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Working in collaboration with the federal Office of Refugee Resettlement, our HS/PRS program provides support and assistance to families in need of Home Study Services, and families in need of Post Release Services (PRS.
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The Alaka`ina Foundation Family of Companies (FOCs) is looking for a Molecular Virology Associate Study Director to support our government customer located in Ft Detrick, Maryland. Molecular Virology Associate Study Director.
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Following annual calendar, plan special services (several week Bible study in fall and spring, pro-life event at Queen of Martyrs, RCIA sacramental preparation for Easter Vigil reception of sacraments.
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Education QualificationsAssociate's Degree Nutrition or similar field of study RequiredBachelor's Degree Nutrition or similar field of study PreferredExperience QualificationsPrior work experience in a hospital setting or WIC program PreferredSkills and AbilitiesAbility to communicate effectively verbally and in writing to patients and families, public, medical staff and physicians.
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Develop/facilitate additional training activities including training on amendments to core study documents Perform ongoing data management review; Ensure site adherence with data entry timelines/expectations and overall data quality/completeness Work collaboratively with the Data Management team to plan/execute database amendments Support data review/reporting for analysis, presentation, publications, etc.
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Bachelor's degree and 1-3 years of relevant experience in fast-paced fundraising environment or equivalent combination of education and experience required, preferably in institutional development or a related field, with exposure to development communications, prospect management, annual giving, major gifts, volunteer engagement, and stewardship.
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As a Senior Statistical Programmer, you’ll have the opportunity to design and write program specifications for CDISC conversions, revise programs for corrections, independently create agency-accepted eSubmission deliverables, review statistical analysis plans and study documents and provide feedback to Biostatistics.
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The Study Director, Research Scientist will have a passion for preclinical research. Three years experience as a Study Director for in vivo studies (including GLP) in a biopharmaceutical company or Contract Research Organization (CRO) One to two years experience in Toxicology a plus.
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Work/Life Balance Programs including Adoption/Surrogacy/Infertility Assistance, Backup Care through Bright Horizons, Phase Back to Work and Support for New Mothers. The opportunity to support wide-ranging volunteer programs, + 1 day volunteering leave per year, matched personal donations to non-profit organizations dollar-for-dollar, up to $5,000.
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K nowledge or experience in health, HIV /AIDS , reproductive justice and women’s rights, racial justice, mental health, or substance use disorders demonstrated through prior work experience and/or volunteer work.
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The Director will lead a team of full- and part-time employees including head and assistant equestrian coaches/instructors/trainers, office staff, barn maintenance staff and work-study students.
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Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout. Working knowledge of all functional areas of exploratory development, including chemistry/biochemistry, biology, toxicology, CMC, translational medicine, early clinical development, regulatory, etc., and demonstrated ability to successfully and effectively cooperate, collaborate and work across functions.
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A minimum of 3 years of work experience, ideally to include an Endowment or Foundation investment management organization; alternatively, work experience at a public auditing firm, hedge fund or private equity firm, with a strong interest in pivoting careers to an Endowment or Foundation.
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Awesome opportunities to volunteer through Mars Volunteer Program, like volunteering at coral reef cleanups or on research vessels! A supportive work environment is important at Banfield, and we cultivate a culture and team based on collaboration, networking, and lifting one another up.
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Supports clinical trial readiness by working with clinical operations and CROs as needed for generation/review/editing of clinical study documentation including IRB/IBC communications/responses, study manuals, etc.
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study volunteer work jobs Company: National Gallery Of Art
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