R & D Jobs in Dover, New Jersey

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98 Dover, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 98
Our client in Morris Plains, NJ is looking for a Drug Safety Coordinator I . This is a long term consulting position. If interested, Please apply to this ad Job Title: Drug Safety Coordinator I Job Location: Morris Plains, NJ Job#: 14-01431 Job Description: Responsible for the receipt and data entry of adverse event reports following company standard operating procedures, internal business practic...
Great opportunity for Senior to Lead SAS Programmers. Competitive, salary, benefits package, and bonus available. Responsibilities include: •Acts as the lead programmer on multiple studies •Manages project timelines, budgets, and resources •Effectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budget •Oversees the programming a...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Chief Medical Officer Morris Plains, NJ Unspecified Apply Apply Chief Medical Officer Morris Plains, NJ Unspecified Apply Job Details If you are a Chief Medical Officer with experience, please read on! We are committed to be a leading, innovative bio-pharmaceutical company, dedicated to improving patient's he...
POSITION: Subsurface Evaluator LOCATION: Sparta, NJ OVERVIEW: An innovative environmental testing & technology company is currently seeking aNJDEP licensed Subsurface Evaluator for our Sparta, New Jersey office. The company needs an energetic and experienced Subsurface Evaluator who is available to start a new opportunity. If you are a team player with strong quantitative skills, an environmental...
Outstanding opportunity for a leading pharmaceutical and OTC organization. This is a full time position offering a competitive salary and benefits. The position will be based in the White Plains, NY area. Relocation assistance provided. Job Information: · Develop and review of clinical protocols; review of scientific literature; and work with physicians and external consultants to develop clinical...
Exciting opportunity to join a select team that is leading the way in the Pharmaceutical/Biotech industry.Competitive salary, bonus incentive program and comprehensive benefits package offered. The position will serve as a subject matter resource for identified area(s), including relevant activities in assigned Therapeutic Area program(s) or Business Objects program. Job Responsibilities: · Work w...
Job Number: 422326 Clinical Research Manager QUALIFICATION REQUIREMENTS: A minimum of a bachelor's degree is required. Advanced degree preferred. Must have an in depth understanding of the drug development process as well as the operational and regulatory aspects of clinical development. Understanding if ICH GCP guidelines and sponsor responsibilities. A minimum of 7 years of study management expe...
Qualified candidates will have 5 years of Medical Information experience: Writes and updates relevant, unbiased custom and standard response documents and product profiles for products to ensure information provided to customers represents the most complete and accurate information. Acts as expert in therapeutic areas of responsibility and uses this expertise to influence appropriate decision maki...
Must have: -Must have a degree in Pharmacy (PharmD preferred) -2 years of experience in corporate medical communications and/or medical information experience Knowledge of: -Food and Drug Administration (FDA), and other regulatory requirements. -Pharmaceutical principles, practices and their application. -Medical terminology and treatment modalities. -Pharmacology principles, theory and their appl...
Requirements: -Associate's degree in Healthcare or business related field from an accredited college or university, and a minimum of one (1) year directly related experience; or, an equivalent combination of education and/or experience. -Experience with Food and Drug Administration (FDA), and other regulatory requirements. -Customer service procedures and techniques. -Computer systems and database...
Our client is a growing CRO offering an outstanding opportunity to join their organization and play an integral part of their departmental growth. This position provides leadership and guidance as the statistical expert to ensure projects are optimally strategized, correctly designed, properly analyzed and clearly presented to support new product development, domestic and international regulatory...
Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: NJ - Flanders Req ID: 135549 Position Title: LABORATORY TECH 3 Experience Level: Not Indicated Education Required: Bachelors Degree or equivalent experience Travel Required: No Company Description: Siemens’ Healthcare Sector is one of the world's largest suppliers to the healthcare industry and a leader in medical...
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...
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. -Excellent communication and English langua...
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. -Excelle...
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 period of 3...
Requirements: -MS, PhD or Pharm D required -6-9 years related experience within biotech/healthcare industry Responsibilities: -Supports the Director and Deputy Directors of Oncology Publications and Communications in the execution of the tactical publications plans for assigned oncology products, to ensure the timely presentation of data at key Congresses and rapid journal publication. -Reviews an...
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...
COMPANY: This Company is a global enterprise with core competencies in the fields of health care, nutrition and high-tech materials. Their products and services are designed to benefit people and improve their quality of life. At the same time they want to create value through innovation, growth and high earning power. LOCATION: Whippany, NJ DESCRIPTION: The primary responsibility of this role, as...
. A Clinical Data Manager job is available in Northern NJ courtesy of Adecco Engineering and Technical. You will need to support the execution of data management activities necessary for the preparation of submission data and required documentation for regulatory authorities. You will be the primary contact for Global Data Management on the Core Study Team. The Clinical Data Manager responsibiliti...

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