R & D Jobs in Summit, New Jersey

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194 Summit, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 194
Currently we have a temporary opening for a Facilities Engineer to support a company located in the Short Hills, NJ area.   Responsibilities: Manage major construction projects at multiple North American sites. Developing design concepts with the users and design engineering firm Developing request for proposals to bid projects, coordination with customers, contractors and consultants, Revie...
Support study data management and data cleaning process on an ongoing basis, applying study specific documents and conventions. Identify and issue queries, incorporate query replies, track query status and apply permissible clarifications using the EDC (e.g., RAVE) and related systems (e.g., SAS, jReview, etc.). Assist in documentation gathering and archiving. Minimum 3 years as a Study Data Mang...
Job ID: 4294 Position Description: Company Overview At EngageCE, a division of PDI, Inc., we believe instilling positive behavior within the practice is the cornerstone of providing optimal patient care. Many practices face challenges and old habits that impact their ability to follow care recommendations, which can negatively impact patient outcomes due to: • Difficulty establishing and maint...
Outstanding CDM opportunity available with a growing clinical research organization in the Northern New Jersey area. A positive work environment and recognition of the importance of work life balance has led to employee satisfaction and company success. A competitive salary and comprehensive benefits package are offered. Job responsibilities: The Sr. / Clinical Data Manager leads data management...
Clinical and Regulatory Analyst - III Must have: - Bachelor's degree, preferably in nursing, pharmacy or a biological science - At least three years of experience in a hospital, pharmaceutical, or research position. - Prior experience in coordinating and overseeing the production of Aggregate Reports (PSUR, DSUR, PAER etc.) and RMPs required. - PSUR authoring experience would be considered. ...
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...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
PRINCIPLE ACCOUNTABILITIES · To support clinical trials at assigned sites including the responsibility of site management by coordinating all activities pertaining to qualification and initiation of and ongoing site support for the clinical trial. · To provide in-service education and training for physicians, hospital personnel and office staff on study related documents and devices in support o...
This position is to cover for a manager who works on 1 compound for the CD&MA Hematology team. This manager is currently the lead for the program and has 2-3 direct reports. Manage launch preparation activities, start-up and planning of a Novartis sponsored study, and coordinate an extensive third party study program. The individual will oversee the entire US clinical program for this compound. ...
Are you looking for a Clinical Research position with a large pharmaceutical company? TechData Service has multiple positions open with many top pharmaceutical companies for positions including Project Manager with quality systems experience, Drug Safety Coordinator, Pharmacovigilence Scientist, Clinical Operations Manager/Project Manager, Scientist, Medical Information Specialist, CRA Monitor, C...
Company: Yoh Clinical Reporting Consultant (Sunshine Act) needed for a contract opportunity with Yoh's client located in East Hanover, NJ. What You Need to Bring to the Table: - A cross functional team of subject matter experts ( SMEs) are collecting, validating, and reporting Clinical research related spend data and transfers of value for Sunshine transparency reporting. - The contractor will...
Company: Yoh Clinical Research Associate needed for a contract opportunity with Yoh's client located in East Hanover, NJ. What You'll Be Doing: - Responsible for implementation of operational aspects of clinical development and medical affairs trials in the US Hematology franchise. - Interfacing with the oncology therapeutic area global and U.S. clinical team members to conduct trials in maint...
TechData is looking for Biostatistician, Outcome Research Biostatistician,SAS Programmer/Statistical Programmer (Some can be telecommuting), Translational Operation Manager, Outsourcing Manager, Drug Safety Specialist/Trial Safety Manager, Clinical Study Manager/Clinical Research Scientist, Sr. Clinical Data Manager for our pharmaceutical clients in Central NJ and Northern NJ. Please see below req...
Manager, Trials Safety Surveillance • To provide excellent safety support to Development and Marketed product studies • To assist medical affairs teams and the lead safety MD in identifying and managing safety concerns • To ensure effective safety surveillance across trials • To draft safety sections of key trial documents Responsible for: • Identifying and assisting in the management of saf...
Great opportunity to join a leading, global medical device technology firm. This position will collaborate with Divisional and Global Regulatory staff to execute the company’s regulatory strategies ensuring successful approval of international product registrations and renewals. Primary Job responsibilities: · Effectively deal with regulatory issues across business units and geographic location...
Leading pharma clients seeks a Regulatory CMC Associate for a 6 month contract. Successful candidate provides strategic and operational global CMC regulatory direction and documentation for MARKETED PRODUCT maintenance. The following activities may be performed within this capacity: Provide and/or implement global CMC regulatory strategy for products. Lead or contribute to global CMC submissio...
Pharma client seeks a Pharmaceutical Quality Systems Project Manager for a 6 month contract with possibility of extension. ***Travel to local sites required*** Quality Systems Duties: - Perform project management functions for transfer of Quality Systems for site to site transfer: FARs, Deviations, CAPA, Change control, Documentation, Training systems, Complaints, Release, etc. - Lead activitie...
GPV Alliance Management Contractor Requirements: -Bachelor’s degree in the legal field, at least 2 years of relevant work experience contract drafting and negotiations and experience working with contract databases. -The ideal candidate will also have experience working in the pharmaceutical industry environment and will have knowledge of global pharmacovigilance regulations and concepts. -Exc...
Requirements: -MD with 5+ years of pharmaceutical experience; specializing in cardiovascular, pulmonary or critical care medicine. -Expertise in Nephrology. Responsibilities: -Individual will support US medical affairs focusing on phase 4 development program and support of technical information regarding cardiopulmonary products. Location: Whippany NJ Duration: 10-20 hours per week for perio...
In more than 85% of America households, consumers reach for Pinnacle Foods brands. Pinnacle Foods is a Top 1000 Company as ranked by Fortune Magazine. We are a leading producer, marketer and distributor of high-quality branded food products, which have been trusted household names for decades. Headquartered in Parsippany, NJ, our business employs an average of 4,400 employees. We are a leader in t...

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