- The Fountain Group (Basking Ridge, NJ)
- The Fountain Group are a national staffing firm and are currently seeking a Director , Clinical Safety for a prominent Pharmaceutical client of ours. This ... Length of Assignment: 1 year to start with potential to extend or convert. The Director , Clinical Safety , will be a product safety lead or part of… more
- Merck & Co. (Rahway, NJ)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire ... execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Eisai, Inc (Nutley, NJ)
- …of Data Operations, Data Management, Clinical Safety Data Review and Clinical team. The Assoc. Director of Clinical Programming will oversee the ... is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges in the programming… more
- Formation Bio (New York, NY)
- …role, you'll pioneer the development of sophisticated models to predict clinical outcomes-determining drug efficacy, safety profiles, and optimal indications-to ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (Rahway, NJ)
- …biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process ... Engineer role at the Associate Director level will leverage the individual's leadership, technical, and...and communication skillsets to drive the success of our clinical manufacturing facility and organization. As the facility is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …CSPV to enable/effectively support safety signaling detections and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and ... as R shiny apps for data surveillance, visualization, modeling and simulations, and safety signal detection. Lead the development and validations of R package and/or… 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 ... new products in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well as supporting… more
- Merck & Co. (Rahway, NJ)
- …Oral Formulation Sciences Job Description:Our company's Pharmaceutical Sciences and Clinical Supply (PSCS) organization translates molecules to medicines, working ... to transform drug delivery and manufacturing technology to positively impact patients.The Director of Oral Formulation Sciences will lead a team of scientists and… more
- Genmab (NJ)
- …have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and maintenance ... will be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …drug coding conventions (MedDRA, WHO-DD). preferredExtensive knowledge of FDA regulations, clinical and safety databases, preferredFamiliarity with Good ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… more
- Genmab (NJ)
- …RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early and ... responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- 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 ... digital experience across HCPs, Consumers, and SOC to drive adherence and safety as patients start therapy. Partner with Market Access, Eisai Patient Support,… more
- Merck & Co. (Rahway, NJ)
- …Our company Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be responsible for:Evaluating pre- clinical and… more
- Merck & Co. (Upper Gwynedd, PA)
- …clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... and will interact externally with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and translational work… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …this role, the incumbent will contribute to creation and improvement of Clinical Development processes. Job Description:Execute an overarching safety program ... experience in pharmaceutical industry.At least 2 years in Patient Safety .At least 2 years of experience in Clinical... Safety .At least 2 years of experience in Clinical Development.At least 2 years of Oncology experience. Competencies:An… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to determine risk factors with and for other technical departments (eg, Clinical , Medical, Safety , Data Management, Statistics). This position requires skills ... research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... ED&AA, IT, Ethics and Compliance, Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues. Externally,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Project TeamsGOMA and Specialty MA Management teamsData Management/ Biostats Clinical Safety and PharmacovigilanceR&DVendors/ CROs/ third partiesHEOR/ ... around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV...products whereby MA is in scope for label extension, safety only studies (PH IV studies) and/ or EAP… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... Operations, including but not limited to - Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues, to deliver… more
- New Story Schools (Wyoming, PA)
- Job Title: Clinical Director Location: Wyoming, PA 18644 Employment Type: Full-Time (Monday to Friday) Salary: Based on education and experience Join New Story ... in a supportive school environment. Your Role as a Clinical Director : Clinical Leadership &...staff, while ensuring adherence to best practices in classroom-based clinical care and intervention. Compliance & Safety … more
