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R & D Jobs in Irvington, New Jersey

621 jobs

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...
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...
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: 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...
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...
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 ...
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...
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...
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...
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...