- Veterans Affairs, Veterans Health Administration (Miami, FL)
- …Clinical Laboratory Scientist : vacareers.va.gov/wp-content/uploads/sites/5/Total-Rewards-of-a-Medical-Technologist-Career-Flyer.pdf The ... The CLS maintains all certifications required of a clinical laboratory scientist . Applies knowledge of compliance requirements for laboratory functions. In addition… more
- Merck (Rahway, NJ)
- **Job Description** **JOB DESCRIPTION SUMMARY** The Associate Principal Scientist is a DVM/VMD and/or PhD whose primary function is to design, coordinate, ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and… more
- L'Oreal USA (Clark, NJ)
- …partners (CROs/external vendors, global Advanced Research, Applied Research, Safety and Regulatory Affairs , Technology Incubators, and skin and hair care ... Home (https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 206467 Associate Principal Clinical Research Scientist , Open Clinical Innovation… more
- Abbott (Santa Clara, CA)
- …stake holders including clinical project management, clinical operations, biostatistics, data management, regulatory affairs , medical affairs as well as ... Santa Clara, CA, currently has an opportunity for a Principal Clinical Scientist ** to join our ONSITE...analyze statistical analysis plans + Generate documents to support regulatory submissions for Abbott products and/or respond to questions… more
- J&J Family of Companies (West Chester, PA)
- …Switzerland **Job Description:** We are searching for the best talent for a Principal Scientist , Clinical Research located in West Chester, PA. Purpose: ... relevant CR&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , HEMA, R&D, etc.), ensuring cross-… more
- J&J Family of Companies (Spring House, PA)
- …more at https://www.jnj.com/innovative-medicine **We are searching for the best talent for a Principal Scientist , Muscle Biology - Aging & Metabolism to be in ... Spring House, PA or Cambridge, MA.** **Purpose:** The Principal Scientist plays a pivotal role in shaping drug discovery and translational research strategies to… more
- AbbVie (North Chicago, IL)
- …with many groups external to PDS&T, for example: Manufacturing Operations, Regulatory Affairs , Quality Assurance, etc. Responsibilities: . Effectively functions ... countries. AbbVie Product Development Science & Technology (PDS&T) is seeking a Principal Research Scientist , Peptide Chemistry to conduct late-stage development… 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 evidence ... incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may… more
- J&J Family of Companies (San Diego, CA)
- …championing patients every step of the way. We are searching for a **Senior Principal Scientist , Computational Multiomics, Precision Measures** , to be in either ... approaches in this setting + Engage with Clinical Development, Global Regulatory Affairs , Data Science & Digital Health, Patient Reported Outcomes, Statistics to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Drug Metabolism & Pharmacokinetics, Translational Medicine & Clinical Pharmacology, CMC, Regulatory Affairs , Patient Safety and Pharmacovigilance to implement ... authorities and will consolidate safety data from nonclinical studies into regulatory submissions as needed. In addition, integrated safety assessments may also… more
- AbbVie (North Chicago, IL)
- …engineers, pilot plant engineers, drug product development scientists, program managers, and regulatory affairs specialists. + Author publications and present at ... chain for pipeline molecules and help prepare and defend CMC regulatory content. Chemical/Bio Engineers within Process Engineering support pipeline projects through… more
- Bristol Myers Squibb (Cambridge, MA)
- …the PC space + Manages relationships with key internal stakeholders including Regulatory , Clinical, Commercial, Medical Affairs & Communications and external ... after clinical proof-of-concept studies, including but not limited to regulatory submissions and life-cycle management. Translational disease strategies in… more
- HNTB (Boston, MA)
- …design, and construction of proposed projects. + Serves as task lead or principal author in the preparation of reports, on environmental science effects of projects. ... for local, state, and federal environmental permits as well as other regulatory compliance laws and regulations. + Organizes and participates in public meetings.… more
- HNTB (Boston, MA)
- …design, and construction of proposed projects. + Serves as task lead or principal author in the preparation of reports, on environmental science effects of projects. ... for local, state, and federal environmental permits as well as other regulatory compliance laws and regulations. + Assists in organizing, preparation, public… more
- AbbVie (Irvine, CA)
- …software, electrical, and systems engineering teams, as well as quality assurance and regulatory affairs , to ensure seamless product integration. + Stay abreast ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description We are looking for a Principal Research Scientist I to join our Devices and Combination Product… more
- Abbott (Santa Clara, CA)
- …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well as ... position will have significant interaction with executive leadership, physicians and regulatory authorities. Furthermore, this position will be required to execute… more
- Merck (Boston, MA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
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