Yale University: School of Medicine: Internal Medicine: Geriatrics Location Open Date Oct 11, 2023 Deadline Oct 10, 2024 at 11:59 PM Eastern Time Description To provide expertise in the design, analysis, and interpretation of ongoing and planned observational studies, clinical trials, and basic research in human aging in a highly productive geriatrics research center. Research Track Expectations: This is a collaborative position, which implies that within 3 years all salary support will come from supporting grants and projects from other individuals and projects from within the Department of Internal Medicine, other Yale departments, YCAS, or external contracts and sub-awards. Promotion will be contingent upon excellent performance of all stated duties as stipulated in the Research Track. To independently propose biostatistical designs and analytical strategies for observational and interventional research at the Program on Aging. To carry out comprehensive statistical analyses for longitudinal observational studies, clinical trials, and basic research experiments, most often working on several studies simultaneously. To assist faculty and others with the formulation and description of appropriate statistical methods, sample size requirements, and best research methods as part of the grant preparation process. To assist investigators in the preparation of research grant applications by writing research methods sections pertaining to data collection, data verification, analysis, and interpretation. To articulate findings orally and in written reports to a diverse group of investigators from a variety of research backgrounds. To collaborate in writing manuscripts for peer-reviewed journals and in preparing reports that summarize the analysis of research data, interpret findings, draw conclusions, and make recommendations for future research. To present talks, lead seminar discussions, and make other presentations of the methodologies and analyses used at the Program on Aging at both local (Yale and surrounding region) as well as at national meetings such as the American Geriatric Society (national meeting in May) or the Gerontological Society of America (national meeting in November). To interact with internal contacts such as principal investigators, research project teams, clinicians, and data management staff to provide statistical input required in the design, conduct, and analysis of scientific research studies. To interact with external contacts such as subcontractors and research staff at other institutions to prepare grants, analyze data, interpret findings, and write and edit material for publication. Qualifications Required Education and Experience: A Ph.D. in Biostatistics, Epidemiology, or relevant field. It is strongly preferred that the candidate has at least three years of experience in the medical or biological sciences. Experience with epidemiologic studies or clinical trials, involving both categorical, count, and continuous outcomes, and experience in longitudinal modeling and methods for missing data. Abilities and Skills: Candidates must be able to communicate well, both orally and in writing, and to work well with investigators having different clinical and epidemiologic backgrounds. Candidates must be able to work independently and creatively in developing testable hypotheses. Candidates must be able to set working priorities among various conflicting demands and work concurrently on several projects. Proficiency in SAS is preferred and the ability to use other statistical software (e.g., R, Stata, M-Plus, MATLAB, OpenBUGS) is highly valued. Competence in applying several methods among the following is expected, e.g., generalized linear models, survival models, mixed effect models, structural equation modelling, and Bayesian statistics. Competence in joint modeling, multistate models, latent class models, dyadic analysis, or growth mixture models, is desirable. Competence in the design of experiments, psychometrics, and instrument development is also desirable. Candidate must be open to learning new analytical approaches, software, and to presenting information to the Yale Program on Aging and to sponsoring investigators. Application Instructions Review of applications will begin immediately and continue until the position is filled. All applications, including CV and a letter describing qualifications, should be submitted electronically to:http://apply.interfolio.com/134327 Application Process This institution is using Interfolio's Faculty Search to conductthis search. Applicants to this position receive a free Dossieraccount and can send all application materials, includingconfidential letters of recommendation, free of charge. Yale University is an Affirmative Action/Equal Opportunity employer. Yale values diversity among its students, staff, and faculty and strongly welcomes applications from women, persons with disabilities, protected veterans, and underrepresented minorities. #J-18808-Ljbffr

ONSITE 5 DAYS, NEW HAVEN ONLY, PARKING WILL BE REIMBURSED.This is what you will do:The position is required to join Injectable Drug Product Development group of *** pharmaceuticals' Analytical and Pharmaceutical Development department. This position is required to conduct studies to enable Drug Product characterization activities, including combination products at high protein concentration, as well as commercial products. The job entails experimental work on various aspects of Drug Product characterization, including formulation development, safety risk assessment of excipients as well as process reagents, extractables and leachables, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, particulates testing. The ability to work with minimal supervision as well as part of the team is essential. The position entails execution of the studies and data processing and compiling to generate and support development reports as well as other required documentation. Understanding of assay development, biotherapeutics development is a plus. Understanding of the basic principles of protein chemistry and/or drug product process is required. Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) and familiarity with design and maintenance of databases will be a plus.You will be responsible for: Execute development studies for Alexion pharmaceuticals' drug candidates and commercial products, support tech transfer activities for internal manufacturing and contract manufacturing sitesssist in preparation of internal technical reports on the executed studies with minimal supervision for the Alexion product candidatesParticipate in Department meetings and other technical and team building activitiesYou will need to have: BS in Chemistry, Biochemistry, Biophysics, Chemical engineering, or relevant field with 2+ years of experience or MS degree with 1+ years of relevant experience is required. Solid background in protein chemistry, chemistry, biochemistry, or equivalent is highly preferred.Position requires scientific and practical knowledge of protein chemistry or drug product processPrevious experience in biotherapeutics development as well as understanding of the biotechnology products life cycle and factors impacting protein molecule stability is a plusHands-on experience with instrumentation, used in protein pharmaceutical and analytical development as well as characterization and knowledge of cGMP and quality guidelines is a plusbility to take initiative in problem solving and finding solutions to scientific challenges with minimal supervision is preferredShows ability to take instructions and execute experiments and other activities with minimal supervision is requiredThe individual must be able to work in a collaborative setting and has ability to adhere to timelines with minimal supervision is essentialExcellent interpersonal skills are required, as is the strong ability to communicate effectivelyNesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.#J-18808-Ljbffrby Jobble

The Sadeghi lab at Yale Cardiovascular Research Center (New Haven, Connecticut) is recruiting new members to investigate the molecular mechanisms of aortic aneurysms, angiogenesis, and fibrocalcific aortic valve disease, and to develop related therapies and molecular imaging techniques.We work in a collaborative, interdisciplinary, translational research environment that provides a unique opportunity for professional development. This is achieved through independent research as part of a multidisciplinary team of investigators with many opportunities to advance technical and communication skills, expand discipline-specific knowledge, and gain broad familiarity and expertise in complementary fields of science.The qualified candidates have a MD and/or PhD degree in vascular biology, molecular biology, biochemistry, imaging sciences, bioengineering, or related fields and a track record of high quality publications. Ability to work in a team environment and strong communication and interpersonal skills are essential. Experience in animal work is preferred.Please send CV and a description of career goals and achievements by e-mail to:Mehran M. Sadeghi, MDmehran.sadeghi@yale.eduhttps://medicine.yale.edu/lab/sadeghi/research/

ONSITE 5 DAYS, NEW HAVEN ONLY, PARKING WILL BE REIMBURSED. The position is required to join Injectable Drug Product Development group of Client pharmaceuticals' Analytical and Pharmaceutical Development department. This position is required to conduct studies to enable Drug Product characterization activities, including combination products at high protein concentration, as well as commercial products. The job entails experimental work on various aspects of Drug Product characterization, including formulation development, safety risk assessment of excipients as well as process reagents, extractables and leachables, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, particulates testing. The ability to work with minimal supervision as well as part of the team is essential. The position entails execution of the studies and data processing and compiling to generate and support development reports as well as other required documentation. Understanding of assay development, biotherapeutics development is a plus. Understanding of the basic principles of protein chemistry and/or drug product process is required. Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) and familiarity with design and maintenance of databases will be a plus. Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Research Scientist Jobs in NEW HAVEN, CT

Associate Research Scientist Yale Program On Aging
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Research Scientist Jobs in NEW HAVEN, CT

Associate Research Scientist Yale Program On AgingMay 2, 2024

Research ScientistApril 22, 2024

Research ScientistApril 19, 2024

Research ScientistApril 17, 2024

Yale University Postdoctoral Fellow Or Associate Research Scientist In Valvular And Vascular Biology And ImagingApril 15, 2024

Research ScientistApril 13, 2024

Research ScientistApril 12, 2024