Clinical Publishing Coordinator (Labcorp)

Roles and Responsibilities

Job Responsibilities

Follow applicable departmental Standard Operating Procedures, Work Instructions and departmental guidelines.

¨ Complete required trainings according to required timelines.

¨ Complete day-to-day tasks ensuring quality and productivity.

¨ Create and modify clinical investigator manuals, requisitions and other relevant materials according to SOW requirements to provide on-time, quality project related documentation.

Ensure that language translations of assigned project related documents are completed in a timely manner.

¨ Work effectively with peers to ensure delivery of appropriate DP documentation.

¨ Ensure timely escalation as needed.

¨ Other duties as assigned by management

Minimum Qualifications

Bachelor’s Degree in Science

Preferred Qualifications

6 months experience in clinical research and industry.

Master's Degree in Science

Additional Job Standards

·Perform in a general office setting.

· Sit for sustained periods of time in front of monitor.

· Perform with multiple interruptions.

· Requires the ability to manage multiple priorities.

· May be required to work overtime.

· Demonstrated ability to organize and communicate effectively.

· Demonstrated ability to pay attention to detail.

· Ability to work well with others.

·Ability to deliver consistent high quality of work.

·Ability to use computer and departmental tools.