Manager, Study Start Up

Required

• You are collaborative and passionate about unlocking hidden insights in today’s clinical operations landscape and relentless in your pursuit of operational excellence.
• Post Graduate degree with 4+ years of experience or a Bachelor's degree with 6+ years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline). Solid understanding of US and global regulations and guidelines (e.g., FDA, EMEA, ICH) applicable to clinical development.
• Significant experience within the pharmaceutical industry or clinical research organization (CRO) working with clinical data and clinical development processes.
• Deep understanding of complexities of study start up.
• Strong analytical and project management skills.
• Able to rapidly adapt to changes in the work environment, manage competing demands and change approach or method to achieve optimal fit-for-purpose solution.
• Excellence in driving results. You persist in accomplishing objectives and exceeding goals despite obstacles and setbacks, while also helping others to achieve results.
• Excellent verbal / written communication and collaboration skills and ability to influence and build effective relationships in a matrix organization, including to to ensure timely follow-up, issue resolution, and report updates.
• Experience with Veeva clinical solutions and familiarity with leveraging multiple technologies.
• At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
• 401k plan with company matching
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)