Scientific Support

October 8, 2026
$22 / hour
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Job Description

Job Summary:

  • Responsible for reviewing all study data to ensure it is complete and GLP compliant.
  • Ensure that all data received for review follows SOP and regulatory guidelines that apply to the recording of study data.
  • Interact with Scientist, QA staff and other departments with regards to data.

Duties & Responsibilities:

  • Complete data review on all paper and electronic data produced in operational departments.
  • Ensure all forms that require data review and electronic data are in compliance with Standard Operating Procedures (SOPs) and forms are updated as needed.
  • Ensure all data corrections are completed by the appropriate staff members and that they are completed correctly.
  • Communicate with department management and Scientist regarding any issues related to data collection that impact the recording of data.
  • Assist in departmental training by providing assistance with training on correct methods of data notation and correction as it relates to study data review.
  • Assist in revising and developing department forms.
  • Archive, collate, and organize all completed and reviewed data and/or file as appropriate.
  • Collaborate with QA staff to ensure GLPs are being followed for the recording of data.
  • Assist with department filing as needed.
  • Perform all other related duties as assigned.

Required Skills & Education:

  • High school diploma or General Education Degree (G.E.D.) required.
  • Associates Degree preferred.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Strong organizational, communication and listening skills with acute attention to detail.
  • Basic understanding of processes used for study data collection.
  • Basic understanding of SOPs, FDA GLPs and GCP and other applicable regulatory guidelines governing the recording and review of study data.
  • Basic understanding of algebraic math and scientific concepts.
  • Ability to work effectively as a member of a team.
  • Experienced computer skills; familiarity with Microsoft Office software and specifically with Word and Excel.
  • Ability to work effectively under minimum direction.

Physical Demands:

  • Regularly operates a computer and occasionally operates other office productivity machinery such as a label maker, copy machine, and computer printer.
  • Regularly communicates with employees.
  • Regularly provides information to and receives information from/through various technologies, media, sources and contacts.
  • Must be able to exchange accurate information in these situations.
  • Specific vision abilities required by this job include close vision and the ability to adjust focus.
  • Regularly moves about inside the office to access file cabinets, office machinery, etc.

Work Environment:

  • General office and laboratory working conditions, the noise level in the work environment is usually quiet.
  • Record observations and measurements and report results for basic to moderately complex lab/research tasks.
  • Coordinate shipment and receipt of equipment to vendors.
  • Review data recorded by others for quality control.
  • Assist technical personnel with clerical duties (e.g., filing, making copies, etc.).
  • Assist in the collection and disposal of potentially hazardous material.
  • Assist with ordering, receipt and distribution of ordered consumables / lab reagents and complete chain of custody.
  • Install and operate basic to moderately complex lab equipment and perform routine maintenance as needed.
  • May perform limited troubleshooting of instruments as appropriate for assigned area.
  • Monitor inventory and stock assigned areas.
  • May prepare materials and data for routine shipment or archival.
  • May be responsible for preparing simple lab solutions (e.g., buffers, media/common vehicles, cleaning solutions).
  • May generate reports, data, and forms.
  • Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
  • Perform all other related duties as assigned.