R & D Jobs in Summit, New Jersey

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

Jobs 1 to 20 of 248
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...
Qualifications: Minimum of a BS degree Regulatory experience preferred Pharmaceutical/Biological manufacturing or Quality experience preferred Experience preparing CMC (Chemistry, Manufacturing, Controls) post approval submissions preferred Experience with Trackwise and regulatory tracking databases preferred Proactive and highly productive Sound judgment Attention to detail Strong written and ver...
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...
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, Review docu...
The Principle SAS Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, listings, figures, and tables) for major, complex clinical projects, acts as a technical expert to offer consulting, training, mentoring for programmers within the group, and may act as a programmer representative on major initiatives. Responsible for the integrity of the programm...
Responsibilities: This individual will be responsible for the collection of data from the LIMS and clinical data set, aligning/merging data sets, apply binding codes, and prepare merged data sets for pharmacokinetic analysis. Generate tables accounting for the disposition of patients and samples, descriptive statistics of pharmacokinetic variables, and results. Generate figures to include but not...
Company Confidential Summit, NJ, 07901
We are seeking a research scientist with proven success at the bench. Possesses a strong understanding of science behind ongoing experiments: the rationale, purpose and appropriate analytical methods. The position holder works virtually independently toward defined objectives conducting several complex experiments, some in parallel, and offering insight into future experiments. The scientist displ...
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 of...
A single owner for a specific offering (a set of tests, services and solutions) that could be defined around patient group/call point/clinical area. They coordinate development, deployment and post marketing surveillance of the offering, and generally ensure an integrated marketing plan is in place to achieve their assigned goals. The product director also works to build the business case and secu...
East Hanover, 07936
Expert Clinical Manager 6 month, renewable contract w2 candidates only Duties Under the guidance of the CTH assist with writing of amendments and CSRs and provide feedback on the data management plan. Be a delegate for the CTH at internal study meetings. Report study progress and issues, lead trial level interactions with Oncology Clinical Development Operations and other relevant functions includ...
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 maintenan...
Laboratory technician in precious metal assay services laboratory with leader in the chemical industry. Responsibilities: Will be responsible for performing a variety of classical wet chemical and instrumental analyses. Responsible for the measurement of Loss on Ignition/Drying by instrumental methods. Should be familiar with the techniques of instrumental analysis, to include XRay Fluorescence (X...
Depending on the candidate’s experience level, this role could be filled as an Analyst up to an Associate Director level. Based on the experience level of the candidate the responsibilities for this role will adjust accordingly. PRIMARY DUTIES AND RESPONSIBILITIES: Team Management/Mentorship Contributes to refinement and development of team mission/vision Grows and develops Managed Markets colleag...
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 safety co...
Manage projects/engagements delivering sales, marketing and managed markets solutions. Familiarity with the application of analytics to sales and marketing problems such as: • Commercial model design, Sales Force Sizing, Territory Alignment, Sales Call Planning, Incentive Compensation. • Market segmentation, marketing program ROI, marketing mix optimization. • Managed markets pull through analysis...
Great opportunity to join a leading global medical technology organization. This position will collaborate with Divisional and International Regulatory staff to execute the company’s regulatory strategies that ensure successful approval of international product registrations and renewals. Job responsibilities: Interpret and handle regulatory issues across business units and geographic locations. P...
We currently have a 6 Months Contract opportunity for a Biostatistician with our direct client located in Berkeley Heights, NJ. Responsibilities will include, but are not limited to, the following: · Work under the direction of Medical Affairs Statistics Disease Lead · Actively provide statistical support to the Medical Affairs Department · Provide statistical support for publications, presentatio...
-The primary responsibility of this role, as Senior Scientific Medical Writer, is: Act as the medical writing expert responsible for the research, writing and editing of study level and submission level documents. The incumbent will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Responsibilities will include assuring quality and...
The primary responsibility of this role, as Senior Scientific Medical Writer, is: Act as the medical writing expert responsible for the research, writing and editing of study level and submission level documents. The incumbent will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Responsibilities will include assuring quality and t...
Hello, My name is Samantha and I represent The Fountain Group. We are a national staffing firm and are currently seeking an Associate Director for a prominent client of ours. This position is located in Whippany, NJ. Details for the positions are as follows: Job Description: Supports the Director and Deputy Directors of GMA-Oncology Publications and Communications in the execution of the tactical...

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