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The position is responsible for planning and preparing complex medical device regulatory submission documents for US, Canada, and EU regulatory filings. Provides support for other global regulatory filings. Utilizing detailed, in-depth understanding of medical device regulation leads anticipates in goal regulatory teams, interprets regulations, and provides regulatory guidance. Support management with regulatory programs planning and implementations of departmental strategies and policies.


The Systems, Analytics and Reporting Associate oversees and ensures the successful execution of tasks related to the reporting and visualization of metrics and analytics for clinical, functional, and business operations areas. The Associate is also responsible for metrics, reporting, collection of requirements, leading of meetings, and generation of dashboards or reports. Requirements BS/BA degree in Computer Science, Life Science or Engineering (2-3 years experience) Spotfire experience....

- Farmington Hills, MI

Software Project Leader Farmington Hills, MI Summary of the Software Project Leader: A Software Project Leader is needed to play a vital role in the management and coordination of the multiple phases of ECU software development for automotive transmission and engine embedded controls and applications for one of our clients in Michigan. This client is a market leader in developing next generation vehicle technologies for powertrain, hybrid, stability controls, and other related systems. In this

- Farmington Hills, MI

Lead Software Engineer Farmington Hills, MI Summary of the Lead Software Engineer: A Lead-level Software Engineer is required to play a key role in the development of the software component designs for automotive ECUS and map software functionality onto hardware resources for one of our clients in Michigan. This client is a market leader in developing next generation vehicle technologies for powertrain, hybrid, stability controls, and other related systems. In this position, you will be....

- Syracuse, NY

Part Time MRI Technologist needed for private practice.Perform a variety of MRI procedures to produce quality images for diagnostic purposesProvide a safe environment for all personnel and patients in relationship to the MRI unitProvide complete and accurate documentation of patient and scan information to the facilityMeet the standards set forth by the facility and follow all policies and procedures set forth by suchDemonstrate the ability to build collaborative relationships with peers,....


IMAGING CENTER (ACR Accredited) in Syracuse, NY. This Private Practice is seeking a Temporary Diagnostic Radiologic Technologist / DRT with ARRT certification. Minimum work experience of two (2) years is required. * COMPENSATION is $25.00 per hour. * EQUIPMENT is a GE DR * Diagnostic Radiologic Technologist / DRT WORK SCHEDULE (approximate) is forty hours per week beginning immediately. Monday through Friday DAYS, may include all of the following shifts: 7:30 am to 4:00 pm, 8:00 am to 4:30 pm....


A Private Imaging Practice (ACR Accredited) is seeking a PRN, part-time Magnetic Resonance Imaging Technologist / MRI (ARRT Certified Tech). * COMPENSATION is $38.00 per hour * MRI - Magnetic Resonance Imaging Technologist JOB TYPE is indefinite/PRN, Part-time. * WORK SCHEDULE for the MRI - Magnetic Resonance Imaging Technologist (approximate): Hours are approximately 11 hours per weekend. Saturday evenings and Sunday evenings, 3:00 pm to 8:30 pm evenings. * LICENSE, EDUCATION & EXPERIENCE


Overview Our client is seeking an External Innovation Expert (Scientific R&D) who will work with the company’s R&D to manage complex, cross-functional initiative efforts that require integration and distillation of inputs into a singular, cohesive view. The company may acquire, co-develop and/or invest in new clinical stage assets that enhance their portfolio and exposure to new innovation, resulting in tighter integration of internal R&D efforts with BD. Job type: W-2 contract....

- Waupin, WI

Provision of pharmaceutical services for offenders in Wisconsin's correctional system through the Bureau of Health Services Central Pharmacy Service in a manner consistent with professional standards and comparable to services delivered in non-correctional settings. Prepares, fills and dispenses prescriptions for drugs, chemicals and supplies on receipt of a proper order from a prescribing practitioner for an inmate/student. Prepares and fills extemporaneous prescriptions and orders....


Software Engineer - Passive Safety Southeast MI Job Summary of the Software Engineer - Passive Safety: An Embedded Software Engineer is required to play a vital role for the design and development of the real-time, embedded electronic controls software systems for automotive and safety critical applications. This is a stable, growing company offering significant future opportunities to break into new technologies. If you have a good experience with C/C++ Programming, CAN and....


PHARMACEUTICAL COMPANY: focused on cns and GI and anti-infective The growth of this Corporation has created a unique opportunity for a variety of positions in Northern New Jersey, accommodating staff in Clinical Operations, Data Management, Biostatistics, Clinical SAS Programming and Regulatory. The Clinical Trials Manager will be able to organize and facilitate the overall planning, coordination and general performance of clinical trials that support the Clinical Development Plan for Clinical


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....


Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....

- Cambridge, MA

Global Company is hiring a Senior Leader Clinical Operations Biotechnology company specializing in the detailed structural analysis of complex drugs and is headquartered in Cambridge, MA. Company is applying its technology to the development of generic versions of complex drugs, biosimilar and potentially interchangeable biologics, and to the discovery and development of novel therapeutics for oncology and autoimmune indications This position will be responsible for initiating and leading....


Plan and prepare complex medical device regulatory submission documents for US, Canada, and EU regulatory filings. Provide support for other global regulatory filings. Utilizing detailed, in-depth understanding of medical device regulations, leads and participates in global regulatory teams, interprets regulations, and provides regulatory guidance. Supports management with regulatory programs planning and implementation of departmental strategies and policies.

- Woodlawn, MD

Technical Trainer Employment Type: Contract - Long-term Location: Woodlawn, MD Responsibilities for this position will include: - Identify training needs and assess strengths and weaknesses of existing training programs - Deliver technical training material effectively to different audiences - Propose and develop additional technical training material - Interface with senior leadership to communicate technical material and training objectives Minimum knowledge, skills, abilities. - Bachelor’s....

- Kansas City, MO

The Staff Accountant/Analyst in our Pharmacy group will perform reviews of Medicaid pharmacy cost of dispensing surveys, communicate with providers via phone and email; and prepare written documents supporting professional decisions.Essential Functions:Perform review of pharmacy financial information and assist in help desk operations for pharmacy service projects.Prepare working papers to document scope and findings of work in accordance with Medicaid or other government program regulations....


JOB DUTIES IN ORDER OF IMPORTANCE:(These duties are illustrative only. Incumbents may perform some or all of these duties or other job-related duties as assigned.)May be required to work at more than one institution. Provides program direction by acting for superior & by relieving superior of most difficult administrative duties; organizes, plans, develops & implements a comprehensive medical, mental health & recovery services quality assurance evaluation & monitoring program....

- Springfield, VA

Minimum Qualifications:Paralegal CertifiedAssociate’s degree or higher4 to 6 years of experience in the legal environment Requirements: At this level, the contractor assists in the development of cases by performing the following duties:Analyzes and evaluates case files against litigation worthiness standards.Notes and corrects case file deficiencies (e.g. missing documents, inconsistent material, leads not investigated) before sending the case on to the concerned trial attorney.Reviews and....

- San Francisco, CA

Scope of Work:The Contractor will independently provide services to satisfy the overall operational objectives of the United States Attorney’s Office, Northern District of California. Contractor services are required to support the administrative needs of everyday technical tasks by supporting the Information Technology (IT) staff and assisting to solve minor computer-related problems. Support is required largely in the Administrative Division’s Information Technology (IT) Section to provide....

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