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Applicants must possess a Master of Divinity degree or equivalent educational qualifications as evidenced by a graduate-level theological degree from a college, university or theological school accredited by a member of the Council for Higher Education Accreditation (CHEA) or Association of Theological Schools (ATS) and recognized by the U.S. Department of Education.
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The Court Services and Law Libraries Department is responsible for providing key court services to support the administration of justice and advance access to justice in the Trial Court. Maintains the ability to perform Law Library Assistant I duties in at least one other Trial Court Law Library.
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This opportunity is to support the Clinical Trial Division within the Pharma Services Group (PSG) of Thermo Fisher Scientific. Research, identify and qualify Cell & Gene Therapy companies within our given territory for fit with PSG services.
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Serve as the GLP/GCP subject matter expert to cross-functional clinical trial teams to ensure that all quality and regulatory compliance activities were conducted in compliance with GCPs, SOPs, and ICH Guidelines.
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At least two years to four years of experience in a biological research laboratory is required. A successful candidate will be highly enthusiastic about taking a hands-on approach and will be expected to actively participate in many research responsibilities including, but not limited to, verbal and visual communication of scientific data.
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The Research Associate will need to serve as a clinical liaison between Boston College and partnering agencies in Sierra Leone. The Research Associate supervises and trains a team of 5-10 research assistants at partner organization, Caritas Freetown, and 1-2 Boston College interns.
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A Master of Business Administration degree is a plus. Proficient in utilizing Slack, Gusto/Rippling, Google, Microsoft Suite, LinkedIn, and other relevant software, applications, and social media platforms to enhance operational efficiency.
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Experience in working in cross-functional, multicultural and international clinical trial teams. Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Will play a critical role for a large NIH UM1 center aimed at mapping the human and non-human primate brain atlases using a state-of-the-art technology pipeline consisting of tissue processing methods, molecular probe labeling, volumetric optical imaging, and novel computations 3D image data processing and analysis; undertake engineering design, development, and testing of image processing algorithms and quality control in support of new specialized research instruments.
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Ensure study compliance with Delix’s SOPs and regulatory guidelines by performing periodic quality control audits of the electronic trial master file (eTMF) throughout all study phases including study initiation, implementation, and closure.
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Qualifications: Required Master of Social Work degree from an accredited school of social work State of Massachusetts licensure as an LCSW Preferred Two years of healthcare social work/case management experience CCM or ACM (Commission for Case Management or American Case Management Association) NASW membership FLSA Status: Exempt As a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities.
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Affinia Therapeutics is seeking an In Vivo Research Associate to join our Preclinical Research team. You will be part of a team focused on performing preclinical-stage studies that are essential in supporting our next-generation gene therapy research.
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We are seeking a Research Associate or Senior Research Associate Contractor who will be responsible for developing and performing in vitro studies for mechanism of action and efficacy of novel biological and/or small molecule therapeutic agents, including nucleic based approaches to support drug discovery efforts across multiple programs from target validation to human translation.
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Quality Management Maintain project compliance with corporate and public regulationsMaintenance and Support ProcessFollowing customer acceptance of initial project, transition to maintenance mode, confirming support channelsHelpdeskWeekly delivery confirmation emailMonthly/ check-in meetings with colleagues from customer success and salesRequirements Have a University degree preferentially in Biology or in Pharma, Biochemistry (PhD or master) or related Data-Science Fields.
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Our toolkits for addressing our clients’ research questions include survey research, focus groups, in-depth interviewing, ethnography, and analysis of audience metrics as well as custom methodologies built to suit our clients’ needs.
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trial master file jobs Title: clinical research associate Company: Parexel in Lexington, MA
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