Senior Associate, Clinical Outcomes Assessment
United States of America, Remote ID de la oferta R0000029675 Categoría Regulatory / Consulting Fecha de publicación 11/22/2024Overview
Como parte de Consultoría de Parexel, cumplirá un rol vital al asistir a las empresas biofarmacéuticas y de dispositivos médicos a transitar el complejo y siempre cambiante entorno regulatorio. Respaldado por su experiencia científica, técnica y regulatoria, trabajará de cerca con los clientes para desarrollar e implementar estrategias regulatorias que colocarán sus medicamentos en el mercado con mayor rapidez y los mantendrán allí.
Valoramos la colaboración, la innovación y el aprendizaje continuo. Como miembro de nuestro equipo, se asociará con un grupo diverso de clientes y estará expuesto a diversos tipos de medicamentos y áreas terapéuticas. Asimismo, desarrollará sus habilidades a través de asignaciones desafiantes y con la mentoría de profesionales experimentados en asuntos regulatorios. Además, disfrutará de la flexibilidad de trabajar en modalidad remota, al tiempo que forma parte de un equipo colaborador y dinámico.
Perfil del éxito
¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?
- Comunicador
- Estratégico
- Constructor de relaciones
- Solucionador de problemas
- Orientado al detalle
- Impulsado por los resultados
Acerca de este rol
We are currently seeking a Senior Associate, Clinical Outcomes Assessment to join Parexel's growing team. This role offers a unique opportunity to support our team of clinical outcome assessment (COA) scientists in the evaluation of discrete event modelling made with patient input. The existing team includes psychologists with a broad range of experience in industry, academia and clinical practice.
As a Senior Associate, Clinical Outcomes Assessment, you will be responsible for COA projects on Instrument validation, Implementation and COA Analyses, Qualitative Interview Studies as well as, potentially, Preference designs including Discrete Choice Experiment survey design and providing strategic input and advice to our clients.
Key responsibilities:
Support Qualitative interviews with Patients, Clinicians and Caregivers, ePRO vendor oversight, Psychometric Validation analyses, Patient Preference and DCE projects.
Design, conduct, and analyze psychometric as well as health-related user preferences studies.
Advocate behavioral science methods more broadly across the Parexel and clients and generalize learnings into a framework that can help bring behavioral science to scale.
Develop proposals and study protocols that include elements of experimental design.
Qualifications:
Ideally a recognized or up and coming expert in the field of COA implementation or validation, demonstrated through publication records, involvement in relevant special interest groups (e.g. ISPOR, ISOQOL).
Minimum of 3-4 years’ experience in COA Validation and Psychometrics, as established by publication records.
Strong scientific and regulatory knowledge of relevant guidelines.
Minimum MSc, PhD preferred in a relevant discipline (e.g. Psychology, Statistics, Outcomes Research).
Fluent in vocal and written English.
Additional languages – highly desirable i.e. Spanish
East Coast Candidates Highly Preferred
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Perspectivas de los empleados
POR QUÉ TRABAJAR EN PAREXEL
