Head of Regulatory Strategy, Patient Centered Solutions

Overview

IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical 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 customers (mostly life science/pharmaceutical companies) through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research to capture insights about patient priorities, needs, preferences and experiences. 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.

Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. They have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions.  We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth.

Role & Responsibilities

The Head of the Center of Excellence (CoE) for Regulatory sits within the consulting business of PCS and plays a key role in its global leadership team. This individual is a true expert in both the guidance and the practice of developing strategies and evidence to engage US FDA, the EMA and other regulatory agencies on COA endpoints and the use of PED in a regulatory context. This individual fulfills three key functions: 1) bringing their expertise to bear in proposals, to project delivery, and to customers in support of business growth and impact; 2) developing the regulatory capabilities of the PCS consulting organization through training, process improvement and mentorship; and 3) maintaining an active external profile and involvement in the regulatory landscape for PED.

Key responsibilities are:

Customer-facing activities

Develop and deliver insightful, value-added regulatory strategies that address complex client issues relating to COA endpoints and PEDSupport sales efforts by providing regulatory subject matter expertise to customer meetings and proposalsSupport delivery teams who are executing PCS projects with a regulatory component, and ensure we provide consistently high quality insights and contentSupport billable projects as SME and/or study lead, per study requirements, at 40% utilization or greater

Capability building

Support community building with activities including recruitment, coaching, management of resources and network development (both juniors and seniors) to collaborate with for regulatory delivery and/or business development purposesDirectly line manage a small global team of regulatory specialistsMentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clientsProvide training, templates, and oversight to upskill team and ensure consistent high quality consulting and written deliverablesParticipate in annual performance review team processesEngage in recruitment and selection of new staff

External profile

Develop and oversee the PCS thought leadership agenda for the regulatory capability. Represent IQVIA in external working groups and consortiaLead development of IQVIA’s responses to public consultation processes from FDA and other regulatory agencies relating to PEDContribute to the enhanced awareness of PCS in the marketplace, e.g., through speaking engagements, client meetings, and publicationsDevelop and facilitate understanding of emerging regulatory practices, expectations and engagements outside of the US FDA and EMA

In addition, take on other leadership responsibilities as needed, including:

Member of global PCS consulting leadership team and scientific leadership teamProvide regulatory subject matter expertise to the broader PCS organisation (e.g. to instrument ownership and licensing business, and to the implementation services business)

About You

Candidates interested this position will have:

Advanced degrees and 10+ years of experience in patient experience data research, including COA science, preference research, and regulatory engagement (US FDA essential, EMA and other regulatory agencies desirable)Experience working in a regulatory agency and/or demonstrable track record of developing and executing a COA endpoint strategy with successful outcome of COA label claimExperience in developing patient experience materials for regulatory consultations and submissions (e.g. COA dossier, briefing documents for Type B/C/D consultations)An understanding of the global regulatory environment as it pertains to patient experience dataStrong scientific consulting skills and track record of business development in a consulting environmentExperience of medical writing for various audiences, including pharmaceutical companies, healthcare professionals, regulatory bodies and patientsPublications and recognition in the field through participation in industry consortia or scientific bodies. Experienced public speakerWell-developed written and verbal communication skills including presentations, business and report writingAn entrepreneurial nature and interest in developing new client offerings and solutionsDemonstrable analytical, interpretative, and problem-solving skillsExcellent interpersonal skills and ability to work effectively with othersAn ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasksAn ability to establish and maintain effective working relationships in multi-disciplinary and international teamsFluency in English (spoken and written)Willingness and ability to travel from time to timeRight to live and work in the recruiting country

PHYSICAL REQUIREMENTS

Extensive use of telephone communication requiring accurate perception of speech.Extensive use of keyboard requiring repetitive motion of fingers.Regular sitting for extended periods of time.Travel as required.

IQVIA 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. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $209,600.00 - $389,200.00. 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.