- Under the supervision of a clinical project manager, perform clinical studies to support clinical innovation programs related to skin biology.
- Assist clinical team members in various aspects of clinical study, including e-monitoring of eCRF system, compiling study results and images, and QA/QC of study reports.
- Maintain and track all clinical team instruments and laptops. Ordering, shipping and labelling of study products to meet study timeline.
- Maintaining strong relationships with internal and external partners (CROs, global Advanced Research, Data Management Team, and Statistical Team), to ensure clinical study integrity.
- Serve as key Quality person in the team, to ensure compliance with global Quality guidelines and GDPR regulation.
- Bachelor degree in related field with 3-5 years of relevant working experience.
- Minimum of 1 year experience in managing and monitoring Human Clinical Trials in pharmaceutical, OTC, or personal care industries.
- Experience working with CROs; Solid understanding of good clinical practices and FDA guidelines;
- Working knowledge on methods of evaluation (instrumental and clinical) or diagnostic tools for evaluating product efficacy would be a plus.
- Good knowledge of Skin biology, and Dermatology.
- Strong communication, presentation and project management skills.
- Be able to work independently and to drive the projects forward with minimum supervision.
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Clinical Data Analyst I - Clark, United States - Cogent Infotech Corporation
Description
Advanced Research – Translational DiscoveryClinical Research Scientist (Contractor position)
Job Description: