Jill B. Conner, Ph.D. work email
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Jill B. Conner, Ph.D. personal email
Extensive experience working in the pharmaceutical industry engaging with key external stakeholders, managing, leading, and providing life cycle management, study design, clinical operations, project management, and client relation services across several therapeutic areas. I am a result-oriented individual with a strong work ethic, strong organizational and interpersonal skills, with excellent written communication, and presentation skills. I have published research in several therapeutic areas and have a good understanding of pharmaceutical industry practices, clinical trial and investigator-initiated study processes, and compliance measures.
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Field Science Director - Rare DiseaseSanofi Dec 2022 - PresentParis, France, FrLiaise between US Medical Affairs Rare Disease and the Value and Access team and Account Directors.Serve as the medical/scientific lead for healthcare accounts and organizations. Coordinate, develop, and present pipeline, product, and disease state education to healthcare accounts and organizations.Liaise between US Medical Affairs Rare Disease and the Clinical development and Clinical Study Unit team. Partner with clinical development to support clinical trials in work related to the specific disease area and serve as an internal resource for the MSLs on pipeline products. -
Field Medical Scientific Associate Director - Rare DiseaseSanofi May 2021 - Dec 2022Paris, France, FrAssist with the development of the US Medical Plans in association with the US Medical Director, maintaining alignment with the Global Brand goals.Partner with clinical development to support clinical trials in work related to the specific disease area and serve as an internal resource for the MSLs on pipeline products.Partner with market access to provide medical support and presentations to payer audience.Maintain territory and Medical Science Liaison role.
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Medical Science Liaison - Rare DiseaseSanofi Jul 2018 - May 2021Paris, France, FrResponsible for providing non-promotional scientific, educational, and research support for the Genzyme rare disease portfolio in the Midwest. Responsible for developing and maintaining relationships with key rare disease experts and building a well-informed advocacy base for Genzyme’s rare disease franchise.Participates in medical education for healthcare professionals through presentations at office visits, investigator meetings, advisory boards, medical meetings, and other appropriate venues to enhance product and disease state knowledge.Responds to unsolicited requests regarding interest in investigator sponsored studies and supports submissions through appropriate internal processes. Responds to unsolicited requests for medical information associated with supported products and disease states.
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Senior Director Global Life Cycle ManagementTeva Pharmaceutical Industries Ltd. Oct 2011 - Apr 2018Proactively design, obtain approval, and implement LCM strategies (e.g., new indications and formulations, generic defense and regulatory strategies), starting at approximately Phase II of a product’s development through the life of the product for the Global Branded Specialty Group’s CNS and oncology assets. Document the decisions regarding the LCM strategies, their priorities, and manage the budget for the department LCM activities. Establish and lead LCM and ad hoc teams, as necessary, to support execution of LCM strategies. Collaborate effectively with team members in establishing and monitoring action plans for teams to ensure timely deliverables.
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Director Medical OperationsTeva Neuroscience Mar 2006 - Oct 2011Tel-Aviv, IlProvided leadership, management, guidance, training, support, and technical expertise to the Medical Operations Associates and their teams. Responsible for the development and design of research strategies that addressed the needs for Teva Pharmaceutical’s products and for ensuring the Medical Operating Plan was developed and executed optimally by overseeing the project management, budget, and execution of all clinical trials, investigator initiated trials, and outcomes research studies. -
Director Project Management/Clinical OperationsUnited Biosource Corporation 2001 - 2006Blue Bell, Pa, UsResponsible for the planning, project management and delivery of the clinical component of all projects in accordance with the scope of work and contracted timelines. Managed all clinical departments including Project Management, Clinical Monitors, Call Center, Medical Monitors, and Central Pharmacy.
Jill B. Conner, Ph.D. Skills
Jill B. Conner, Ph.D. Education Details
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Trident University InternationalHealth Sciences - International Health -
Baker UniversityManagement
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University Of Missouri-Kansas CityMedical Technology
Frequently Asked Questions about Jill B. Conner, Ph.D.
What company does Jill B. Conner, Ph.D. work for?
Jill B. Conner, Ph.D. works for Sanofi
What is Jill B. Conner, Ph.D.'s role at the current company?
Jill B. Conner, Ph.D.'s current role is Field Science Director - Sanofi.
What is Jill B. Conner, Ph.D.'s email address?
Jill B. Conner, Ph.D.'s email address is ji****@****arm.com
What schools did Jill B. Conner, Ph.D. attend?
Jill B. Conner, Ph.D. attended Trident University International, Baker University, University Of Missouri-Kansas City.
What skills is Jill B. Conner, Ph.D. known for?
Jill B. Conner, Ph.D. has skills like Clinical Research, Clinical Trial Management, International Project Management, Gcp, Oncology, Clinical Development, Project Management, Ctms, Cro, Clinical Trials, Project Planning, Market Access.
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