61-70 of 70 results
Sort By


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....

- 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....


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....


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 –....


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....

61-70 of 70 results