Entry-Level Cosmetic Clinical Study Coordinator

Apex Systems

Phoenix (AZ)

On-site

USD 62,000 - 68,000

Full time

4 days ago
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Benefits offered by this job

401K
HSA
Employee Assistance Program (EAP)
Stock purchase program

Job summary

Apex Systems is seeking 3 Clinical Study Coordinators to join our science-driven team in a Monday–Friday daytime schedule (8:00 am–5:00 pm). Some studies may require up to 12-hour shifts with modified days.

The role focuses on planning and managing cosmetic and personal care product studies, including safety and efficacy assessments. The candidate will engage in hands-on study setup, participant consenting, data collection, and administrative support, contributing to a fast-paced, collaborative

Qualifications

  • Great interpersonal skills and strong organizational skills are a must.
  • BS in a scientific field required; no industry experience needed beyond applying scientific principles and providing excellent customer service.

Responsibilities

  • Set up studies and get all needed materials and documents in order before participants arrive.
  • Consenting participants on the test procedures and potential adverse reactions to products.
  • Follow study procedures by measuring products, applying to test participant, ask participant questions on their experience, make observations on any skin reactions, and evaluate the positive benefits of the product.
  • Document all observations and physical evaluations/measurements, and collect data for final reports.
  • Provide administrative support (word processing, Excel data management) as needed to Study Administrator.

Skills

Interpersonal skills
Organizational skills
Customer service

Education

BS in a scientific field

Job description

Apex Systems is seeking 3 Clinical Study Coordinators to join our science-driven team in a Monday–Friday daytime schedule (8:00 am–5:00 pm). Some studies may require up to 12-hour shifts with modified days.

The role focuses on planning and managing cosmetic and personal care product studies, including safety and efficacy assessments. The candidate will engage in hands-on study setup, participant consenting, data collection, and administrative support, contributing to a fast-paced, collaborative

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