies
• Preparing for study closure and archiving

Key Skills:
Job Responsibility of Clinical Research Coordinator–
• Preparing and submitting regulatory documents to EC and Sponsor
• Preparing and submitting site SOPs to EC and sponsor
• Attending investigator meeting
• Developing a preliminary budget and verify all costs incurred
• Helping PI negotiate the study budget direct costs with sponsor to cover all costs
• Preparing and handling site selection visit
• Preparing for study initiation
• Recruiting study participants in the study
• Screening and scheduling of study participants
• Getting voluntary informed consent from study participants
• Counseling study participants about study protocol expectations for them
• Performing study/protocol procedures in a detailed, accurate manner
• Maintaining all the study related files
• Tracking and maintaining the study budget and payments, including invoicing the sponsor for completed work
• Tracking study participants, avoiding lost-to-follow-up
• Documenting and submitting an adverse event
• Processing and shipping laboratory samples
• Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel
• Completing case report forms for PI review and approval
• Maintaining study-specific supplies
• Preparing for study closure and archiving


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