Associate Principal, Qualitative Research, QualityMetric/Patient Centered Solutions

Remote, candidates must be based in recruiting countryAbout QualityMetric-Patient Centered SolutionsIQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug / non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science / pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs) / patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment.To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth.About the RoleThis position plays a key role in the scientific advancements in the qualitative patient outcomes research team. Staff in this role must be well-published and have strong expertise in the evaluation, selection, development, and validation of clinical outcome assessment measures for clinical trials and observational studies, and patient-reported outcome (PRO) measures in particular. Experience in developing evidence dossiers and briefing books to support product labeling based on PRO and other COA endpoints consistent with the Food and Drug Administration PRO guidance is required. This position supports a broad range of studies aimed to better understand the patient’s experience related to conditions, their treatments, and the healthcare system. This position has a key role as a decision-maker for growth to new methods and approaches, to develop key relationships for business development and mentor current scientific staff in business development efforts, to mentor senior- and mid-level scientific staff, and assists in developing team best practices and training materials.ResponsibilitiesManaging and contributing to the execution of a large portfolio of PCS COA Consulting projects, in the design, development and delivery of client deliverables and presentations; from project kick off until close, including overseeing the technical and scientific approachesPlanning, organizing and managing resources (internal and external) to bring about the successful completion of specific project goals and objectivesLeading interactions with clients in the pharmaceutical industry for business development; serving as key point of contact with client, and developing relationships through face-to-face discussions or workshops, telephone, and email contactIdentifying opportunities for expansion of PCS COA Consulting service offerings, internal and external to IQVIA, by developing and / or elevating new business opportunities through the identification of follow-on work and new leadsLeveraging business experience and acumen in identifying strategic alternatives and project approach to client questions and to elevate our capabilities to deliver world-class solutions for clientsSharing PCS subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clientsProviding follow-up with client after project deliverable has been completed to ensure client satisfactionSharing information and provide efficient communication with delivery teams, to resolve escalated issuesSupporting the development of intellectual property for use on future engagementsManaging the process of proposal preparation and / or modifications including overall bid integrityDeveloping broader and deeper knowledge of consulting methodologies and pharmaceutical market through on the job experience and trainingProviding direction, advice and intellectual leadership to clients and delivery teams; directing consulting teams through consistent participation in team meetingsProviding high level input to, and ensures the development of, client reports and presentations and delivery of all or significant portions of findings to clientSupporting in PCS community building with activities including recruitment, coaching, management of PCS resources in Europe and network development (both juniors and seniors) to collaborate with for delivery and / or BD purposesYou will contribute to the building of the practice by : Leading ad hoc work streams on critical people-related issues such as recruitment, learning, and developmentDeveloping templates and training materials to streamline and optimize new project start-up and team-member onboardingDeveloping formal Project Management processes for COA Consulting services; training and mentoring Associates, Associate Consultants, Consultants, and Managers in these Project Management processesProviding senior guidance and training to junior-level staffServing as a coach to 3-4 staffAbout YouRequirements : PhD in a relevant field (or Master’s degree with additional experience)8 years post-doctoral experience (or 12 years with Master’s degree)5-8 years professional experience in consulting within the pharmaceutical industryShould be well-published and have strong expertise in the evaluation, selection, development, and validation of clinical outcome assessment measures for clinical trials and observational studies, and patient-reported outcome (PRO) measures in particular.Experience in developing evidence dossiers and briefing books to support product labeling based on PRO and other COA endpoints consistent with the Food and Drug Administration PRO guidance is required.5 years direct experience designing and conducting qualitative research in healthcare industry; prefer experience in life sciences2 years project management experience focused on multinational strategic consulting projectsDemonstrable analytical, interpretative. and problem-solving skillsKnowledge of regulatory guidance documents and scientific guidelines relating to clinical outcome assessmentsUnderstanding of instrument development and validation processAble to draft abstracts, posters, oral presentations, and manuscriptsAble to conceptually fit individual scientific and strategy tasks together to determine how the overall project goal will be achievedAble to design a qualitative analysis plan and generate a report fit for client submissionWell-developed written and verbal communication skills including presentations, chairing meetings, workshop facilitation, business and report writingStrong capability in managing large and / or multiple projects and juggling priorities so that deadlines are met while retaining consistently high quality outcomesExperience working in sizable / multi-disciplined teams and leading staffExperience in developing credible relationships with senior level managers and executives in the pharmaceutical / healthcare industryExcellent interpersonal skills and ability to work effectively with others in and across the organization to accomplish team goalsAbility to contribute to business development through the identification of leads, development of proposals etc.Knowledge of key issues and current developments in the pharmaceutical and healthcare industriesKnowledge of consulting methodologies, tools and techniquesExcellent organizational, time management, and problem solving skillsIn addition to the skills and experience above, candidates should have : Fluency in English (spoken and written)A willingness and ability to travel (generally 2 trips per year, could be more)Right to live and work in the recruiting countryIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.The potential base pay range for this role, when annualized, is $165,100.00 - $306,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and / or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and / or other forms of compensation may be offered, in addition to a range of health and welfare and / or other benefits.To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.EEO Minorities / Females / Protected Veterans / Disabled#J-18808-Ljbffr

Salary : $165,100 - $306,500