3,00,000 - 6,50,000 P.A
Dear Candidate,
Opening in Quintiles for Records Management Professionals.
Exp: 3 years - 6 years
Criteria: Candidates having experience in Clinical Records Management, CRC, Clinical Research Co- ordinators,Clinical Data Mining, Clinical Data Documentation, Clinical Data Validation can apply for this role.
Designation: Sr. Clinical Process Associate / Clinical Process Specialist
Job - Description
Purpose
Apply clinical research expertise to provide project related assistance across complex and multiple project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
RESPONSIBILITIES
Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and maintain effective project/ site communications
Create and maintain relevant project documents// trackers Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information Review, evaluate and recommend modifications to designated processes Oversee and participate in document management (creation, review, maintenance, storage, as applicable)
Participate in (study) team meetings and implement action items
Collaborate with the project lead/team members in creation/review of study documents
Act as point of contact for assigned deliverables for specific customers or projects
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Escalate quality issues to relevant stakeholders and/or line manager.
If interested please forward your CV to thenmozhi.r@quintiles.com
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