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Corporate Counsel
Refer job# MSTH137341
 
Corporate Counsel The candidate will assist with contracting for Firm Innovative Health brand and Firm Essential Health Patient branded aspects of HUB (organizations that assist patients with access and reimbursement for Firm medications) interactions with the field account management teams and field based reimbursement teams or other ancillary roles that interact with patients or patient advocacy groups within the rare disease space. Will assist with contracting for and implementation of HUB vendors for brand funded activities e.g., portal development, eSignature capabilities, text messaging and/or integration with field based roles, plus assisting with review and implementation of Program business rules/rules of engagement guidance and compliance with such business rules; assist with trade distribution agreement preparations/implementation; and assist with government price reporting for various federal price reporting metrics. Review and negotiations the successful candidate will assist with implementation of the legal oversight of HUB, and interaction with such Programs amongst brands and with implementation/integration with field sales/account management with respect to such programs. Integrate with Corporate Affairs and SAS COE clients to support appropriate operations with respect to brand funded HUB, programs and ensure compliance with the recommendations from recent settlements and with Firm s Compliance Program. Responsible for assisting with proactive compliance effectiveness reviews, coordinating with outside law firms that are engaged to conduct such reviews, and supporting the ongoing development and enhancement of brand funding of such Programs and internal policies and procedures to satisfy evolving industry and regulatory compliance requirements within the space in the US. Participates in negotiating and drafting agreements for brand funding of HUB vendors and integration with field based sales, account management and reimbursement support. Expand enterprise legal support to implement additional controls and oversight in the area of brand funding of HUB activities. Draft and revise contractual provisions and implement brand funded HUB activities, such as portal development, eSignature capabilities, text messaging and/or integration with field based roles, plus assisting with review and implementation of appropriate Program business rules and compliance with such business rules for the above activities and assist with enhancement of corporate policy updates, including training and monitoring. Support all aspects of marketing and operations with respect to such brand-funded HUB activities. Provide centralized review and coordination of brand funded HUB activities with those supported by other team members within CSP Legal that support other HUB and reimbursement activities. Provide counsel and implementation support for legal updates for government funded healthcare programs and price reporting metrics along with other CSP Legal colleagues. Support Specialty Access Solutions Center of Excellence with implementation of compliance monitoring and periodic training on evolving issues within the product access space. Prepare and manage preparation of rules of engagement documents and reports on brand-funded HUB activities and integration with field based sales/account management or other ancillary roles that interact with patients or patient advocacy groups within the rare disease space, and participate in activities related to oversight of the Compliance Program as it related to brand funded HUB activities and the rules of engagement with such HUBs by sales/account management or other ancillary roles that interact with patients or patient advocacy groups within the rare disease space. Assist with brand funded HUB program activities, systems, controls and reporting on such programs for the U.S., including: Advising stakeholders on the applicability of federal healthcare requirements relevant to their business activities. Managing contracting and engagement with Drug Safety Unit for CEP program implementation to assure appropriate reporting of adverse events by HUB vendor personnel who are performing services for and on behalf of Firm. Advise on the applicability of federal healthcare regulatory requirements and implications on business activities. Develop and present training related to HUB interactions with sales/account management or other ancillary roles that interact with patients or patient advocacy groups within the rare disease space. Coordinate with Legal and Compliance colleagues to enhance policies and systems controls to address compliance risk areas; interpreting laws, regulations and policies relating to brand-funded HUB activities. Draft and coordinate on preparation of compliance-related reports and presentations for Firm senior management and the Regulatory and Compliance Committee of the Board of Directors related to brand-funded HUB activities. Partner with Compliance to comply with imminent obligations. Provide enhanced oversight, monitoring, SOP development, training related to brand funded HUB activities. Support certification and RAMP process related to brand funded HUB activities. Provide input and expertise to IRO related to brand funded HUB activities. Assist with implementation of changes in regulations in Medicaid, Medicare, 340B and other government programs that are creating complex government price reporting obligations. Work with the trade business colleagues to draft, negotiate and implement distribution agreements with wholesalers and distributors for the PIH and PEH business units.

The candidate must have 12-14 years practicing law or experience in risk management/ compliance in the pharmaceutical or healthcare industry including significant experience with drafting and negotiating contracts and government price reporting. Should have BS or BA degree. JD degree (and admission to practice law in United States) is required. Experience negotiating and/or managing programs related to service agreements under the personal services safe harbor to the anti-kickback statute and regulations and significant experience with US healthcare laws is needed. Understanding of healthcare-related laws and regulations and industry standards required, including the government price reporting under various Medicaid, Medicare, 340B programs, federal false claims act, federal anti-kickback statement, OIG regulations and guidance and pharmacovigilance issues is must. Strong interpersonal skills to work with others within and outside the Company to identify and manage compliance risks are necessary is essential. Deadline: 2/1/2018
 
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