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Team Leadership
Primary Responsibilities:
- Provide high-level logistical support for clinical study operations, including study start-up, supplies, site qualification, and monitoring.
- Develop study-related documents with minimal guidance and manage contracting, budgets, and vendor payments.
- Support data management, oversee clinical trial supplies, and train CROs and site staff on study requirements.
Qualifications:
- BA/BS in life sciences or related field, or equivalent.
- Minimum 4 years of experience on clinical studies in academic, biopharma, diagnostics, or medical device fields.
Knowledge, Skills and Abilities:
- Experience with EDC systems and familiarity with Trial Master File organization.
- Competency in SOPs, ICH-GCP, and FDA Regulations.
- Strong analytical, interpersonal, and communication skills.
What We Offer:
- Competitive benefits including medical, dental, vision, life, and disability plans.
- Fertility care benefits, pregnancy and baby bonding leave, and 401k.
- Commuter benefits and a generous employee referral program.
Natera
Natera is a global leader in cell-free DNA testing dedicated to oncology, women’s health, and organ health. Our team consists of highly dedicated professionals from world-class institutions who care deeply for our work and each other, working hard and growing quickly.