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MAP Program Manager Company & Role Description Founded in 2002, Tanner Pharma Group is a specialty service provider in the biopharmaceutical industry focused on improving patient access to medicines on a global basis. Tanner Pharma offers its biopharmaceutical partners a portfolio of four distinct service offerings that span the product lifecycle from clinical development to commercialization. With its global headquarters in Charlotte, North Carolina and offices in the United Kingdom, Switzerland and Ireland, Tanner Pharma is in a phase of rapid growth. TannerMAP works with pharmaceutical companies to develop and deliver access programs enabling patients with unmet medical needs access to medicines in countries where those medicines are not commercially available. These access programs may be referred to as Named Patient, Expanded Access, Early Access, or Compassionate Use Programs. With a solid foundation established to support future growth, TannerMAP has rapidly expanded its portfolio of programs supporting both big pharma and many small- to mid-size specialty and rare disease companies. To help drive and support this growth, TannerMAP is seeking a Managed Access Program Manager. Role Accountabilities Expected Responsibilities for the Program Manager are: • Design and develop managed access programs through collaboration with prospective pharmaceutical company partners including: *Support in the definition of inclusion/exclusion criteria and other program requirements. *Participate in discussions on overall pricing strategy and implications. *Educate on program regulatory requirements for countries in scope. *Provide input on projected program participation rates. • Support in the development of commercial proposals for managed access program service agreements., • Manage program implementation until fully up and running, including developing and managing a project plan and developing risk mitigation and contingency plans., • Oversee program delivery, manage client relationships, and handle internal and external communication of program performance, including regular client status update meetings., • Develop initial and ongoing program forecast and budget., • Establish high levels of customer service, delivering program specific KPIs and program financial results, and account relationship development objectives., • Troubleshoot and firefight., • Analyze and review prospective program opportunities., • Develop program materials and presentations to support business development or account management activities. Desired Candidate Profile & Capabilities Required: • BS or Master’s degree., • Minimum of 5 years of professional experience in the pharmaceutical industry or consulting, preferably in a market access, commercial, medical, clinical, or R&D role., • Previous experience with the design, setup, and execution of a managed access program preferred., • Clear proficiency in project management skills including ability to develop a project plan, lead periodic review meetings with clients, and hold internal and external parties accountable to meeting deadlines., • Knowledge and interest in oncology or rare diseases., • Basic understanding of the drug development process., • Ability to work cross-functionally and manage multiple stakeholders internally with Tanner and externally with clients., • Pharmaceutical supply chain knowledge helpful., • Proficiency with computer programs including Microsoft Office suite., • Strong command of the English language including concise, clear, and error-free written grammar., • Ability and willingness to travel up to 20%. Soft skills: • Personal Effectiveness: Demonstrating initiative, self-confidence, resiliency, and a willingness to take responsibility for personal actions., • Ongoing Learning: Like ongoing learning and research as part of your daily routine, • Problem-solving: Able to handle difficult or unexpected situations in the workplace as well as complex business challenges., • Project Management: Able to effectively coordinate a project from start to finish; using effective communication, interpersonal skills, and organization to complete projects within defined parameters and timelines., • Results Orientation: The ability to focus on the desired result of one’s own or one’s unit’s work, setting challenging goals, focusing effort on the goals, and meeting or exceeding them. Compensation & Benefits • Salary commensurate with experience £45,000.00-£50,000.00 per year., • Pension scheme (UK), • Private health insurance., • Attractive performance incentive plan., • Vacation, Volunteer and paid sick leave. Tanner Pharma Group’s Core Values: Everything we do at Tanner Pharma Group is dictated by our values. We take them very seriously, and we are proud of this unwavering commitment. Check out http://www.tannerpharma.comto view our core values and learn more about our company. Candidates may be required to organize reference calls upon request. Confidentiality will be respected. Additionally, Pre-employment drug and background screening will be required. Tanner Pharma Group is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

Careers » Clinical Research Associate II (CRA II) As an ISO 9001 certified, organisation PHARMExcel prides itself in delivering high quality and results driven clinical services.Our broad portfolio ranges from non -interventional, CTIMP, ATMP, rare disease and medical devices investigations.You wil

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Your new company My client, a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability and which is focused on improving people's quality of life, specialising in Oncology, neurology and rare diseases, and has a position available for a Pharmacovigilance Patient Safety Partner - Safety Risk Management to join their International Patient Safety team on a 6-month initial contract. Hybrid - 2 days Welwyn 6 Month + Contract Inside IR35 - PAYE - £40 - £50 p/h - Umbrella - £59 - £66 p/h Your new role As the Patient Safety Partner, you will ensure the execution of safety-related activities relevant to the PV (Pharmacovigilance) system through partnership with key stakeholders, meeting regulatory requirements, and ensuring license to operate. Proactively identify opportunities to optimise the PV system. You will focus on the following areas of activities: - Individual Case Safety Reports (e.g. data collection) - Studies, Programmes and other projects with PV implications (e.g., ICT, NIS, PASS, PAES, MAP, PAA, CUP, PTAP, Dicela) You will take on responsibility for assessing PV requirements for organised data collection systems, listed above, with particular emphasis on market research, patient support and digital activities, working with colleagues across the UK business and third parties. You will also conduct Local Safety Risk Management, supporting the Ophthalmology Disease Area: • Identify, analyse and share safety insights by understanding disease areas, engaging with key stakeholders, and ensuring timely, proactive integration into affiliate and global strategies. - Implement global safety solutions locally within the integrated therapeutic strategy and execute product safety launch readiness activities. - Support the country-level risk management strategy to optimise patient outcomes in collaboration within relevant networks and ensure compliant and transparent PV communications (e.g., DHPCs) to healthcare professionals, patients, and external partners in collaboration with Medical Affairs and the cross-functional team. What you'll need to succeed In order to apply for the Pharmacovigilance Patient Safety Partner role, you must possess: -A Degree in life science or healthcare-related discipline (e.g., PharmD, MSc, BSc, Nursing, etc.). -Expert experience in pharmacovigilance, ideally in an affiliate setting. -Experience in supporting Pharmacovigilance for organised data collection systems and experience in local safety risk management planning and implementation -Understanding of decision-making in the local & global PV ecosystem What you need to do now Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on (phone number removed)

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