Associate Principal – Patient Centered Solutions

hace 4 semanas


Madrid, España Iqvia Llc A tiempo completo

Associate Principal – Patient Centered Solutions (Quality Metric - IQVIA's business) - Greece/Portugal/Spain/UK
Associate Principal – Patient Centered Solutions (Quality Metric - IQVIA's business) - Greece/Portugal/Spain/UK IQVIA 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 position plays a key role in the scientific advancements in the quantitative patient outcomes research team. Staff in this role must be well-published and have strong expertise in the evaluation, selection, development, and psychometric validation of COA 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.
Role & Responsibilities
As an Associate Principal within the PCS team at IQVIA, you will be responsible for managing or leading multiple consulting projects and ensuring on-time and on-budget delivery for clients in the pharmaceutical or related industries by:
Managing 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 approaches.
Planning, organizing and managing resources (internal and external) to bring about the successful completion of specific project goals and objectives.
Leading 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 contact.
Identifying 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 leads.
Providing follow-up with client after project deliverable has been completed to ensure client satisfaction.
Supporting the development of intellectual property for use on future engagements.
Managing the process of proposal preparation and/or modifications including overall bid integrity.
Providing direction, advice and intellectual leadership to clients and delivery teams; directing consulting teams through consistent participation in team meetings.
Providing high level input to, and ensures the development of, client reports and presentations and delivery of all or significant portions of findings to client.
Supporting 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 purposes.
About You
Candidates interested in joining our Patient Centered Solutions team as an Associate Principal should have:
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 and/or healthcare industry with evidence of career progression.
5+ years direct experience designing and conducting quantitative research in healthcare industry; prefer experience in life sciences.
2+ years project management experience focused on multinational strategic consulting projects.
Demonstrable analytical, interpretative, and problem-solving skills.
Knowledge of regulatory guidance documents and scientific guidelines relating to clinical outcome assessments.
Understanding of instrument development and psychometric validation process.
Proficient in SAS (or similar statistical software).
Well-developed written and verbal communication skills including presentations, chairing meetings, workshop facilitation, business and report writing.
Strong capability in managing large and/or multiple projects and juggling priorities so that deadlines are met while retaining consistently high-quality outcomes.
Excellent interpersonal skills and ability to work effectively with others in and across the organization to accomplish team goals.
Please submit your CV in English.

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