- Merck (North Wales, PA)
- …Under direction from a Director , the Associate Principal Scientist is responsible for implementing regulatory strategies for our organization in ... **Job Description** This Associate Principal Scientist position is equivalent to... will lead the development and the implementation of regulatory strategies for their assigned projects and provide mentoring… more
- Merck (Boston, MA)
- **Job Description** **Job Description** We have an exciting opportunity for a ** Principal Scientist ( Director ) in Translational Medicine** . Translational ... Clinical Research while developing and expanding your career. **Primary responsibilities for the Principal Scientist include the following:** + Key member of an… more
- AbbVie (Irvine, CA)
- …Aesthetics on LinkedIn. The Neurotoxin Research Group at AbbVie seeks an accomplished scientist and leader. The Director /Senior Principal Research ... productive, collaborative, and inclusive laboratory environment in compliance with regulatory and company expectations. Experience managing projects from early-stage… more
- Merck (Rahway, NJ)
- **Job Description** **Device Development Associate Principal Scientist - Development Strategy, Design Controls** **(Associate Director Equivalent)** _Our ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. ** Principal Responsibilities** + Lead/contribute… more
- Merck (Rahway, NJ)
- …**Role Summary** + Under the guidance of a senior leader, a Senior Principal Scientist /Senior Director , has primary responsibility for developing value ... to reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs + In… more
- Bristol Myers Squibb (Cambridge, MA)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… more
- Rochester Regional Health (Rochester, NY)
- Job Title: Senior Principal Scientist Department: Scientific Affairs Location: Rochester, NY Hours Per Week: 40 Schedule: Monday - Friday 9:00 AM - 5:00 PM ... SUMMARY As a part of Clinical Trials Scientific Affairs, the Senior Principal Scientist will lead method selection, development, validation, and implementation.… more
- J&J Family of Companies (Cincinnati, OH)
- …America **Job Description:** We are searching for the best talent for a Principal Scientist /Project Leader located in Cincinnati, OH. Purpose: The Principal ... necessary to competitively position products for domestic and international regulatory approval and clinical adoption. The individual will independently design,… more
- Merck (Rahway, NJ)
- …of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's research facility. The ... Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists… more
- Honeywell (Buffalo, NY)
- As a Principal R&D Engineer/ Scientist here at Honeywell, you will play a crucial role in driving innovation and leading research and development initiatives ... mentor a team of engineers and scientists. You will report directly to our R&D Director and you'll work out of our Buffalo, NY location on a hybrid work schedule.… more
- UTMB Health (Galveston, TX)
- Regulatory Scientist I / II - Institutional Office... Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory Practice ... for the interpretation, documentation and reporting of results. The Regulatory Scientist I / II works in...I / II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies… more
- Lilly (Indianapolis, IN)
- …respective functions but will be coordinated by the Ramp Team Sr. Director . **Key Responsibilities:** Responsible for depth of Small Molecule synthesis knowledge ... strategy effectiveness. Provide proficient data analysis and conclusions considering technical, Regulatory and Quality compliance, and business needs. + Work closely… more
- University of Virginia (Charlottesville, VA)
- The Senior Director , Nurse Scientist is a role model for transformational leadership and is responsible for overseeing the operations and finances of defined ... operational planning, program development and quality assurance/performance improvement. The senior director serves as a leader and mentor both within the department… more
- UTMB Health (Galveston, TX)
- …utilize the US FDA GLP regulations as a reference standard. The Regulatory Scientist II may also function as a Principal Investigator for extramurally funded ... Select Agent Program (FSAP). **JOB SUMMARY** **Function** : The Regulatory Scientist II will be assigned as...Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory… more
- Curia (Hopkinton, MA)
- …raw materials, in-process, end product, and stability samples. The Senior Research Scientist I's principal responsibility is the design, development, validation ... SENIOR RESEARCH SCIENTIST I, ANALYTICAL DEVELOPMENT in Hopkinton, MA Curia...manufacturing facility in Hopkinton, MA and reports to the Director , Analytical Development. Join our talented workforce, where a… more
- Curia (Hopkinton, MA)
- …raw materials, in-process, end product, and stability samples. The Senior Research Scientist II's principal responsibility is the design, development, validation ... SENIOR RESEARCH SCIENTIST II, ANALYTICAL DEVELOPMENT in Hopkinton, MA Curia...manufacturing facility in Hopkinton, MA and reports to the Director , Analytical Development. Join our talented workforce, where a… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are looking for a highly motivated Principal Scientist , Clinical Pharmacology in our Pharmacometrics (PMx) group. The position will report to the Senior Group ... Director (SGD) within Clinical Pharmacology (CP) in the General...into clinical study reports + Provide CP support of regulatory documents, communications, and presentations (eg, IND, health authority… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Bristol Myers Squibb (Cambridge, MA)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …Dermatology is seeking a highly motivated and accomplished MD/PhD or PhD scientist with experience in translational science, human subjects research, and team ... leadership to serve as Associate Director of Research Projects. This position is integral to...of research projects, ensuring compliance with study protocols and regulatory requirements. + Facilitate medical student engagement in departmental… more
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