Clinical Program Manager - Clinical Operations Study Management

March 16

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Eikon Therapeutics

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Pioneering a new method of drug discovery based on tracking and measuring movement of individual proteins in live cells

201 - 500

Description

• Team leader and builder, managing trial deliverables and timelines • Works with minimal oversight from Clinical Operations Senior Director or Director • Ensure clinical studies are conducted in accordance with regulations and guidelines • Manage ancillary vendor relationships • Provide regular updates on study progress to stakeholders • Oversee and be in compliance with Eikon processes • Expected to lead, manage, hire global regional Clinical Operations Study Management personnel • Contribute to initiatives and projects adding value to Eikon Therapeutics

Requirements

• Bachelor's or advanced degree in a relevant scientific or healthcare field • At least 5 years of experience in effectively running global clinical studies in oncology or neuroscience • In-depth knowledge of ICH-GCP, EMEA guidelines, and other relevant regulations and guidelines • Proven ability to manage clinical studies within timelines and budgets while maintaining high quality standards and patient safety • Strong leadership and communication skills • Experience with management of budget, resources, headcount, processes, and controls • High sense of accountability and urgency • Growth mindset and capable of working independently • Ability to work onsite at least 3 days a week

Benefits

• 401k plan with company matching • Medical, dental, and vision insurance covered by Eikon • Mental health and wellness benefits • Weeklong summer and winter holiday shutdowns • Generous paid time off and holiday policies • Life/AD&D Insurance covered by Eikon • Enhanced parental leave benefit • Daily subsidized lunch program when on-site