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Biotech Jobs in New Jersey

1000+ jobs

Job Number: 435916 Program Manager, Clinical Development OVERVIEW Reports to the Director, Clinical Development and supports various activities within Clinical Development, including: Content development and review of Protocols, ICFs, and CSRs . Manage and conduct clinical data review and protocol deviation review/evaluation. Author Clinical sections of regulatory documents (IND annual reports/...
We have an immediate position for a “eTMF Specialist” with our top pharmaceutical client, if you are interested please send your updated resume to greg @ collabinfo.com orcall me at 732-788-3483 Title: eTMF Specialist Duration: 8+ Months Location: Princeton, NJ Essential Job Duties: · Function as Designated Project Team Member to whom a lead data manager may delegate eTMF-related tasks. · Sc...
Soils Laboratory Technician Job Description TRC Companies, Inc. (NYSE: TRR) is an engineering, consulting, and construction management firm that provides integrated services to the Environmental, Energy, Infrastructure, Transportation and Real Estate markets. Our multi-discipline project teams provide turnkey services to help our clients implement complex projects from initial concept to deliver...
Description A part time clinical laboratory director is needed for a Physician’s Office Laboratory. The laboratory director must be qualified by CLIA/CLIS to direct high complexity testing in the general immunology and routine chemistry specialties. Duties The laboratory director is responsible for the overall compliance of the laboratory with federal and state guidelines. This includes: Revie...
We currently have an excellent opportunity for a Laboratory Technician-Analytical located at our Ewing, NJ headquarters The Laboratory Technician will perform analytical testing following established procedures providing accurate testing results in a timely fashion. The Laboratory Technician will learn new testing procedures as required under the supervision a chemist or scientist. The Laboratory...
JUNIOR REGULATORY DOCUMENTATION SPECIALIST REQUIREMENT #16-00182 RECRUITER: TYLER HABIB JOB LOCATION: HOPEWELL, NJ JANUARY 29, 2016 Responsibilities: Preparation of CMC elements of regulatory filings Plan the authoring and review of CMC Regulatory documents Working in collaboration with GRS CMC teams and BD technical experts. Creates final drafts of Regulatory documents for submission to G...
Summary: Reports to the Director, Clinical Development and supports various activities within Clinical Development, including: Content development and review of Protocols, ICFs, and CSRs . Manage and conduct clinical data review and protocol devation review/evaluation. Author Clinical sections of regulatory documents (IND annual reports/DSUR/PSUR, briefing books, etc.). Manage clinical progra...
PROGRAM/PROJECT MANAGER WITH CLINICAL DEVELOPMENT REQUIREMENT #16-00258 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ FEBRUARY 11, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Reports to the Director, Clinical Development and supports various activities within Clinical Development, including: Content development and review of Protocols, I...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
ASSOCIATE CLINICAL SCIENTIST REQUIREMENT #16-00173 RECRUITER: MEGAN STRAWN JOB LOCATION: HOPEWELL, NJ JANUARY 28, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: We are seeking a Research Scientist with knowledge and background in molecular biology to develop, validate and test molecular assays in clinical trial samples. Members of the Clinical Mole...
PBMC SCIENTIST REQUIREMENT #16-00172 RECRUITER: JESSICA CLARK JOB LOCATION: HOPEWELL, NJ JANUARY 28, 2016 Project Description: We are seeking a scientist to fill an open position in the PBMC production group within biomarker technologies. The primary focus of this team will be processing high quality PBMC samples from whole blood of patients on various clinical trials for downstream flow cyt...
The Clinical Project Manager (CPM) will work in a matrix management environment and serves as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for spon...
Summary: The Senior Clinical Research Associate (Sr CRA) participates in the conduct of single and multi-center clinical research studies, presents at monitor training meetings and investigator meetings, monitors recruitment and overall study progress, addresses issues as they arise within the realm of the Sr. CRA position, and makes decisions with the guidance of the Clinical Research Manager (C...
I. ROLE SUMMARY: Responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of quality studies, including in process quality control activities. II. PRIMARY JOB RESPONSIBILITIES: Primary responsibilities of this position include: Supports the Clinical Trial Management/operational study teams in the exe...
Manager Praluent GHEOR Lead Job description Support large volume of activities in the PCSK9 Global Health Economics & Outcomes Research (GHEOR) department for alirocumab. Overall the position will support the GHEOR Leads to ensure successful planning and implementation of Global MA strategies in preparation for launch. Define and discuss the operational requirements within Global VE & MA and be...
BIOSTATISTICIAN WITH CLINICAL TRIAL EXPERIENCE REQUIREMENT #16-00251 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ FEBRUARY 10, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: This position is for a contractor statistician. Under general direction, provides statistical support in the design and analysis of clinical trials. Reviews statistic...
Analytical Chemist Requirements: - B.S. or Associates Degree in Chemistry - 1-3 years quality control laboratory experience with chemical/pharma - Experience with HPLC - Experience with wet chemistry, titrations, PH meters - Familiar with GMP enviornment -Instrumentation techniques, for inorganic, elemental analysis, and physical characteristics preferred. -Working knowledge of PGM (platin...
ASSOCIATE DIRECTOR, R&D SOURCING REQUIREMENT #16-00153 RECRUITER: BRIDGET BURNS JOB LOCATION: JERSEY CITY, NJ JANUARY 27, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The Associate Director, R&D Sourcing - Clinical Services will actively support the development and implementation of strategies for the Client clinical services sourcing categories....
DRUG SAFETY ASSOCIATE MUST HAVE PHARMACEUTICAL EXPERIENCE REQUIREMENT #16-00245 RECRUITER: ANITA JORDAN JOB LOCATION: JERSEY CITY, NJ FEBRUARY 9, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Working closely with the Drug Safety Specialists, processes complaints for the fulfillment of regulatory reporting responsibilities for product complaints. ...
The following are the duties and responsibilities. Technology Transfer of ANDA Products under guidance. Manufacturing of Site Transfer Exhibit Batches for filing purpose. Manufacturing and Packaging of Process Validation batches under guidance. Support production in trouble shooting. Preparation of Manufacturing Batch Records, Packaging Batch Records for Exhibit Batches, Commercial Batches an...