HYBRID IRVINE CA
Onsite 3 days a week – 2 days remote
Pay: $28-$30/hr
REQUIRED:
Bachelors Degree in a scientific field with one year clinical research experience
Some experience as a CRA and cosmetic skin care therapies
Supporting cosmetic consumer care skin line.
Must have some GCP knowledge and know what a monitoring visit is (can be obtained in an academic setting).
Must have some previous Excel experience.
Job Description:
Day to Day: supporting people and activities that surround clinical study monitoring
The Clinical Studies Specialist I (contingent) - Skincare (contingent role) will assist the Skincare Clinical Studies Specialist I and the Director II, Clinical Development and Global Scientific Affairs- Skincare with the operational execution and management of Skincare clinical research studies conducted with CROs and HCP research sites. The Clinical Studies Specialist I (contingent) will assist the Clinical Studies Specialist I with all clinical research activities from start-up to close out, data management and results presentations. The role is responsible for drafting study documents, organizing eTMF, CRF review, data entry, study photo transfer and presentation creation, and managing and summarizing data/results.
Responsibilities:
• Assists in the development and preparation of study protocols, informed consent documents, CRFs, subject instructions and all related study materials. Helps create and maintain the trial master file for each clinical study.
• Supports clinical study supply ordering and shipment as needed.
• Assists in performance tracking metrics for all activities needed for the execution of each assigned clinical study. Provides updates to the team as needed.
• Tracks receipt of completed study data, performs data entry and conducts statistical analysis, or assists in the management of a CRO to conduct the statistical analysis.
• Assists in the review of study data and supports generation of photo presentations, clinical study results presentations and summaries.
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