101-120 of 189 results
Sort By


Our client is a fast-growing established world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative selling out client's line of microwave synthesis, extraction, and digestion instruments and will also include a line of Raman spectrometers. The territory includes ND, SD, NE, IA, MO, KS, MI, WI and MN. Candidates will ideally be located in Chicago, but other major cities in the territory will be considered. Qualifications:Must have a....

- San Fernando Valley, CA

Seeking a candidate to organize and coordinate new site recruitment as well as create and implement unique Pharma studies. The candidate will work closely with the Medical Director to select new sites to join our growing USA and International network as well as develop and implement original studies and help seek Pharma sponsorship. The candidate will maintain high levels of organizational effectiveness and communication. Our ideal candidate will be able to manage multiple sites for....


The Clinical Trial Data Analyst is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other sources. In addition, the position coordinates in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. Responsibilities: Prepare data reports, tables and graphs for regulatory submissions, IRB submissions,....


This position is responsible for leading internal and outsourced Clinical Data Management activities in support of Clinical Research studies, managing the definition of Case Report Form (CRF) requirements, creation of the Data Management Plan, coordination of Centralized Data Review activities (a key component of Risk-Based Monitoring), and is accountable for data integrity, quality, and consistency at Database Lock. The employee must be able to lead data review activities and engage different

- Lancaster, SC

Roles and Responsibilities:The R&D Chemist (RDC) reports to Quality Control (QC) Management. The R&D Chemist (RDC) work closely with Product Development and Quality Control. The RDC will be the Liaison between Quality control, Product Development, and Contract laboratories by evaluating and Assessing testing methodologies and their application to different sample matrix. This responsibility also includes the evaluation of testing results from contract laboratories to be sure that the....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Sales Representative for its industry leading analytical instrumentation used in R&D laboratories. This position will be covering Philadelphia and southern New Jersey. Responsibilities:The Technical Sales Representative will be responsible for direct sales of analytical instrumentation products and services (measuring density & viscosity) to R&D customers in various industries like....

- Sacramento, CA

Requirements:B.S. Engineering Degree, experienced non-degree acceptable5+ years’ of production floor supervision experiencePluses would be experience out of pharmaceuticals, foods or specialty chemicals and union experienceJob Description: Our client is an expanding player within the pharmaceutical industry. This person will work in a 400-person active pharmaceutical ingredients (API) manufacturing facility. This site runs on a 12-hour shift schedule and in this role, this person will....


We are looking for a Quality Assurance Specialist who will be responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QA Specialist will be readily available to support the Quality Department and the production process; therefore, this position requires the QA Specialist to be flexible based on business need to support QA and business....


Global Specialty Pharmaceutical company in Bridgewater, New Jersey is looking to hire a Manager of Clinical Quality AssuranceThe Manager Clinical Quality Assurance is a key member of the company Research and Development organization. This role is responsible for Clinical QA activity related to the planning, conduct, and reporting of GCP audits in order to ensure that clinical studies are conducted in compliance with applicable regulations, guidelines and company standards. This role also has....


Three Medical Directors needed The Medical Director is a board-certified physician who has a history of clinical practice, and has significant experience in the cardio therapeutic area, Endocrinology or Renal, Nephrology therapeutic areas. The Medical Director is knowledgeable of the actions of regulatory bodies, in particular FDA, and has experience in clinical trials. An ideal candidate should have significant experience in renal cardio disease management and would thrive on proactively....


GLOBAL PHARMACEUTICAL COMPANY IS HIRING A HEAD OF MEDICAL AFFAIRS FOR RENAL Renal Cardio Medical Head (Executive Director) The Renal Cardio Medical Head is a member of the Renal-Cardio Therapeutic Area (RCTA) leadership team and leads the Renal Cardio Core Medical Team. The position can be either a Senior Director or Executive Director based upon the individual's experience. The Medical Lead is knowledgeable of the actions of regulatory bodies, in particular, knowledge of the FDA. He/She has....


Leading Global Pharmaceutical company with office in Waltham Massachusetts Manager, Health Economics & Outcomes Research (HEOR) Position Summary: The Manager for Health Economics & Outcomes Research (HEOR), will be responsible for supporting HEOR activities for company's products. This individual will contribute to evidence generation, development of strategy, data analysis and dissemination and support the HEOR Senior team members (Directors, Senior Directors).....

- Bridgewater, NJ

The CTM will work closely with the Director, Clinical Operations and Clinical Development team on the design, execution and oversight of clinical trials (all clinical phases) related to pharmaceutical product development and registration. The CTM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, IIT studies, compassionate use and registries) including data management activities, ensuring that clinical studies are....


Represents Regulatory Affairs for pharmaceutical development projects and marketed products. Responsible for development and communication of all aspects of global regulatory strategy on R&D project teams. Leads team of regulatory professionals to assure successful planning and completion of regulatory activities on a worldwide basis. Responsible for knowledge of regulatory requirements of major regions (e.g. US, EU JP) with responsibility for working with colleagues on a worldwide basis....


Clinical Research Physician Global Oncology Pharmaceutical company is expanding and looking to add an MD Strong base salary and benefits and long term incentives POSITION OBJECTIVE: The Clinical Research Physician will be dedicated to providing a leadership role on a matrix team dedicated to stage appropriate clinical development of multiple innovative compounds. He or she will lead the development of clinical strategies for compounds and drive their successful implementation. Essential Job....

- Cambridge, MA

Exciting science being performed at this Pharmaceutical company. Looking to hire two Clinical Operations Leaders under the direction of the New Vice President Clinical.he Clinical Operation Lead is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Clinical

- Cranford, NJ

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....


The Global Regulatory Team Lead (GRTL) is a Director-level role which is part of the Global Regulatory Affairs (GRA) team based in the US. This position is in Irvine, CA and is part of the Global Strategy team. He/she is responsible for developing long- and short-term regulatory strategies that impact company’s business objectives. Specific responsibilities include: Global Regulatory Team Lead (GRTL) is responsible for developing global regulatory strategy for projects in his/her remit, which....


JAVA SOFTWARE DEVELOPER / SOFTWARE ENGINEER / DEVELOPER Columbia, MD REQUIREMENTS:3+ years of current software development experience with the following technologiesJava and/or JavascriptOracle and/or SQL ServerSQLExperience working for a software development product companyStrong Problem solving skillsAbility to understand and translate business requirementsTeam Based AND individual contributor personality ADDITIONAL SKILLS THAT WILL BE USED IN THIS ROLE - IF YOU KNOW THEM ALREADY THIS IS


Job Description: Our client is in the process of opening a new Pediatric Emergency Department and are looking for several RN's and RN Managers who will care for children with all levels of illness and traumatic injuries. Their new facility will have a great support services including Radiology, a Lab, Pharmacy and NICU Qualifications:At least one year of experience of Pediatric Emergency Department experienceCurrent RN license

101-120 of 189 results