R & D Jobs

R & D Employment Information


R and D Industry Overview


Companies involved in research and development (R and D) employ scientists, but they also need to fill many other R and D jobs, including those for statisticians, data managers, regulatory specialists, QA managers and others who support those who make scientific breakthroughs, apply discoveries and bring new products to market.

An R and D career typically revolves around one of three activities: conducting basic research, applying research findings or developing new products. The vast majority of jobs in R and D are found in physics, engineering or life sciences. Only about 12 percent of R and D job opportunities are found in economics, sociology, anthropology and psychology.

R and D Job Market


Several factors will influence the number of R and D jobs going forward. In the biotechnology industry, pharmaceutical companies have a record number of products in the pipeline as they seek to replace revenue lost from expiring drug patents. That pressure will keep merger-and-acquisition activity high, Life Science Digest predicts.

In 2012, federal government spending on R and D will drop while industrial and academic spending will rise, R&D Magazine predicts. Defense industry R and D jobs could be influenced by a $2.5 billion spending cut in Defense Department-funded research, the magazine says.Between 2010 and 2020, R and D employment will be quite robust, the Bureau of Labor Statistics (BLS) forecasts. It predicts:

  • Medical scientist jobs will grow 36 percent.
  • Biochemist and biophysicist jobs will grow 31 percent.
  • Physicist jobs and astronomer jobs will grow 14 percent.
  • Statistician jobs will grow 14 percent.
  • Chemist and materials scientist jobs will grow 4 percent.


R and D Salaries


Scientist salaries are typically tied to the amount of education needed for the particular job, with the highest salaries going to those with advanced degrees.

The mean salary for all life sciences R and D jobs was $76,140, the BLS says.

Statisticians working in R and D earned mean salaries of $86,370 in 2011, the BLS says.

The median salary for a clinical data manager working in R and D is $66,800, according to online salary database PayScale.com. Regulatory specialists in R and D earned a median of $55,900 and regulatory affairs directors in R and D earned a median of $146,000, PayScale reports.

QA managers’ median salary was $89,500 in 2012, the American Society for Quality (ASQ) reports. Having ASQ certification may boost a quality manager’s salary by $10,000, the ASQ says.
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1000+ R & D jobs found on Monster.

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* If you are unable to apply following our standard procedures and need accommodation, please contact us at (310)222-3616. SALARY COMMENSURATE WITH EXPERIENCE Required Skills & Qualifications: HS Diploma or GED certificate. Associate or Bachelor’s degree in health related discipline is preferred. Two years of clinical research experience is desired. Must be familiar with good clinical practice, IC...
Company: Yoh Senior Epidemiologist needed for a contract opportunity with Yoh's client located in Bridgewater, NJ. What You'll Be Doing: - Perform data analysis and statistical modeling for epidemiological studies to address safety issues for marketed products and products in development. - Develop programming codes following the study plan - Perform data analysis and statistical modeling - Genera...
Company: Yoh Research Associate needed for a contract opportunity with Yoh's client located in South San Francisco, CA. The Big Picture - Top Skills You Should Possess: - This includes providing clinical veterinary care of laboratory animals, health monitoring and diagnostics, and training of scientists and staff. - The individual will also conduct post-approval monitoring of research activities a...
Job Description: Prominent global pharmaceutical company is seeking a Quality Reviewer I to work in Durham, NC. This is a five month contract assignment. Hours are M - F, 8am - 5pm. Pay is from $28 - $34.75/hour. Summary: The purpose of this position is to support Quality documentation review and approval in a pharmaceutical manufacturing environment. Primary responsibilities include: Electronic B...
Team Lead-RN Clinical Trials of Texas, Inc. (CTT) is currently seeking an experienced and motivated Team Lead-RN for our Internal Medicine Team. The primary focus of this role is to manage our staff and manage clinical pharmaceutical and device protocols conducted at CTT while following applicable federal regulations/ICH guidelines, medical ethics, HIPAA rules, GCPs, IRB requirements, CTT's SOPs,...
Harnish Group Inc., is the Caterpillar dealer with operations in Washington, Montana, Wyoming, North Dakota and Alaska. We are best known by our Member Companies: N C Machinery, N C the Cat Rental Store, N C Power Systems and Tractor & Equipment Co. We take great pride in helping our customers succeed by providing premier solutions delivered by engaged employees through teamwork and excellence. Th...
Bench Reactor Chemist/Technician for an energy/utility company located in Charlotte. The Bench Reactor Chemist/Technician will be responsible for operations of the Bench Catalyst Test Reactor. This includes preparation of catalyst samples for testing, maintaining system operating conditions, performing various maintenance tasks associated with the test system, and preparing final test reports. In...
Please note this is a 5 months contract position Skills: Microbiology experience, GxP Documentation, Excel Description The individual will perform research studies utilizing standard and modified methods in-vitro such as microbial kill time and minimum inhibitory concentration. Clinical studies will require cup-scrub sampling to collect facial skin bacterial samples from human subjects, processing...
· Test and document samples of raw materials, products in process, finished products, water, and other samples provided by various departments to help ensure quality in the manufacturing process. · Adheres to cGMP and other applicable regulations. · Perform USP Antibiotics - Microbial Assays · Perform USP (USP, ) limits testing on samples. · Perform USP andand EP 5.1.3 Antimicrobial Effectiveness...
General Description:This senior-level position will be significantly involved in research and development projects involving new nutritional supplement products, new product concepts and scientific initiatives. Important objectives include collaboration on an integrated strategy with implementation across the product development department. Must excel at working within a demanding, success-oriente...
BioCure is now looking for a Development Chemist with a strong academic background in biology, analytical chemistry and protocol development. This position will grow internally at BioCure within the Product Development, Quality Systems Design Control or Advanced Research groups. BioCure develops proprietary hydrogel and polymer tri-block technologies for use throughout the human body or in diagnos...
Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi...
Senior Medical Writer - Biotech Company seeks a Senior Medical Writer to prepare clinical documents under strict timelines to support drug development at their Bridgewater, NJ facility. This is a full-time position, where you will earn a highly competitive salary, based upon your experience. You will also receive a full benefits package and the potential to earn a discretionary annual bonus for ex...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply R&D Scientist - Data Mining / Modeling Business Analysis Newark, DE Full-Time $90,000 - $120,000 Apply Apply R&D Scientist - Data Mining / Modeling Business Analysis Newark, DE Full-Time $90,000 - $120,000 Apply Job Details R&D Scientist - Data Mining / Modeling Business Analysis *We will relocate the right f...
THE POSITION The Manager, Regulatory Strategy will be responsible for registration and regulatory support of US commercial and development projects. This position may be located in either Palo Alto, CA or Philadelphia, PA. RESPONSIBILITIES Participate as an active member of a multi-disciplinary team to establish development and regulatory strategies for commercial products, late stage, and early s...
Our client is a well-established pharmaceutical company seeking an experienced Scheduler/Planner with a proven record in planning virtual supply chains. You will have the opportunity to serve as a key contributor within this vibrant Supply Chain team. The primary responsibilities for this position include: · Converting figures from Global Commercial forecasts, Global Clinical Demand Forecast and i...
Purpose Performs special projects and monitors the pharmacovigilance (PV) system to ensure patient safety, full regulatory compliance and timely flow of drug safety information to clinical teams and senior management. Acts as a liaison internally and with external collaborators to administer programs and processes to meet global regulatory reporting requirements Essential Functions Meets with mana...
Lab Support has a great Direct Hire opportunity for a Research Chemist who will be responsible for managing studies to include writing study protocols, supervision of personnel, project organization, communication of data/results to clients, writing study reports and compliance with protocols, SOP’s, and GLP regulations. • At least a B.S. in Chemistry (emphasis in organic chemistry) and 5-10 years...
You're precision-oriented, intuitive and a stickler for doing it right. You're a critical thinker who is adept at using logic and reasoning to identify the strengths and weaknesses of alternative solutions. You understand the value of working as a team, yet you function strongly on your own. If this describes you, you'll want to learn more about this opportunity from Experis. As a Document Control...
Job Title: Senior Clinical Quality Assurance Consultant Major Objectives: This position is responsible for management and continuous improvement of the GCP Quality System in compliance with regulations so that the quality of the company’s products is maintained, the patients’ interests are protected and client quality objectives are met. Also, to ensure that outsourced third parties are inspection...
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