Labcorp Pharma Research Associate Vacancy – Apply Online
In addition to the tasks outlined in the Associate Document Coordinator position, learn to perform and manage activities related to technical data compilation and proofing and use of generic documents in compliance with appropriate protocol, Standard Operating Procedure (SOP), regulatory agency guideline, and client requirements in a timely, efficient, and quality manner. Take on DC-related team leader responsibilities, as appropriate (i.e. shipping calendar maintenance, process improvement projects, etc.). Mentor and/or train new DCs.
Job title: Report Associate, Metabolism (Early Development)
Location Bangalore, India
Job ID: 70942
Education/Qualifications:
- Bachelor of Science (BS) degree in science or related field a plus; experience may be substituted for education
- Ability to learn/utilize word processing software, database, spreadsheet, and specialized software
- Excellent communication and interpersonal skills
- Excellent attention to detail
- Ability to prioritize, organize, and manage time
Experience:
Years of experience in the job discipline: 2+ years in clinical research or pharma setting. Experience in pre-clinical preferred
To be considered for the Study Coordinator (SC) role, learn basic study document preparation/maintenance (i.e. prepare standard study protocols from outlines; prepare basic report shells for study directors/SCs to write in).
- Reads and understands study protocols, sample analysis outlines, amendments, regulatory requirements, and Covance SOPs/ as they pertain to basic data retrieval and the compilation from electronic systems (i.e. Tox Reporting, etc.).
- Gains familiarity and understanding in the use and preparation of generic document templates
- Gains familiarity and understanding in the use and preparation of client-specific requirements as they pertain to client document deliverables (protocols/reports)
- Works with Study Coordinators to assist in the preparation of study protocols and reports within client-specific requirements and/or the incorporation of contributing information into study reports.
- Learns to proof shipping paperwork prepared by others.
Takes on DC team leader responsibilities and acts as a mentor/trainer for new DCs, as appropriate/applicable - Learns and successfully performs reports to data QC of at least two study types.
- Other duties as assigned
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