R & D Jobs in Lawrenceville, New Jersey

136 jobs

PHARMACIST POSITION @ RISOLDI’S PHARMACY DEPT. MERCERVILLE, NJ 08619 DUTIES & RESPONSIBILITIES: All duties include NJ licensed registered pharmacist. NATURE OF WORK: Duration: Full time, Part time Working hours: 40 per week POST IS OPEN TILL: JUN 25TH 2015 EDUCATION: Applicants should have a PHARM-D Degree. RESPONSE VIA E-MAIL (only): *****...

Job Requisition Number:46253 The Role: Bloomberg Intelligence (formerly known as Bloomberg Industries) provides a comprehensive view of an industry and its key constituents and, combined with the power of the Bloomberg Professionalr service, gives you unsurpassed depth and breadth at the sector, industry and company levels. Bloomberg Intelligence also offers valuable written analysis, industry d...

Job Number: 429593 Medical Writer Overview: Flexible attitude with respect to work assignments - willingness to work in a matrix environment Write/edit clinical documents for submission to regulatory authorities, including but not limited to: Statistical Analysis Plans, briefing documents, human pharmacology summaries, investigator brochures, study protocols, clinical study reports Serve as M...

The Study Manager will conduct and oversee all aspects of validation and sample analysis for various immunologic (ELISA, CBA, ECL) or Flow Cytometry projects. They are responsible for the overall conduct, budgets of assigned projects, ensuring regulatory compliance, and communication with all internal and external clients. Strategic *Maintain up to date knowledge of scientific advances, analytic...

“About Xcenda” Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex an...

About Xcenda Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and cost-...

About Xcenda Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and...

Theradex® is an international contract research organization with over 30 years of experience providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic tests in the areas of oncology and life-threatening diseases. Theradex® conducts clinical trials towards the goal of marketing approval for new agents with the pot...

inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Sr. Project Coordinator Location: Princeton, NJ (Office-Based) Job Description: · Set-up and maintain project files (electronic and hardcopy) · Set-up and maintain project plan · Maintain and distribute study-specific tracking reports · Support project meeting preparation, execution and collection/distribution...

Required Skills: Site Management Experience, Clinical Trial Experience, Clinical Monitoring Experience Please note that this is a 2-3 month contract. A Site Manager is the person in Trial Co-ordination and Site Management that serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through complianc...

Medical Information Therapeutic Manager Medical Information Therapeutic Manager Needed in Plainsboro, NJ !!! We are currently seeking a Medical Information Therapeutic Manager in the Plainsboro, NJ area with one of our direct client in the Pharmaceutical industry. If you or anyone you may know is available and interested, please apply now or simply forward this job posting. In addition, please r...

Job Description Packaging Engineer III (Princeton, NJ area)- Leading Global Consumer Products / Pharma company One of the world’s most respected and leading global Consumer Product/Pharma companies, located in Skillman, NJ (Princeton Area has an immediate need for an experienced Consumer Product Packaging Engineer: Preferred Experience: Skin Care, Cosmetics and Pharma; FDA / GMP experience pre...

Seeking a Quality Systems Lead for a consulting position at a pharmaceutical client in Skillman, NJ 08558. • A minimum of a Bachelors degree is required. A focused degree in a technical, scientific or related field is preferred. • A minimum of 10 years industry experience is required. • A minimum of 5 years of QA experience in the pharmaceutical or medical device industry is required. Regulato...

Quantex seeks an Office Manager/ Admin Assistant with solid accounting skills and knowledge of Quick Books Pro to provide administrative and book keeping support. The position reports to the Company’s CFO. Responsibilities include but are not limited to: produce general correspondence; create presentations and reports; maintain calendars and coordinate meetings and special events; schedule travel...

Experis Engineering has an immediate opening for a Lab Technician. This is a 12 month contract position. The Lab Technician will be assisting formulators in pharmaceutics with product development activities. This position is located in Cranbury, New Jersey. Local candidates are preferred. The Lab Technician will have the opportunity to: Set-up, disassemble and cleaning of processing equipment in...

Associate Director, Drug Safety Medical Evaluation, Drug Safety Physician -15-20% Domestic and international travel maybe required. Must work on site ¿ Provides medical review and evaluation of safety information and adverse event reports for both marketed and investigational medicinal products and medical devices. Performs scientific review and evaluation of individual and aggregate adverse eve...

Manger through Director level, CMC Regulatory Affairs positions available. Multiple PERM opportunities with reputable pharmaceutical companies throughout New Jersey and Maryland. CMC Regulatory Affairs (Manager/Director) will provide regulatory leadership and oversight to for both pre- and post-approval roles. Emphasis will be primarily on biologics products, so large molecule experience needed. ...

Senior Regulatory Affairs Requirements: Ph.D. or Pharm. D. preferred. Bachelors or Masters Degree in a scientific discipline or equivalent will be considered Regulatory Affairs Certification is favorable. Minimum of 8-10 years of regulatory experience respectively within the pharmaceutical or biotechnology industry Recent experience directing the preparation of eCTD NDA submissions Must have...

Quality Analyst (Laboratory Chemist) Cytosorbents, Inc. Cytosorbents, Inc. is a growing company in the Princeton, NJ area. We are seeking a Quality Analyst to join our team. This is a laboratory-based position that will be responsible for testing and analyzing raw materials and finished product. Responsibilities include: Conducts qualitative and quantitative assessments to monitor product and p...

Company Confidential
Aprecia Pharmaceuticals is hiring! Responsibilities: As a small start company employees are needed who are willing to perform any activity in their department and help support all other departments when needed. This position shall work in documentation and support cGMP compliance. As a member of the Quality Assurance team this position will oversee aspects of the Quality Assurance department rel...