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Responsibilities: Manage project plan for assigned product launch which include working with the project team to create the project plan Set timelines, track milestones, and forecast budgetary and resourcing needs until plan completion Facilitate launch planning process for assigned product Build meeting agenda and conduct project meetings Review project plan periodically with the project team Ensure completion of assigned action items and deliverables in a timely manner Qualifications:....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in the Los Angeles, CA area. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Los Angeles, CA area but....

- Norfolk, VA

TECHNICAL SERVICE REP - Southeast Virginia. Norfolk to Suffock area Note: Client will not sponsor candidates We are now looking for an experienced Technical Service Rep for our Pulp & Paper Segment We are looking for someone to be responsible for promoting and selling the organization’s products, applications and services through on-site support of specific customer account(s) in the Coastal District. The main responsibilities & accountabilities of this role are: Manage chemical....


Seeking Engineers, Technical Sales, or Equipment Service professionals with knowledge of or exposure to water treatment, chemical handling, boilers, cooling towers, capital equipment system installations, and/or commercial HVAC systems. As an Applications Engineer you will work closely with customers and Account Managers in a defined territory to complete service support functions that include equipment setup, inventory control, on-site water analyses, specialty chemical product evaluations....

- Any US State

Clinical Project Manager will support management of a Cardiovascular Stem Cell pivotal clinical trial in the US. The suitable candidate will work under minimum supervision and contribute technical and clinical operations expertise (including onsite and remote monitoring of clinical sites and core facilities). In addition, the candidate will assist in the training of perspective investigators in the pivotal clinical trial and support clinical cases. Travel is anticipated to be approximately....


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 OH, MI, KY, TN and IN. Candidates will ideally be located in Cleveland, but other major cities in the territory will be considered. Qualifications:Must have a Bachelor's Degree in....


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


Education/ExperienceBS in life sciences or related field At least 2 years experience in clinical researchKnowledge of FDA regulations Prior Study Start-Up experience preferredAdvanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook Experience with Adobe Acrobat Professional and Microsoft Access a plusPresentation Delivery ResponsibilitiesExecute study start-up for assigned protocols within company timelines by identifying clinical team needs, Oversee Site....

- Irvine, CA

The candidate is responsible for expeditiously developing and processing raw material and product documentation to meet quality requirements within timelines established for product launch and/or timely project completion.The Master Specifications and Documentation department interacts with various Pharmaceutical groups within the organization and departments such as Quality, Global Pharmaceutical Technology, Regulatory Affairs, Operations, Manufacturing (all sites), Procurement (Sourcing),....


The Associate will be responsible for supporting CTM/OSL and ensuring that all assigned clinical study(ies) are running on time and on budget and are completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all policies and procedures. Requirements: Bachelor’s degree or higher (science degree preferably in science or health-related field) Previous experience of working on a clinical study 1-2 year relevant experience in pharmaceutical industry or CRO....


EDUCATION/EXPERIENCE: - 1+ years of relevant experience in pharmaceutical industry - Science degree in medical or health-related field - Clinical Trial Support/Clinical Study experience - Work effectively in a team/matrix environment - Handle conflict management and resolution RESPONSIBILITIES: - Ensuring that clinical studies are run on time and budget - Ensure compliance with regulatory guidelines - Management of clinical trial documentaiton - Tracking of various clinical trail resources

- Lancaster, PA

IT Infrastructure Engineer (location level) – This person works under IT Operations Manager and works with the various labs around the United States. They are the go-to for Field Service Techs next level support and knowledgeable of software, hardware and HIPAA, GXP, GMP and other lab required compliance activities IT Infrastructure Engineer responsibilities include, but are not limited to, the following : · Develops, coordinates and directs the implementation of standardised applications,....

- Philadelphia, PA

Clinical Research Veterinarian position with my world class, stable, northeast based research organization. They require a DVM/VMD degree from an AVMA-accredited veterinary school and a minimum of 1 year of experience in Laboratory Animal Medicine and USDA accreditation within 6 months of employment. In turn they offer the opportunity to be part of a renowned team of researchers and to contribute to the discovery of life improving/saving treatments for a variety of debilitating diseases along....


SENIOR RESEARCH INVESTIGATOR-Liver diseaseRare opportunity to transition from Academia for a specialist in liver disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide cross-organizational support....

- Philadelphia, PA

SENIOR RESEARCH INVESTIGATOR-TRANSLATIONAL RESEARCHRare opportunity to transition from Academia for a specialist in airway/pulmonary disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide....


POSITION SUMMARY: Independently responsible for the efficient and thorough investigation of process deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process. Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of....


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....

61-80 of 82 results