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POSITION SUMMARY:
- Responsible for the overall operational execution of clinical studies on one or more clinical projects/programs; from study concept through study completion
- Ensure that trial timelines, costs, and quality metrics are met, and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements
- Design and execute clinical research activities
QUALIFICATIONS:
- BA/BS degree in life sciences, related field, or equivalent
- Minimum of 4 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields
KNOWLEDGE, SKILLS AND ABILITIES:
- Experience with clinical EDC systems
- Familiarity with the organization and structure of the Trial Master File (TMF)
- Familiarity with bio sample management, sample processing, and biobanking best practices
Natera
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.