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R & D Jobs in Clifton, New Jersey

472 jobs

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...
Our client is a reputable pharmaceutical company in need of a Safety Systems Analyst with experience in drug safety systems and data management. Please review the qualifications below and reply with an updated resume ASAP, as this is an IMMEDIATE need! This is a 1 year+ contract offering up to $47 per hour (W-2), based upon experience. Requirements: · Bachelor's degree required · At least 3-5 ...
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...
Job Number: 435706 Sr.Site Start-Up Specialist OVERVIEW The Site Start-Up Specialist is responsible for executing study start-up for assigned protocols with the goal of meeting study start-up timelines. Monitor project plans to meet Site Initiation Readiness at the Investigator Meeting. Ensure the accuracy and quality of deliverables from clinical team and vendors. Maintain project metrics and...
Summary: This position is for a contractor statistician. Under general direction, provides statistical support in the design and analysis of clinical trials. Reviews statistical aspects of clinical study protocols and reports, and prepares the relevant sections for inclusion in both document types. Develops and executes statistical analysis plans, interprets the results, and generates tables, list...
Requirements: -Bachelors in Life Sciences -3 years’ experience as a Study Start-Up Specialist -Knowledge of FDA regulations Responsibilities: -Collect Essential Documents for assigned studies in startup -Maintain Essential documents and updates for ongoing studies -Execute study start-up for assigned protocols within timelines by identifying clinical team needs, contracting and managing ven...
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...
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. ...
SITE START-UP SPECIALIST REQUIREMENT #16-00140 RECRUITER: BRIDGET BURNS JOB LOCATION: JERSEY CITY, NJ JANUARY 26, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The Site Start-Up Specialist is responsible for executing study start-up for assigned protocols with the goal of meeting study start-up timelines. Monitor project plans to meet Site Initiat...
MANAGER CLINICAL CMC PLANNING REQUIREMENT #16-00071 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ JANUARY 11, 2016 Project Description: The Manager, Clinical and CMC Planning is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study and CMC timelines, providing evaluations of potential risks and conflicts, supporting the team...
Requirements: -Bachelor’s in life sciences or related field -At least 3 years’ experience in as Study Start-Up Specialist or equivalent role Responsibilities: 1. Delivers Business Results -Collect Essential Documents for assigned studies in startup -Maintain Essential documents and updates for ongoing studies (1572, PI CV, Financial Disclosure, Protocol Signature Pages, etc. ) -Execute stud...
Clinical Trial Assistant Requirements: -Associate degree -1-2 year relevant experience in pharmaceutical industry or CRO -Experience supporting clinical trials preferred Responsibilities: -Supports the Clinical Trial Management/operational study teams in the execution and delivery of studies -Support study feasibility activities and perform database/web searches for sites as needed. Work cl...
Associate Director, R&D Sourcing Requirements: -Bachelor’s degree in business or relevant technical discipline. Preferred: Masters Degree in relevant field and/or Juris Doctorate (JD) -Minimum of 10 years in biotechnology/ pharmaceutical industry or equivalent experience. -Minimum of 3 years direct experience in a clinical/functional outsourcing/contracts function. Ideally, with direct engagem...
Senior Project Manager Requirements: -A Bachelor’s Degree in Life Sciences or Engineering discipline; Advanced degree preferred -Project Management experience is crucial -7 years’ experience in pharmaceutical R&D environment or equivalent is required, combined with either/or experience above a minimum of 3 years’ experience in project management, leading multi-disciplinary project teams throug...
OVERVIEW The Manager, Clinical and CMC Planning is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study and CMC timelines, providing evaluations of potential risks and conflicts, supporting the team on proactively resolving potential deviations, and presenting clear timeline reports. This person will work in a team orientated environm...
Seeking a Clinical Research Scientist for a contract working in East Hanover, NJ •Must have direct trial management experience either in assisting a clinical trial leader or acting in the position as a clinical trial leader. •Working in the capacity of conducting the day to day activities of managing trials in various phases either with the understanding of the differences between clinical devel...
Currently we have an opening for QC Production Inspector to support a company located in the Paterson, NJ area. Responsibilities: Moistures Analysis, record, report. Auditing/inspection/hold/disposition of incoming ingredients, in-process & finished products; record, report. Packaging line control includes Metal Detection, Weight Control, Label Verification, etc. Production /special customers...
Company Confidential
Specialty coating manufacturer in Northern NJ has an opening for an Entry Level position that providestechnical documentation support to external customers and internal departments: R&D, QC, Marketing,Sales, and Customer Service. Responsibilities: - Research and understand domestic and global regulations in Cosmetics / Personal Care and keep up to date with changes that are made with these regul...
Company Confidential
Specialty coatings manufacturer in Northern NJ is seeking a professional, creative and productive color developer. Candidate must have experience color matching paints, lacquers, enamels or waterborne coatings. Color matching experience in the cosmetic industry is ideal. Main responsibility is to formulate products to satisfy customers’ requirements. Responsibilities: · Color match provided samp...