Data Entry Specialist

Description:

Enters clinical trials data into appropriate databases. Responsibilities include:

	Verifying data
	Following departmental and project guidelines for each assignment
	Performing assigned project tasks in accordance with project timelines
	Keeping manager informed about work progress and outstanding issues
	Utilizing appropriate codes for the tasks and projects
	Maintaining utilization level and quality control at all times

Requirements:

Requires a high school diploma or equivalent and at least one year of data entry experience, six months entering clinical data (medical terminology) preferred. Qualified candidates must be self-motivated, able to work independently, possess organizational and communication skills, be proficient with MS Office, be dependable, team oriented, and professional.

Needed in a growing, dynamic clinical research org. Work with a great team entering and verifying data for important clinical trials. Must have good utilization with accuracy, six months clinical experience (medical terminology) experience preferred. We're looking for good communication skills, dependability and team orientation.

To apply for one of the above positions, please submit your résumé or curriculum
vitae (CV) to careers@researchpoint.com

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