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R & D Jobs in Trenton, New Jersey

255 jobs

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...
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: ...
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...
Since its’ founding more than 20 years ago, QPharma has been at the forefront of regulatory compliance and brand support for the pharmaceutical, medical device, and other life sciences industries. Our team of consultants, project managers, and subject matter experts possesses the extensive knowledge, access to resources, and key regulatory contacts necessary to excel in the execution of any proje...
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 ...
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...
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...
Position: - Clinical Site Manager (Central Lab Set-up Specialist) Duration: - 6 months Location: - Lawrenceville, NJ,08648 Job Description: Monitor progress of assigned investigator countries/sites through close contact with site staff and monitors. Disseminate appropriate site related info to involved client team members. Key contact for protocol-related issues. This position supports the ...
Responsibilities: Excellent employment opportunity for an Epidemiology in the Titusville, NJ area. The Epidemiology will provide direct and independent programming support for the implementation of claims or electronic medical record (EMR) database studies; and conduct quality assurance review of other programmer’s codes and analytic files. Experience: To be considered for this Epidemiology jo...
Our client, a Global Beauty Company in Bristol, PA is currently seeking an experienced Microbiologist to join their dynamic QA team! This role is ideal for someone with 8+ years of Microbiology experience in cosmetics/pharma or a related field. This is an immediate need so please apply if your are availability immediately. Summary: Support laboratory operations to ensure that all Filled Products...
Chemist Langhorne, PA Clinsmart LLC, a contract research organization located in Langhorne, PA offering comprehensive clinical development services to the pharmaceutical, biotechnology and medical device industries, seeks qualified individual to develop and formulate various dosage forms and review the chemistry and manufacturing controls of drug regulatory applications and submissions, includin...
A large pharmaceutical company in New Jersey that is seeking to hire a Senior Scientist and a Principal Scientist for their downstream process development group. They are offering full relocation as well as a competitive compensation package. This company has over 20 years of process development experience and has more than 240 biologic development programs. This role requires the following quali...
I am currently partnered with a rapidly growing organization to help them find a Senior Clinical Data Manager. The position is with a small CRO focused solely in oncology. Over the last 30 years, this organization has made a name for themselves as the go-to CRO for highly complex oncology studies. This is an opportunity as a Senior Clinical Data Manager to be a big fish in a small pond. The Senio...