- IQVIA (Boston, MA)
- …training and experience Req + Preferred: Experience selling full service clinical trial services to small/mid-sized biotech companies in the New England region. + ... Proven track record at mid-level and high-level contacts. + Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business + Solid understanding of the principles of drug discovery, development, and… more
- Lilly (Indianapolis, IN)
- …following: * Articulating the flow of data (structure and format) from clinical trial participant to analysis and applying this knowledge to data standards and ... solutions. * Technology platforms (system/database) for data acquisition and aggregation. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require… more
- Lilly (Indianapolis, IN)
- …drug development. The Foundry's mission is to accelerate innovation, expand clinical trial capacity, expedite the delivery of new medicines, and reduce costs and ... environmental impact. The Process Translation and Execution (PTE) team drives scientific excellence and innovation to accelerate manufacturing advancements. The team translates API/DS process knowledge into clinical supply readiness, oversees technology… more
- Boehringer Ingelheim (Ridgefield, CT)
- …sharing, improvement, innovation, accountability, and collaboration to accelerate clinical trial delivery and maximize value for investigational sites, patients, and ... the organization. **Duties & Responsibilities** * Develop and implement a global early phase Medical Writing excellence strategy that simplifies processes, sharpens focus, and accelerates clinical development across all Therapeutic Areas. * As part of the… more
- ThermoFisher Scientific (Wilmington, NC)
- …research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve ... health outcomes that people and communities depend on - now and in the future.** **Location/Division Specific Information:** Join Thermo Fisher Scientific as a Global Medical Safety Lead Physician(FSP) based in the United States and be part of a world-class… more
- AbbVie (Irvine, CA)
- …a global scientific and business strategy. *Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and ... experience in development of clinical strategy and the design of study protocols. *Must possess excellent oral and written English communication skills. *Ability to exercise judgment and address complex problems and create solutions for one or more projects.… more
- ThermoFisher Scientific (Wilmington, NC)
- …research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve ... health outcomes that people and communities depend on - now and in the future. Evidera's Patient-Centered Research (PCR) group is responsible for patient experience and insight research to support product development. Our work has helped identify and clarify… more
- Taiho Oncology (Princeton, NJ)
- …studies). Participates in the development, execution, and management of Investigator Sponsored Trial (IST) strategy for all products and pipeline. Works closely with ... National Comprehensive Cancer Networks on Oncology Research Programs. + Responsible for facilitating publication strategy and plans (Clinical, Medical and EVD), medical communication and medical information planning and execution. Collaborates across the… more
- Chiesi (Boston, MA)
- …research in rare diseases or + Experience in Clinical Development (clinical trial design, conduct and interpretation) Education + Medical Doctor Degree is required; ... + Preferred Specializations (not binding), Pediatrics, Neurology, Neuropsychiatry + Past experience in Rare Diseases is desirable as well as in development of treatment for rare pediatric/neurologic indications is considered a plus Compensation The annual base… more
- AbbVie (North Chicago, IL)
- …the Safety Management Plan and relevant safety chapters/text of key clinical trial documents such as informed consent, protocols (specifically inclusion / exclusion ... criteria, Adverse Event management and reporting, and AEs of interest). + Evaluates all safety data generated in clinical trials on a contemporaneous basis. + Provide medical leadership on global teams on safety related issues. + Responsible for overall… more