Urgent requirement for one of our top clients located in “Fremont, CA”. Please contact me at your earliest convenience, along with job No. CPM_62008 to xxxxxx.xxxxxx@xxxxxxxxx.xxx The Clinical Project manager will provide project management and leadership on the planning, preparation and execution of one (or more) high quality clinical project(s). Lead the Neurovascular clinical project team members toward completion of deliverables in a timely fashion within an agreed project timeline. Internally ..... (continued)

The successful candidate will participate in multi-disciplinary efforts aimed at developing new detection instrumentation including IR Spectroscopy. Specific responsibilities include, but are not limited to: • Developing sensors for detection of chemical agents. • Developing innovative approaches for sensing and detection. • Complying with and ensuring department compliance with company health, safety and environmental policies as well as all applicable U.S. export and security regulations. • Provide ..... (continued)

SHORT SCOOP: Degreed or 2+ yrs exp with MRP and/or ERP systems; working knowledge of RPL, Pick/D3, PHP, ASP & VB plus relational DBs (MySQL etc.) SUMMARY: The Programmer writes, codes, tests, and analyzes software programs and applications. He/she also researches, designs, documents, and modifies specifications throughout the production life cycle, corrects errors in a timely and accurate fashion, and provides status reports when required. RESPONSIBILITIES: * Consistently writes, translates, and codes ..... (continued)

This is an excellent opportunity to be a part of a growing team and work in a progressive environment, Please contact me at your earliest convenience. Urgent requirement for one of our top clients located in “NewYork City, NY”. Please contact me at your earliest convenience, along with job No. RCRA_52408 to xxxxx.xxxxx@xxxxxxxxxxxxxxx.xxx Description: Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. Recognize the ..... (continued)

Urgent requirement for one of our top clients located in “Palo Alto, CA”. Please contact me at your earliest convenience, along with job No. SCRA_50808 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: "MUST HAVE IN-HOUSE CRA INDUSTRY EXPERIENCE" Protocol development and writing, planning, study implementation and execution, conduct/oversight, clinical study monitoring and management, study budgets, CRO/vendor management and reporting. The candidate in this position may act as the Lead CRA/Clinical Project ..... (continued)

If you have a moment, I would appreciate your help in our search for uniquely qualified and specialized professionals. Please take a look and forward this open job on to anyone you think would be interested in the position, or anyone else who could help me find a great candidate. If you are applying yourself then please don’t hesitate to forward your updated resume, availability and your hourly/salary expectations to xxxxxx.xxxxxx@xxxxxxxxx.xxx ASAP since we have multiple immediate requirements. Thanks ..... (continued)

Urgent requirement for one of our top clients located in “Mountain View, CA ”. Please contact me at your earliest convenience, along with job No. SCRA_113007 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Monitor clinical trials, study sites, and clinical data. Ensure compliance with protocol and overall clinical objectives and GCP. Provide project support to clinical programs with minimum supervision. Interfaces with all project/clinical groups and off-site personnel as needed in support of project and ..... (continued)

Urgent requirement for one of our top clients located in “Irvine, CA”. Please contact me at your earliest convenience, along with job No. CTM_112307 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Job Description: Responsible for managing the clinical project team for one or more clinical protocols. Functions as an expert resource for clinical trial monitoring activities. Proposes staffing for new and/or existing projects. Responsible for managing clinical studies in accordance with Company’s SOPs, GCPs, FDA and ICH ..... (continued)

Urgent requirement for one of the our top client located in “Cambridge, MA”. Please contact me at your earliest convenience, along with job No. COM_51607 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Responsibilities: Assists in defining protocol(s) and develops informed consent forms, patient instruction guides, and reviews draft case report forms. Serves as a liaison between company and contract research organizations, core laboratories, field sites, investigators, study coordinators, physicians and staff members ..... (continued)

UG - B.A - Any Specialization, Maths, Statistics;B.Sc - Any Specialization, Agriculture, Anthropology, Biology, Botany, Chemistry, Dairy Technology, Electronics, Environmental science, Food Technology, Geology, Home science, Maths, Microbiology, Physics, Statistics, Zoology, General, Other Specialization;B.Tech/B.E. - Any Specialization PG - M.Sc - Any Specialization;M.Tech - Any Specialization

Department: Quality Assurance Reports To: Manager of Quality Assurance/Systems SUMMARY Responsible for supporting product qualification, process validation, quality planning, Nonconformance/Corrective Action assessment and tracking, Complaint Handling, Technical Engineering Support for all Quality Assurance functions associated with the product(s) of this company. Revisions to current and proposed products/systems will be identified and assessed by the incumbent as required to ensure compliance to ..... (continued)

Department: Quality System & Quality Assurance Reports To: Manager, Quality Systems & Quality Assurance SUMMARY Perform internal audits of the company Quality System and processes, perform external supplier audits of their quality systems and processes, follow-up on corrective action progress and/or effectiveness for audit non-conformances, prepare internal and external audit schedules, serve as an internal compliance/regulation expert and communicate applicable regulation changes to the organization. ..... (continued)

Urgent requirement for one of our top clients located in “Rochester, NY”. Please contact me at your earliest convenience, along with job No. CPL_51708 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Job Description: To independently manage and monitor all aspects of implementation of pharmaceutical clinical studies in accordance with FDA regulations, and ICH and GCP guidelines for clinical research studies and SOPs. Job Duties: Assume project management responsibilities for clinical sites as well as field CRAs assigned ..... (continued)

Urgent requirement for one of our top clients located in “Lafayette, IN”. Please contact me at your earliest convenience, along with job No. CTA_032608 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Company is seeking a Clinical Trials Associate I - IV. The qualified candidate will join our rapidly expanding clinical team and will contribute to the successful design and execution of Phase I - III clinical trials. Primary responsibility is the management of one or more clinical investigations or overseeing ..... (continued)

Urgent requirement for one of our top clients located in “Wilmington, DE”. Please contact me at your earliest convenience, along with job No. CS_290108 to xxxxxx.xxxxxx@xxxxxxxxx.xxx Description: Must be computer literate at a high level and willing to learn new systems; prior data analyst/validation required. Must work well with external customers and be willing to learn about clinical research; prior clinical trial management or CRA experience a plus. Must have excellent teaming and communication ..... (continued)

QA Analyst for a producer of therapeutic peptides for pharmaceutical and biotech uses located in Torrance, CA. Primary Job Responsibilities: Accountable for the non-GMP storage and electronic data base for custom peptides; updating customer files. Accountable for weighing and dispensing of GMP and non-GMP key raw materials to production. Responsible for shipping both GMP and non-GMP products to customers. Responsible for distribution of documents. Makes affective new/revised S.O.P.’s, Master Batch ..... (continued)

Senior Manager, CRA IIs - Kansas City, MO and Blue Bell, PA I am recruiting Senior Manager, CRA IIs for a great biosciences company. The positions are located in Kansas City, MO and Blue Bell, PA. Here are more details: Essential Duties & Responsibilities Supervisory Responsibilities: Supervision of CRA II Manager Oversight of CRA II team Specific Job Duties: Work with CRA II Manager and Project Managers to ensure studies are adequately staffed. Work closely with the CRA II Manager, Sr CRA IIs and ..... (continued)

Scientific Writer for company located in Austin, TX. This position is on-site, 'permanent' and full-time. Here are more details: The scientific writer will be expected to generate grant ideas and collaborate with other senior scientists to develop their ideas and research programs into grant applications. The scientific writer will seek out new funding opportunities to support R&D. The scientific writer will also write or edit articles for peer-reviewed journals, trade publications, and ..... (continued)

I am assisting to recruit a Sr Scientist, ADMET for a great company in New York. Would you be interested in an opportunity such as this? If so, the details are below for your review. Either way, thank you for your time and have a great day! A technology leader specializing in software solutions for life science research and development, is seeking an outstanding computational scientist to manage the development of the next generation of computational tools for predicting ADME/Tox properties. The ideal ..... (continued)

A growing biotech company providing advanced products for molecular biology, is seeking a creative marketing professional with at least 5 years experience and demonstrated success in the research reagents market. Requirements: 1. experience with molecular biology reagents 2. prior supervisory/management experience 3. M.S. in a life sciences discipline required; Ph.D. preferred 4. sales experience highly desirable The Director will lead the Marketing & Sales team in strategic and tactical marketing ..... (continued)