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The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial agreements and investigator grant budgets with study sites. They ensure compliance with internal processes and client expectations while identifying and mitigating legal, financial, and operational risks.
Manage a portfolio of approximately 95 short-term disability claims while providing high-quality customer service to assigned clients. Act as a liaison between the client's leave team and benefits partners to ensure seamless claim processing and continuous process improvement.
The Senior Compliance Investigator leads and oversees enterprise-wide compliance and ethics investigations across all business units and health plans. This role involves assessing allegations, conducting witness interviews, performing root cause analysis, and recommending remedial actions to mitigate risks.
The Regulatory Affairs Specialist is responsible for preparing and coordinating regulatory submission packages to ensure timely approvals in Israel. They also collaborate with quality teams to manage post-market obligations and ensure compliance with regulatory trends and requirements.
Lead consulting engagements focused on Medicare Stars and regulatory performance improvement for health plan clients. Analyze complex data sets and develop actionable strategies to optimize quality measures and operational effectiveness.
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Draft, review, and negotiate agreements with study sites while ensuring compliance with budgetary and contractual parameters. Coordinate with internal functional teams to align site startup activities and achieve target cycle times for site activation.
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