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R & D Jobs in Elizabeth, New Jersey

463 jobs

Must have: - M.D. - Independent Clinical Monitoring Experience - at least 3 years of experience in drug development required, including experience in medical monitoring, and in writing of protocols and study reports; experience in authoring sections of filing documents is desired. - Demonstrated medical knowledge, strong scientific analytic skills, and strong writing skills required. - Experi...

Requirements: -A Bachelor’s Degree in Life Sciences or Engineering discipline; Advanced degree preferred -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 through the various phases of product development is required -Experienc...

Hatch Mott MacDonald (HMM) is an award-winning consulting engineering firm with major success in the fields of architectural services; highway and bridges; aviation; rail and transit; water and water resources; wastewater; environment; municipal engineering; ports and harbors; tunnels; and pipeline services. We have earned a reputation for technical excellence on some of the world's most prominent...

ADMINISTRATIVE ASSISTANT MUST HAVE PHARMACEUTICAL INDUSTRY EXPERIENCE REQUIREMENT #15-01152 RECRUITER: ANITA JORDAN JOB LOCATION: JERSEY CITY, NJ AUGUST 13, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The increase to both size and scope of the MCCM group has led to a need for incremental administrative support in order to provide for the increase...

Job Description: Prominent global pharmaceutical company is seeking a Manager, Clinical and CMC Planning to work in Jersey City, NJ. This is a six (06) month contract assignment with the possibility of extension/ temp-to-hire. Max pay is $51.50/hour. Summary: The Manager, Clinical and CMC Planning is responsible for supporting Clinical Trial/Project Teams by strategically developing and maint...

Our client is seeking an ASR Senior Specialist. They are seeking candidates with safety/pharmacovigilance experience coupled with a project management background. The ideal candidate should have document management experience and strong communication skills in order to help facilitate the aggregate report production activities. This person will also be responsible for maintaining project schedule...

Summary: Performs complex testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records. Minimum Qualifications: Bachelors degree in Chemistry or related science from an accredited college or university and a minimum of two (2) four (4) years of related laboratory work experience; or two...

Regulatory Affairs Associate Requirements: -BS or MS degree in a scientific field such as Pharmacy, Chemistry, Biology, etc. -2 years in Regulatory Affairs, in generic Pharmaceutical Industry, or 2-4 years’ exposure in Pharmaceutical field such as Analytical, Products Development or Manufacturing Responsibilities: - Preparation of ANDAs, Supplements, Annual Reports and responses to FDA review...

Refinery in North-East New Jersey has two Control System Engineering openings. One position is a Controls System Engineer and the other is a Controls System Project Engineer. Both require extensive experience in a refinery/chemical environment, extensive controls systems (DCS & PLC) knowledge/experience & the Project Engineer should have experience leading controls system projects in a refinery/ch...

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...

Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $1.5 billion in annual revenues and 17,000 employees across 200 sites in 36 countries, Eurofins is a leading internation...

Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating over 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized labor...

As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to evacuate the area, control the situation, and solve the problem. In order to perform these functions, you will be trained to e...

Title: Associate Director, Clinical Research Knowledge of Women s health and Urology therapeutic experience Preferred. Must have Clinical Development experience in the pharmaceutical sector. Serve as a Clinical Lead at the study level and as the single point of accountability for clinical strategy, design, review, clinical oversight, and reporting of a clinical study or group of studies within ...

Manager, Feasibility Analytics for Clinical Trials Requirements: - Bachelor’s degree in life science or equivalent field -Minimum of five years relevant clinical research experience in a pharmaceutical company/CRO -Ability to review/analyze relevant data so as to build evidence-based clinical trial strategies -Ability to design/develop effective strategies to bring about trial success, as def...

Manager, Global Drug Safety Requirements: -BS in Nursing or Pharmacy or PharmD preferred -Knowledge of FDA, EU, and ICH guidelines and regulations -Knowledge of Pharmacovigilance and Risk Management -Knowledge of Coding dictionaries (e.g., WHO ATC drug dictionary, and MedDRA) -Drug safety database knowledge: ARISg, Argus, Business Objects (reporting tool) and Empirica (data mining software t...

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. Description Overall steering of a selected R&D project port...

ASSOCIATE CHEMIST - ASSOCIATE CHEMIST - ASSOCIATE CHEMIST The Analytics and Materials Characterization group in Iselin NJ is part of the Catalyst Research and Development department of the company. We provide fundamental understanding and problem solving to the company's environmental, refining and catalyst manufacture businesses. The successful candidate will be responsible for sample preparat...

SAFETY INFORMATION COORDINATOR REQUIREMENT #15-01137 RECRUITER: CINDI PISNOY JOB LOCATION: JERSEY CITY, NJ AUGUST 11, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The Safety Information Coordinator receives all non-telephonic incoming safety information, evaluates, compiles and qualifies the information for completeness, confirms receipt with Asso...

ASSOCIATE DIRECTOR, CLINICAL RESEARCH REQUIREMENT #15-01096 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ AUGUST 4, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Serve as a Clinical Lead at the study level and as the single point of accountability for clinical strategy, design, review, clinical oversight, and reporting of a clinical study or...