- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Director , HCP Marketing, Alzheimer's Disease will lead several core marketing, strategy, and lifecycle ... planning projects focused on the upcoming subcutaneous launch and the subsequent preclinical indication. This role represents a key opportunity for a talented,… more
- Eisai, Inc (Exton, PA)
- …If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and building a ... (ADI) production processes for new products in development through their lifecycle ( Preclinical through phase III clinical development) at the Biologics Pilot Plant… more
- AbbVie (North Chicago, IL)
- …services in our Allergan Aesthetics portfolio. Description: The Department of Pathology in Preclinical Safety (PCS) at AbbVie has an outstanding opportunity for ... a Director -level Board-Certified Veterinary Anatomic Pathologist. The successful candidate will lead the design and implementation of pathology strategies for… more
- AbbVie (North Chicago, IL)
- …Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: Serves as a safety pharmacology strategist for assets across AbbVie's portfolio. Responsible for ... the overall strategy and execution of the safety pharmacology strategy, collaborating cross-functionally with project leads, communicating decision-enabling data… more
- Touro University (Hawthorne, NY)
- …Director at the Touro College of Dental Medicine and indirectly to the Director of Preclinical Education, Preclinical Faculty. Responsibilities + Attend ... of Dental Medicine invites applications for part-time (2 days/week) Preclinical Faculty in the Touro Dental Clinic. The ...Make lectures and presentations as requested by the Course Director . + Are familiar with and abide by all… more
- Catalent Pharma Solutions (San Diego, CA)
- **Title: Director Product Development** **About Catalent San Diego:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) ... GMP (Good Manufacturing Practices) manufacturing and stability storage and testing for Preclinical through Phase 2 programs. At Catalent San Diego, we recruit and… more
- Merck (West Point, PA)
- …PK/PD modeling and simulation to support dose selection, design of PK/PD and safety assessment studies, and dose justifications for preclinical and clinical ... strategic decisions from lead selection through filing and life-cycle management. As Director in the West Point DMPK group, your main responsibility is leading… more
- J&J Family of Companies (Cincinnati, OH)
- …The individual will contribute to the design, execution, analysis and interpretation of preclinical studies to understand the safety and efficacy of product ... preclinical scientific input on the evaluation of physical safety and efficacy for technologies and products at all...Execution: + Functions as a Good Laboratory Practices Study Director when designated. + **As Study Director **… more
- J&J Family of Companies (Spring House, PA)
- …therapy, biologics, and RNA therapeutics. The incumbent will collaborate with the preclinical science and translational safety team to develop the translational ... Description:** Johnson & Johnson is recruiting for a Senior Director , Head of Mechanistic Pharmacology, located in Spring House,...pharmacology strategy and execute early safety risk assessment assays through technology innovation and lab… more
- University of Utah (Salt Lake City, UT)
- …**Job Title** PS Assoc Dir, Rsrch & Science **Working Title** PS Associate Director of Research and Science **Job Grade** H **FLSA Code** Executive **Patient ... needs are met. 4. Assumes authority and performs functions of the department director in his/her absence. 5. Participates in the development and interpretation of… more
- Charles River Laboratories (Shrewsbury, MA)
- …Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art ... marketing at local Charles River sponsored meetings on request. * Preclinical function: Participate in cross-site initiatives related to scientific initiatives,… more
- Actalent (Cranbury, NJ)
- Job Title: Director of Drug Discovery Job Description We are seeking a highly skilled Director to join our pharmaceutical research team. This role involves ... position includes managing a team of approximately five direct reports. This is a director -level opening, but the title could vary from senior manager to executive … more
- Charles River Laboratories (Memphis, TN)
- …you can feel passionate about. **Job Summary** Reporting to the Site Director , the Associate Director , Biomanufacturing Operations is responsible for managing ... provides for the manufacture of drug substance and drug product. The Associate Director is responsible for ensuring that all staff is appropriately trained and… more
- Charles River Laboratories (Mattawan, MI)
- …Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art ... can feel passionate about. **Job Summary** The Human Resources Director will serve as the strategic HR partner and...strategic HR partner and site HR leader for the Safety Assessment business at the Mattawan, Michigan site. As… more
- Charles River Laboratories (Reno, NV)
- …Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art ... a career that you can feel passionate about. **Job Summary** The Associate Director of Laboratory and Logistics position at Charles River Laboratories in Reno, NV… more
- Charles River Laboratories (Memphis, TN)
- …a career that you can feel passionate about. **Job Summary** The Director Microbiology and Sterility Assurance be responsible for all strategy, process, compliance, ... cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone… more
- Lake Erie College of Osteopathic Medicine (Jacksonville, FL)
- …of Year I and Year II of the curriculum as well as those components of preclinical education that occur in Year III and IV of the curricula. Oversees and directs the ... faculty, oversees the entire Year I and Year II preclinical education program as well as those components of...practices; + Compliance with state and federal regulations and safety protocols; + Knowledge of patient's ("HIPAA") and student's… more
- Bristol Myers Squibb (Princeton, NJ)
- …scope. **Role & Responsibilities:** + Serve as the New Jersey Radiation Safety Officer (RSO) on BMS's Radioactive Materials Licenses #507395 and #691580. ... and approved by NJDEP. + Serve as the Cyclotron Particle Accelerator Safety Officer (PASO). Regulatory qualifications/requirements to be eligible as a PASO are… more
- Charles River Laboratories (Shrewsbury, MA)
- …Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art ... regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols]. * Represent the site to government,… more
- Charles River Laboratories (Wayne, PA)
- …requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols]. ⦁ Communicate all identified compliance ... cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone… more
