Data Entry / Memphis TN 38134

Mindlance

Memphis (TN)

On-site

USD 40,000 - 50,000

Full time

14 days+

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Job summary

A national recruiting firm is seeking a Business Data Entry professional to support the Safety Department in Memphis. Responsibilities include accurate data entry, supporting project managers, and ensuring document organization. The ideal candidate is fluent in English, with a preference for scientific knowledge and clinical research experience. This is a temporary 3-month contract position offering a unique opportunity to contribute to the Safety team. Interested applicants are encouraged to submit their chronological resume.

Qualifications

  • Fluency in English; additional languages a plus.
  • Scientific knowledge preferred but not mandatory.
  • Clinical Research experience preferred but not mandatory.

Responsibilities

  • Enter data into safety database with accuracy.
  • Interact with Safety Managers/Safety Scientists on projects.
  • Perform quality control on entered cases.

Skills

Fluent in English
Scientific knowledge
Clinical Research experience

Job description

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.

Job Description

Business Data Entry

Location 1620 Century Center Parkway, Memphis TN 38134

Division Pharma

Contract 3 Months

Qualifications

For Clinical Safety Data Associate Roles:

Input information from a variety of sources into a computer database. May take customer orders and enter them into a pre-established tracking system. Verify recorded information to ensure accuracy and completeness of data. Identify and correct errors. Update files and records. Assemble, batch, and distribute data.

  • Imaging and indexing of paper DCT’s received via mail
  • Answer questions on DCT entry process and the query resolution process on an ongoing basis

Brief Description:

  • Performs data entry functions and other data functions for the Safety Department

Requirements:

  • Fluent in English; additional languages a plus, but not required
  • Scientific knowledge preferred, but not mandatory
  • Clinical Research experience preferred, but not mandatory

Specific Job Duties:

  • Support the Safety Managers/Safety Scientists
  • Interact with the Safety Managers/Safety Scientists to discuss ongoing projects
  • Be aware of and maintain the workflow and timelines for each project
  • Enter data into safety database with accuracy
  • Ensure filing of all documents and organize all filing systems
  • Interact with staff, clients or partners to ensure case information is adequate and accurate
  • Perform quality control on entered cases to ensure cases meet highest standards
  • Participate in and contribute to team meetings
  • Other duties assigned by management
  • Maintain accurate and complete documentation and system records of all inquiries to continuously improve the customer service experience and mitigate potential legal issues. Report to the proper group any allergy, adverse events, or duplicate therapy warnings that appear
  • Accurately enter eligibility paperwork, prescriptions, refills, and/or other information into system. Maintain accurate and complete documentation of all applications, mailers, orders, enrollment forms and new patients. Process order rejections and follow-up activities.
  • Efficiently perform specialized functions for each program with a high level of accuracy
  • Enter and interpret program materials to determine enrollment criteria; explain to the caller or other employees the necessary requirements to be on the program.

If you are available and interested then please reply me with your “Chronological Resume” and call me on (678)-405-3590 .

Additional Information

Thanks & Regards,

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