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Study Assistant

Frontage Laboratories
Posted 22 days ago, valid for 12 days
Location

Painesville, OH, US

Salary

Competitive

Contract type

Full Time

Health Insurance
Life Insurance
Disability Insurance

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Sonic Summary

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  • The Study Assistant position at Frontage Laboratories Inc. in Concord, OH, is an on-site role reporting to the Study Support Team Leader.
  • Candidates should possess an Associate’s or Bachelor’s Degree in Life Sciences, communication, English, or a related discipline, with a willingness to train individuals with relevant backgrounds.
  • The role requires proven teamwork abilities, excellent communication skills, and basic computer knowledge, with experience in Provantis or similar LIMS software considered a plus.
  • The position involves generating data tables, drafting reports and protocols, and reviewing study data while ensuring compliance with SOP and regulatory guidelines.
  • The salary for this role is competitive, and the company offers a generous benefits package including health insurance and a 401(k) plan.
 

Title: Study Assistant 

Location: Concord, OH (on-site)

Reports To: Study Support Team Leader

Company

Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary:

We are seeking a highly-motivated, detail-oriented team member to support client-driven projects. The successful candidate will be an active member of the Study Support Group and will assist Study Directors on assigned studies with general client needs, drafting and issuing protocols/protocol amendments, preparing subreports, running Provantis data tables, and reviewing study data all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines.


Roles and Responsibilities:

  • Generate Provantis data tables and create PDFs of tables for reporting
  • Draft subreports (Ophthalmology, Anatomic Pathology, Clinical Pathology, ECG), protocols, and protocol amendments.
  • Review study data, data binders, and documents generated by Study Directors/Study Support as needed.
  • Assist with drafting deviations as they arise
  • Update Toxicology Project Management system as milestone tasks are completed.
  • Review and edit grammar, styles, typefaces, and formatting based on report writing style guidelines for all generated documents.
  • Reviewing Locomotor Activity Data spreadsheets and ECGs.
  • Data entry into Provantis for various studies


Education and Requirements:

  • Associate’s or Bachelor’s Degree preferably in Life Sciences, communication, English, or similar related discipline. 
    • An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education.
    • Willing to train individuals with correlating background, education, or skills.
  • Proven ability to successfully work in a team environment.
  • Excellent oral and written communication skills.
  • Basic computer knowledge (e.g. Microsoft Word, Excel, Adobe Acrobat)
    • Experience with Provantis or similar LIMS software is a plus.


Salary and Benefits:

Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc.


Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.


 

 




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