Senior Manager- Clinical Operations
- Support regular sponsor/CRO/partner level meetings with operational clinical expertise and strengthen stakeholder engagement through building credibility and delivering against sponsor/CRO/partner needs
- Ensure data currency to deliver desired insights and metrics to sponsors
- Serve as a subject matter expert in clinical research and be a champion for sites
- Support study selection, partnering with the Life Science team to review new study protocols and assess fit for our network
- Collaborate with manager on protocol feedback to maximize site interest and performance
- Manage customer relationships across a diverse group of stakeholders at sponsors, CROs and sites
- Act as the voice of the customer and collect feedback to drive continuous improvement across all functional areas within IH
- Work closely with sponsor and CRO to find efficiencies to optimize site activation timelines
- Communicate risks clearly and recommend resolution strategies, escalating (both internally and externally) as appropriate
- Identifying blockers and trends, as related to site activations and recruitment and helping cross-functional teams troubleshoot
- Facilitate fireside chats and webinars with customers
- Travel as needed to conferences, investigator meetings and to support sponsors during site visits
- At least 8 years experience with phase 2-4 pharma-sponsored clinical trials, including study start-up, CDA, feasibility, regulatory/standard operating procedures, study protocols, and regulations governing clinical research
- Experience coordinating, evaluating, and following patients' participation through clinical trials
- Demonstrated ability to manage multiple projects, meet deadlines, manage risk and adjust priorities appropriately in a clinical study setting
- Demonstrated stakeholder management skills
- Capability to work with new tools and technology
- Willingness to travel to customer sites (~30%)
- Knowledge and experience in the GI & Hepatology clinical trial space
- Prior project and/or program management experience
- 5+ years as a Clinical Research Associate, Clinical Research Coordinator or 3+ years as a Clinical Team Manager
- Experience with CTMS systems - RealTime highly preferred
- Experience working within a start-up organization
- Medical, dental, and vision insurance
- Life and disability insurance
- Parental leave
- Stock options
- Flexible work hours
- Unlimited paid time off
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