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Mayo Clinic
Overview
The fellow will design and execute studies on cancer signaling and therapeutic resistance using proteomic and molecular profiling. Responsibilities include conducting in vivo validation and contributing to the preclinical evaluation of biologic agents.
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Compensation
$67,283 - $78,711 / YEAR
Posted
10 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
$70,000 - $95,000 / YEAR
The role is responsible for end-to-end safety case processing, including intake, triage, and regulatory submissions. It also involves maintaining the PV database, managing CAPAs, and ensuring global compliance and inspection readiness.
$85,000 - $115,000 / YEAR
12 days ago
The Office Administrator will oversee and streamline administrative and operational functions, ensuring smooth day-to-day business operations, including managing top-management meeting schedules and acting as the NJ Office Manager. Key duties involve managing the office budget, supplies, vendor identification, keycard access, and supporting new hire onboarding processes.
$60,000 - $80,000 / YEAR
3 months ago
