Program Lead Ii Cdso (Clinical Data Management) Remote

Detalles de la oferta

.Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.Abbvie.Com. Follow @abbvie onTwitter,Facebook,Instagram,YouTubeandLinkedIn. Job Description AbbVie Clinical Data Strategy & Operations is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Aligns DSS study teams with program- and study-level strategies. Assigned programs may include programs that are of low complexity and size. For assigned programs and studies, leads the DSS Study Team and represents DS as a member of the cross-functional study team. For assigned programs and studies, acts as single point of contact and accountable operational lead from DSS. Coordinates associated DSS study teams to meet operational objectives. Engages and connects global functional and cross-functional teams at the study level Interacts with and influences cross-functional team members to achieve program objectives Utilizes operational analytics and project management tools to optimize execution of programs and studies, to manage internal and external resources, to track study progress, and to prepare study status reports. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development. If assigned, participates as the DS study owner in regulatory inspections and internal quality audits. Participates in oversight of vendors and provides feedback related to clinical trial operations, issues, and trends in performance. Responsible for coaching and mentoring team members. Leads DSS innovation and process improvement initiatives and participates in cross-functional initiatives Conducts study execution "lessons learned" across functions May include indirect supervision of employee as well as supervision of work of contract resources. Qualifications Bachelor's degree in scientific or related fields. Advanced degree preferred


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

Requisitos

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