Director Biomarker Informatics - Oncology - New Brunswick, NJ
Lead a team focused on the development of personalized medicine utilizing your expertise in translational medicine, biomarker discover, companion diagnostics, and patient population identification.
Develop Preclinical Strategies to optimize patient selection;
*** Analyze and interpret genomic, transcriptomic, proteomic, metabolomic, and pharmacogenomic data sets derived from patient samples, databases and medical monitors
Title: Global Program Regulatory Manager
Company: Pharmaceutical Company
Location: Northern NJ
Status: Direct hire
The GPRM works with some independence under limited supervision to provide strategic and operational regulatory direction and may support the DRA global program team (GPT) representative and/or GTAL for programs through development, registration and approval/post approval. The GPRM ensures the execution of regulatory plans in ...
Under supervision, provide strategic and operational global CMC regulatory direction and documentation for projects/products covering development, registration and approval/post approval activities. The following activities may be performed within this capacity:
Provide and/or implement global CMC regulatory strategy for development projects or marketed products
Lead or contribute to global CMC submission activities (planning, authoring, reviewing, coordination, submission) for ...
Play a pivotal role in the advancement of molecular biology research and development by coordinating, supporting, and overseeing the completion of projects involving:
*** Small animal husbandry
*** Biological sample preparation and grafting
*** Grafted sample growth
*** Sample validation and preparation for shipping
*** Shipping completed sample to clients
Candidate must possess at least 3 years experience at the bench level performing similar duties or in an administrative capacity ...
Plan, coordinate, and oversee the completion of high volume rodent xenografting, growth, preparation, and preservation projects at a major molecular biology organization.
*** 3+ years of similar work with rodents or similar laboratory animals.
*** BS or MS in a related scientific field
*** Familiar with correct procedures with respect to husbandry requirements as specified by the Association for Assessment and Accreditation of Laboratory Animal Care
*** Ability to troubleshoot and ...
*** Knowledge of animal research procedures and practices.
*** Experience with heterografts or xenografts in a molecular biology environment.
*** History of successful scientific project administration.
*** Ability to effectively manage the logistical aspects of rapid, high volume projects. (project coordination, scheduling, etc.)
Shall champion consistently revolving projects focused on grafting of client supplied entities, growth, preparation, and shipping of biological entities ...
Job Ref: #1637
Location: Parsippany NJ
Salary: Dependent on candidate.
Summary: Growing environmental consulting firm looking for a regulatory compliance specialist with 10+ Years of experience. We are seeking a professional with project experience to ensure environmental permitting, periodic reporting, training, and other compliance obligations relevant to a specific site are met on a consistent and timely basis. This is a leadership position with technical ...
Seeking a strategic expert in the respiratory disorder field with a successful track record planning and managing all preclinical activities of novel protein therapeutics and establishing pharmaceutical and academic collaborations.
Shall manage a team of up to 10 scientists in target discovery, biomarker development, antibody generation, mechanism-of-action studies, and in vitro & in vivo models.
Requires PhD and 10+ years of respiratory biology experience.
Enjoy the career path opportunities ...
Representation of GLF on cross-functional Project Teams (early or full development) under appropriate guidance; responsible for design and co-ordination of pharmacokinetic ele-ments of preclinical and/or clinical development plans and regulatory documentation; assures that the pharmacokinetic support to all assigned projects is optimal in quality, timing and cost; ensure appropriate input to the early development team and/or later stage teams; evaluates in-licensing opportunities upon request and is ...
Apr 29 -
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