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R & D Jobs in Lawrenceville, New Jersey

350 jobs

Position Summary: This role is responsible for supporting and coordinating the development and execution of the strategic publication plans under the management of the Director, Medical Communications. In this capacity, the Associate Director will oversee day-to-day management of the publication plan and will be responsible and accountable for all aspects of the publication development timelines ...
Growing pharma client with an extensive portfolio of approved and investigational products in cardiovascular therapies and a significant pain treatment franchise is seeking a Director/Sr. Director Regulatory Affairs. ****This role is the point person for the FDA and reports directly to the CMO. The Director/Sr Director of Regulatory Affairs provides regulatory expertise and support for commercia...
Job Number: 439962 Manager, Medical Writing OVERVIEW: Essential Skills Needed for Assignment: Provide support for MWs by preparing a variety of non-data dependent sections for approved template documents from other source documents Oversee and coordinate the creation, compilation, and finalization of clinical study report (CSR) appendices. Maintain and update trackers for all CSRs (other pro...
Duties & Responsibilities Line/personnel management: Manage and direct the efforts of CRAs assigned to project. Manage performance, scheduling and work assignments Define and communicate job descriptions, core competencies, performance standards and expectations Coordinate regular meetings (at least the frequency of two meetings a month) Establish accurate and consistent productivity expectat...
Bioclinica, Inc. is looking for intelligent, creative and dedicated professionals to join our growing team. We are a company that values technical excellence, teamwork and a commitment to success. We employ cutting edge technology to provide our customers with industry leading solutions and are currently seeking to fill the position of Global Manager, Site Services to work out of our Princeton, NJ...
Provide support for MWs by preparing a variety of non-data dependent sections for approved template documents from other source documents Oversee and coordinate the creation, compilation, and finalization of clinical study report (CSR) appendices. Maintain and update trackers for all CSRs (other projects as needed). Contact appropriate departments to keep tracker on timeline target (knowledge of...
Job Description: This position is responsible for the management and delivery of regulatory submissions required to support the development, registration, and compliance of products. Depending on the particular project and assigned submission(s), required activities may include, but not be limited to: Establishing Dossier Plans for the assigned submission types / projects considering inputs from...
Position: Regulatory Affairs Manager II Duration: 05 Months Contract Location: Titusville NJ 08560 Summary: · This position is responsible for the management and delivery of regulatory submissions required to support the development, registration, and compliance of products. Depending on the particular project and assigned submission(s), required activities may include, but not be limited to: ...
Seeking a Sensory Panel Leader for a long-term consulting position at a pharmaceutical client in Skillman, NJ 08558. *** Entry Level Biology or Chemistry graduates with wet lab experience are OK *** Overview: Supports the Sensory Category Lead and the Sensory Program Lead in the execution and support of sensory studies, panelist reviews / training sessions, and other Sensory Program initiatives ...
ENGINEER/GEOLOGIST/ENVIRONMENTAL SCIENTIST – Entry Level A full servicefirm offering innovative solutions to a broad range of engineering, health & safety, and environmental issues seeks a motivated Environmental Professional for work out of our Robbinsville, New Jersey office. Candidates should possess: An Associate’s or Bachelor’s degree in Environmental Engineering, Geology, Environmental Sc...
Growing medical digital technology and communications company headquartered in central New Jersey is seeking two highly qualified professionals to join our organization. Our company specializes in the development of promotional and educational programs and tools for the pharmaceutical industry. We integrate digital technology expertise and high-science content to achieve innovative solutions. DIG...
Our client is currently seeking a Analytical Scientist. Description The Analytical Scientist will be involved in the design, planning, organization and evaluation of drug product and combination drug/device product development. They will perform analytical testing on inhalation devices (aerosol performance testing) as part of the aerosol team within Analytical Chemistry. The position requires use...
Our client, a prestigious cosmetics company in Melville, is looking for a recent college graduate! They are hiring for a Package Testing Associate to work in their logistics department. The primary responsibility of this position is the procurement, evaluation, and testing of packaging components and materials. Job Responsibilities include: Works closely with suppliers and developers on the proc...
QC Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Knowledge in cGMP, GLP, and compendia procedures (FCC, USP-NF) BS in Science Minimum 1-2 years of similar work experience Solid Dosage/ wet chemistry Minimum of 2 years’ experience in raw material and finished product analysis by Wet Chemistry, Potentiometric & Karl Fi...
About the Job Office Based in Central, N.J. , Our Client, a major medical devices company (a subsidiary of a major pharmaceutical and healthcare products company) is seeking several experienced research professionals for its medical devices group. The position is responsible for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clini...
Amec Foster Wheeler (www.amecfw.com) designs, delivers and maintains strategic and complex assets for its customers across the global energy and related sectors. With pro-forma 2014 annualized scope revenues of £5.5 billion and over 40,000 people in more than 55 countries, the company operates across the whole of the oil and gas industry – from production through to refining, processing and distr...
About Spice Chain Corporation: The Company is a customer centric, diverse, energetic and rapidly growing supplier, processor and packager of spices and seasonings, based in New Jersey. SUMMARY Research & Development for Spice Chain Corporation is responsible for ensuring customer samples (from production and developed) are created and tracked accordingly. This position supports the head of resea...
Requirements: RN 3+ years of experience in ICU, ER, home health/oncology nursing experience Prior experience with patient populations with diabetes, COPD, HIV/AIDs, hypertension, Parkinson’s, RLS, Stroke, Venous Thromboembolism Description: Taking inbound calls in from Doctors, Nurses, and consumers for a specific pharmaceutical program in a call center environment Answering medical inquirie...
We have an immediate position for a “Regulatory Affairs Manager” with our top pharmaceutical client, if you are interested please send your updated resume to chris @ collabinfo.com or call me at 732-788-3483. Title: Regulatory Affairs Manager Duration: 12+ Months Location: Raritan, NJ Job Description The RSI Manager provides regional strategic implementation support for projects Immunology Th...
Sunrise System Inc. is currently seekingClinical Research Project Manager in Raritan NJ for one of our top clients. Title:Clinical Research Project Manager Location: Raritan NJ Type: Contract W2 only Duration: 12+ months ID # 16-09642 Job Description Development and execution of JGS funded market access deliverables (payer advisory boards, consulting, global value dossiers, research projects...