- WSP USA (Morristown, NJ)
- …teammates from across the globe. WSP is currently initiating a search for a ** Sr . Technical Manager - Electrical Engineer** to support our **Oradell, NJ** office. ... independently to provide guidance and leadership to mid-level to senior level team or project members, with strict adherence...safety and ability to abide by WSP's health, safety and drug /alcohol and harassment policies. +… more
- Balchem (Montvale, NJ)
- Sr . Global Operational Excellence Manager Department: Corp Operations Location: Montvale, NJ Start Your Application ... stable and growing company, visit www.balchem.com POSITION SUMMARY: The Operational Excellence Manager is expected to be the leading LEAN subject matter expert for… more
- Taiho Oncology (Princeton, NJ)
- …Hybrid Employee Value Proposition: Join our dynamic and expanding mid-size company as a Sr . Manager , Regulatory Affairs Strategy. In this role, you will support ... directs global regulatory affairs activities and provides regulatory guidance during drug development, approval and post approval processes and commercialization, in… more
- Taiho Oncology (Princeton, NJ)
- …Employee Value Proposition: Embark on a transformative journey with Taiho Oncology as a Senior Manager , Global Labeling and PV Operations. At the forefront of ... you'll have the opportunity to shape the future of drug safety , contribute to groundbreaking research, and...experience in our rapidly evolving organization. Position Summary: The Senior Manager , Global Labeling Innovation & PV… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …researching on real-world evidence, and creating hope for all facing illness. The Senior Manager , Supply Chain leads, develops, establishes, and manages the ... functions (Quality Assurance, Regulatory Affairs, Marketing, Market Access, Medical Affairs, Drug Safety , Finance, etc.), colleagues in Tanabe Pharma group,… more
- Taiho Oncology (Princeton, NJ)
- …and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ensuring assigned clinical studies ... procedures and oversees the quality of the data and safety of the patients. Communicate deviations from the protocol,...Work with internal and external functional teams to ensure drug accountability is managed at study sites and that… more
- Bristol Myers Squibb (Madison, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician sits within Clinical Development, which is a ... organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution,… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …product(s). Examples include meeting requests, briefing packages, original Investigational New Drug (IND), IND amendment, and routine submissions (eg, Development ... Safety Update Reports / DSURs, Investigator Brochure/ IB updates,...or more Gilead therapeutic areas and varying stages of drug development is strongly preferred. + Demonstrated ability to… more
- Parexel (Trenton, NJ)
- **CRA and Sr CRA positions- Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility ... + Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study...Science Liaisons (MSLs) as directed by LSAD or line manager . **Compliance with Sponsor Standards** + Ensures compliance with… more
- Taiho Oncology (Princeton, NJ)
- …off on clinical documents related to clinical studies as outlined by the manager . + Attend study site initiation visits (SIV) and provides therapeutic area, ... the CRS on an ongoing basis. Review of the safety data will be done through data listings and...study conduct and operational risks. Represent the molecule at senior management governance meetings. + Co-responsible with Clinical Development,… more
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