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ASSOCIATE CLINICAL SCIENTIST REQUIREMENT #16-00173 RECRUITER: MEGAN STRAWN JOB LOCATION: HOPEWELL, NJ JANUARY 28, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: We are seeking a Research Scientist with knowledge and background in molecular biology to develop, validate and test molecular assays in clinical trial samples. Members of the Clinical Mole...
PBMC SCIENTIST REQUIREMENT #16-00172 RECRUITER: JESSICA CLARK JOB LOCATION: HOPEWELL, NJ JANUARY 28, 2016 Project Description: We are seeking a scientist to fill an open position in the PBMC production group within biomarker technologies. The primary focus of this team will be processing high quality PBMC samples from whole blood of patients on various clinical trials for downstream flow cyt...
The Clinical Project Manager (CPM) will work in a matrix management environment and serves as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for spon...
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) Primary Responsibilities: Work with applicable stakeholders to develop understanding of the business need to be addressed by the analysis Uti...
Performs chemical, microscopic, bacteriologic and other medical laboratory tests and examinations. Operates manual and automated lab equipment for analysis of specimens. Shift is 12noon to 10p/rotating weekends. Required: ASCP Certification; at least 1 year experience as ASCP lab tech. COMPENSATION Base Salary - $47,800 to $65,500 Benefits - Full Relocation Assistance Available - Yes Commi...
Performs laboratory technical tasks. Responsible for the care and maintenance of laboratory equipment. Will be required to offer assistance in the operation of the equipment and the gathering of data. Assists with receipt and inspection of raw materials, ordering and stocking. . Requires an Associate's Degree or its equivalent and 2-5 years of related experience. Has knowledge of commonly-used con...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Biostatistician Apply Washington, DC Full-Time $65,000 - $110,000 Job Details Located in the DC area, we are the largest healthcare organization in the region! For over 4 decades we have conducted high quality translational and health sciences research and are currently in need of a Biostatistician to join ...
Job Description: CLINICAL RESEARCH COORDINATOR ? Opportunity To Develop Materials And Tools Necessary to perform the clinical study ? Opportunity To Collaborate With Study Investigator ? Opportunity To Serve As A Resource Person To Participants, Investigators, and Staff There is an IMMEDIATE need for a CLINICAL RESEARCH COORDINATOR who is seeking an opportunity to develop materials and tools ...
Position Title: Environmental Health Specialist Reports To: Director of Environmental Health Status: Non- Exempt (Fulltime 35hrs base workweek with benefits) Hours: 8:00am to 4:00pm Monday- Friday (some nights and weekends) Position Summary: The purpose of this classification is to perform specialized work functions to prevent the transmission of disease through the environment. This is accom...
Morgan Schaffer is a pioneer in Dissolved Gas Analysis (DGA). 2015 was our 50th anniversary and we are proud of our continued excellence across all or our lines of business. Our laboratory division includes operations in Montréal, Canada, as well as Philadelphia, USA. We specialize in the analyst of dielectric fluids. Using the higest quality processes and analytical instruments, we offer a full r...
Job Summary A Principal Clinical Research Associate has an important task within the clinical trial process. The position is responsible for verifying that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents. Most importantly, this position makes sure that the conduct of the trial is in compliance ...
Job Summary A Clinical Research Associate has an important task within the clinical trial process. The position is responsible for verifying that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents. Most importantly, this position makes sure that the conduct of the trial is in compliance with the c...
Seeking a person experienced in both environmental water and waste laboratory analyses. Are you interested? Please contact Bruce Rowles at ***** or call at 614.223.2316. Some of the tests performed are: ortho-phosphate, total Kjeldahl nitrogen, nitrate, nitrite, ammonia, dissolved oxygen, pH, temperature, turbidity, chloride, hardness, alkalinity, conductivity, sulfate, fluori...
Summary: The Senior Clinical Research Associate (Sr CRA) participates in the conduct of single and multi-center clinical research studies, presents at monitor training meetings and investigator meetings, monitors recruitment and overall study progress, addresses issues as they arise within the realm of the Sr. CRA position, and makes decisions with the guidance of the Clinical Research Manager (C...
The candidate should have a MS/PhD degree in biological sciences with experince in in Pharmacology and/or immunology and relevant work experience ( a minimum 5 years with MS degree, or 2-3 yrs with a PhD) in drug discovery research. The individual will be actively involved in planning and executing pharmacology studies involving both in vivo work in vivarium and in vitro/ex vivo laboratory work. ...
Type of Role: This is a professional individual contributor role that provides oversight and accountability for more than one low to moderate complexity trial or one high complexity trial. May be a member of more than one project of low to moderate complexity or member of one project of high complexity. Impact of Decision-Making: This position makes recommendations and influences decisions for s...
I. ROLE SUMMARY: Responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of quality studies, including in process quality control activities. II. PRIMARY JOB RESPONSIBILITIES: Primary responsibilities of this position include: Supports the Clinical Trial Management/operational study teams in the exe...
The Microbiology Analyst is responsible for performing microbiological tests that support the release of intermediates and finished products. These include routine and non-routine microbiological tests on in-process and final container products, as well as environmental monitoring samples. This position also contributes to the completion of routine technical tasks. Responsible for overall executi...
Description/Comment Reports Entering of data Sample tracking Sample scheduling and coordination Data copying Technical writing Stability set down activities Good client communication Flexibility Self -motivated Good attention to detail Good computer skills including excel, word, databases, Easily trained. LIMS knowledge desired Good knowledge of analytical methods types Analytical ...
Manager Praluent GHEOR Lead Job description Support large volume of activities in the PCSK9 Global Health Economics & Outcomes Research (GHEOR) department for alirocumab. Overall the position will support the GHEOR Leads to ensure successful planning and implementation of Global MA strategies in preparation for launch. Define and discuss the operational requirements within Global VE & MA and be...