At least three years of experience in client management and project management. Provides strategic, technical and scientific leadership for the execution of these assays for assigned program(s), Collaborates with the Discovery units to ensure timely transfer of biomarker assays to the Translational and Biomarker Research assay group for method development purposes, Independently develops biomarker assays and designs assay validation studies using various technology approaches according to the “fit-for-purpose” principle. Developed web-based application using C#, ASP.NET, and SQL Server for intranet peer recognition program. biotinylation, ruthenylation using standard chemistry), assessing their purity and affinity, and generating Certificates of Analysis, Monitors and or trend lot-to-lot variability, and may assist with reagent troubleshooting, Develop new techniques , or bring in new technology from the outside, to enhance the analytical capabilities of the group, Prepare SOPs, reports and documents such as characterization protocols, development reports, and testing data reports, Independently carry out the aforementioned tasks and plan, implement, and complete significant projects with minimal supervision, Share responsibility for lab management duties, Required: At least 5 years of experience in a laboratory, research laboratory, or biotechnology company working with antibody and protein biochemistry, Preferred: Excellent writing and verbal communications skills, Developing and characterizing patient-derived xenograft mouse models of cancer, running in vivo efficacy studies (including tumor measurements and dosing (IV, IP, PO), and support for PD/biomarker analysis efforts, Executes experiments, conducts analysis and reports results, Other tasks and responsibilities, as assigned, Bachelor’s degree in a scientific discipline with at least 4 years work experience or Master’s degree with at least 2 years work experience, In vivo experience in the biotech/pharmaceutical industry is preferred, Solid understanding of murine in vivo cancer models including monitoring animals, tumor measurements, dosing protocols, and study designs and data presentation is required, Ability to solve problems, work in close coordination with other research scientists, and provide clear and concise result summaries to lab head and small groups is essential, Ability to work in role requiring strong attention to detail and organization is critical, Utilize microscopy, flow cytometry, and other research techniques to test BioLegend reagents in cell biology and immunology applications, Be involved in research and development activities pertaining to novel fluorescent probe development, Analyze flow cytometry data using FlowJo and microscopy data using MetaMorph, Setup functional assays involving cell proliferation, health, function and differentiation according to Standard Operating Procedures (SOP’s), Present data and maintain lab notebook and databases in accordance with all ISO requirements, Support the marketing and web presentation of BioLegend products through application development activities, Have the opportunity to become involved with externally facing marketing opportunities (networking, trade shows), Bachelor or Master degree in life science or related discipline, Minimum of four years of hands-on lab work experience, Experience in immunofluorescence and widefield microscopy is required, Immunohistochemistry, confocal microscopy, and live cell imaging is a plus, Experience in animal dissection and tissue sectioning, Working knowledge or experience with non-antibody chemical probes such as proliferation, subceullular localization, ion indication, potential indication probes, Working knowledge of flow cytometry and immunofluorescence, Experience in flow cytometry and/or microscopy instrument maintenance is a plus, Ability to effectively advance multiple projects simultaneously and to work independently in a team environment, Excellent organization, communication and problem solving skills, Strong marketing and business development skills, Strong analytical ability, logical and problem solving approach on complex issues, In depth understanding of competition and competitor strategies, Technical competence in Tax and also the industry / specialized field, CA/CMA Qualified or Finalist with minimum 3 -5 years of experience in Indirect Tax/ VAT/ Excise, Previous experience in Manufacturing or Service industry, Exposure to regulatory/compliance requirements for Tax in MENA region, O Good Communication skills- both written & Oral, Independently design, optimize, execute and interpret qPCR, ELISA and flow cytometry assays in support of antibody programs, contributing to program strategies and success, BS/BA in a biology-related discipline and 8+ years of related laboratory experience or MS/MA with 6+ years of related laboratory research experience; including a strong working experience with therapeutic antibodies, In-depth technical and theoretical knowledge, and practical experience in, principles and practices of cell biology methodologies and cellular immunology, including mammalian cell culture, cell transfection, functional/in-vitro cellular immunology assays and cellular assay development, Extensive experience in primary mouse, cyno, or human lymphocyte and mononuclear cell purification and functional assays, Ability to maintain productivity and quality results for routine, established assays, while working on multiple projects, tasks, Ability to work on complex problems where analysis requires an in-depth evaluation of multiple factors. No need to think about design details. (20%), Conduct experiments using protocols to lead data collection teams comprising of research associates, research assistants and temporary labor. Direct subjects through the course of day-long participation/ complete study assessments in coordination with other staff or independently based on subject load and staff availability. Skin transplantation in mice (immune mismatch). Writing your resume with a target job in mind requires having a clear understanding of the job's skills and proficiencies. Present clinical information to Principal Investigator; participate in case conferences with PI, psychiatrists, and other staff as needed to reach consensus diagnoses. PRA Health Science - Senior Clinical Research Associate Dallas , TX 01/2019 - Current. Increased responsibility for design and planning of experiments, Applies standard methods to conduct full physical and chemical tests. Must be able to demonstrate good decision-making skills, Must have demonstrated problem solving abilities, Strong organizational skills are required, Working knowledge of MS word, Excel, Power point is required, Experience working in a FDA regulated environment is highly desired, Design and conduct surveys, interviews, observations, and assessments, Manage data including quality control/quality assurance, Analyze qualitative and quantitative data, Lead project tasks, including mentoring junior staff as needed, Interact with and understand client needs, Contribute to Continuous Quality Improvement initiatives, Perform background research on specified topics and synthesize material in the form of literature reviews and final technical reports, Plan focus groups, including recruitment, logistics, note-taking, and reporting, Occasional travel to locations nationwide, Master’s degree in social work, psychology, education, early childhood education, social science, political science, sociology, or related subject, 5+ years of experience in supporting or conducting research in the social science field, preferably in child welfare related issues and/or evaluation of technical assistance or capacity building, Experience with data collection, administering surveys, interviews, focus groups, or structured observations, Experience with managing multiple timelines/multiple tasks, Demonstrated experience in producing high quality written products, Experience with Federal or state government programs, specifically in child welfare, early education, or K-12 education fields, Experience with research related to CFSR and IV-E Waivers, Experience working in a consulting environment, Excellent verbal, interpersonal, and written communication skills, including experience with developing and delivering presentations, Solid team builder and team player with proven ability to manage competing priorities, perspectives and stakeholder needs, Ability to work limited overtime as necessary, Ability to work independently and lead tasks, Demonstrated, outstanding level of professionalism, including ability to exercise good judgment, discretion, tack and diplomacy, Design and conduct surveys, interviews, observations, direct assessments, and focus groups, Identify business development opportunities and conduct meetings with clients, Doctoral degree in early childhood education, psychology, education, social work, political science, sociology, or related social science fields, 5+ years of experience in supporting or conducting research in the social science field, preferably in early childhood education issues and/or evaluation of technical assistance or capacity building, Experience with programs, specifically in early education or K-12 education fields, Lead individual research inquiries and assume intellectual ownership of discrete topics; design analytic frameworks for testing new ideas, Lift out and communicate insights to members, formally and informally, in the form of on-sites, webinars, and other content delivery venues, Coordinate and participate in research interviews with executives, academics, and industry experts; build strong research relationships/sources, Provide excellent written and graphical summaries of key findings; perform in-depth data analysis when necessary, Use analytic tools, such as root-cause analysis, to identify the drivers of advocacy challenges, hypothesize solutions, and isolate differences between conventional and advanced practice, Manage/coordinate response to inbound research inquiries by individual member organizations, Undergraduate degree required; graduate degree strongly preferred, Strong project management, people management, and time management skills, Creative thinking and resourcefulness in problem-solving, Extreme talent in distilling large amounts of information into relevant insight, Ability to ply both quantitative and qualitative analysis skills to identify relevant findings, Excellent oral and writing skills; graphical presentation skills a strong plus, Prodigious work ethic and spirit of generosity, Record of exceptional academic achievement, and an aspiration to constantly learn and improve, B.S. A research assistant resume objective or summary is a short and snappy paragraph that explains why you’re an ideal candidate for this job. May contribute to the development of new concepts, techniques and standards. (with 1-5 years of experience) or B.S. June 2005 – October 2009. Find job openings from companies that are hiring now (and see if they fit you). This way, you can position yourself in the best way to get hired. To engross oneself in such an environment that would provide efficient learning and growth in the professional world. ), Ability to effectively utilize scientific information resources within the assigned area of responsibility, Keen observation skills, demonstrated problem solving, and troubleshooting skills (e.g. To get Research Associate Vacancy 2020 Notification, Upload your resume and subscribe to to know immediately about the latest Research Associate Jobs notification from Fresherslive.com. Review entire subject files of clinical assessments completed by research staff for correctness and completeness prior to data entry and analysis; work with staff and the Principal Investigator to address questions or concerns as needed. Managed space, pest control, and nutrients for 200-300 flats of Arabidopsis resulting in tenfold reduction in loss of plants from disease, insects, and poor plant care. Initiates alternative approaches and modifies existing techniques based on evaluation of research data. in Physical or Life Sciences with a minimum of 4 years of experience, Working knowledge of immunology, molecular biology, biochemistry, or related discipline and technical approaches, Expertise in current instrumentation and analysis techniques and maintenance and familiarity with scientific literature within the relevant scientific discipline, Sound understanding of experimental objectives and concepts of experimental design, Possess organizational, prioritization and general project management skills, attention to detail, and the ability to work independently, Ability to function cooperatively and effectively in a team environment, Possess advanced word processing, data entry, data analysis and presentation skills, Comply with safety practices and standard operating procedures, Exhibit the Global Takeda Core Competencies, Formulation, process development and combination products of biopharmaceuticals including physical, biochemical and characterization analysis such as general appearance, MFI (Micro Flow Imaging), injection force testing, silicone distribution, viscosity, UV-Vis spectroscopy, HPLC, DLS (Dynamic Light Scattering) and CD (Circular Dichroism), Support project lead in commercial drug product technology transfer activities such as, process evaluation, validation documentation writing and review, root cause analysis and risk assessments, Maintaining a laboratory notebook including writing up experiments, data analysis and review, Author study protocols, reports and relevant sections of regulatory submissions, Assist in the set-up and maintenance of a new state of the art lab including ownership of instrumentation and writing equipment operating procedures, as required, Assist in the manufacture of drug product non-clinical and clinical batches, Coordinate with external contracting organization necessary to accomplish DPDO activities, BS or Masters in scientific area with 5 years of experience required, Formulation and/or process development experience including the analysis and characterization of proteins required, Excellent planning, verbal and written skills. The mission of the Research Department at the Democratic National Committee is to ensure Americans get the facts about politicians and their policies before heading to the ballot box. (10%), 7+ years of experience with conducting public health research or evaluation, including study design, data collection, analysis, and report writing, Experience in working with CDC global health, Ability to demonstrate subject matter expertise in public health training or translation, clinical quality, chronic diseases, diabetes, opioid abuse, Ebola, and Zika viruses, MA or MS degree in Public Health or Epidemiology, Produce proteins to the needs of both internal and external programs using transient or stable transfection, Purify antibodies and recombinant proteins uisng FPLC system, Maintain cell lines and cell culture equipment for protein production, Maintain an accurate lab notebook and DNA/ protein database, Proactively communicate results to team and take part in troubleshooting, May be required to perform other related duties as needed, BSc in biology or related field of science with greater than 5 years of industry experience OR MSc in biology or related field with greater than 3 years of industry experience and a strong work ethic, Ability to independently design and execute experimental plans, Demonstrated expertise in transient protein expression, cell line maintenance and protein purification, Skilled at organizing and presenting data and strategy in scientific settings and team meetings, Ability to work at multiple levels with other scientific disciplines in a small company environment, Experience with molecular biology, cloning and site-directed mutagenesis, Research, development and implementation of extended characterization assays for biologics, including: payload-linkers, antibodies and antibody-drug conjugates, Work independently to develop new extended characterization assays as needed and on an ongoing basis, Function as a key contributing member of the Bioanalytical Chemistry team and communicate results across in-house teams, Generate data for strategic partner relationships, for platform development, and to support patents and publications, Maintain an accurate lab notebook and databases as required, BS in biology, biotechnology or related field of science with greater than 5 years of industry experience OR MS in biology, biotechnology or related field of science with greater than 3 years of industry experience and a strong work ethic is required, Demonstrated expertise in separation methods for extended characterization of biologics, preferably including capillary electrophoresis and high performance liquid chromatography, Applicants with experience in and a proven track record with multiple separation methods will be favorably considered, Respond to the needs of both internal and external programs using synthetic organic chemistry to troubleshoot and solve problems in the preparation of bioactive molecules, Maintain an accurate lab notebook to support tech transfer and the protection of intellectual property, Communicate results to the broader scientific community through publications and presentations, Publish results in peer reviewed journals, BS in synthetic organic chemistry or related field of science with greater than 5 years of industry experience OR MS in synthetic organic chemistry or related field of science with greater than 3 years of industry experience, Demonstrated expertise in multi-step synthesis, reaction optimization and compound purification, Competency with modern spectroscopic methods applied to small molecule structure determination including 1H NMR and mass spectroscopy is required, Experience with bioconjugation and/or handling high potency bioactive molecules is a plus, Experience with project goal/milestone setting and project management with skill in working across broad functional teams is a plus, Coordinate global health programs and studies, Provide technical assistance to USG, in-country officials, and public and private partners on program implementation and M&E, Develop and deliver capacity building trainings, Master's degree in epidemiology, global health, public health, public policy, behavioral or social sciences, or related field required and a minimum of four years of working in the public health or global health field, Demonstrated research design and analytical skills, Ability to travel internationally for extensive periods of time required, A minimum of 3 years of experience designing and implementing M&E studies for HIV and/or sexual reproductive health projects, Demonstrated knowledge of PEPFAR monitoring, evaluation and reporting, Experience implementing mixed methods research and/or evaluation studies, Experience using statistical software, such as Stata and/or SPSS required, Demonstrated experience managing projects in low and middle-income countries required, CDC, USAID or other international donor experience preferred, Training development and facilitation experience a plus, Experience using qualitative data analysis software, such as ATLAS.ti and/or MAXQDA a plus, Experience working with wide variety of stakeholders (e.g., Ministries of Health, PEPFAR public and private partners), Language fluency in French, Portuguese, or Spanish preferred, Excellent verbal, interpersonal and written communication skills required, Strong analytical, problem-solving and decision making capabilities required, Excellent problem solving skills with ability to analyze situations, identify existing or potential problems and recommend solutions required, Candidates must have well developed writing skills, Safe, efficient execution of experimental program including preparation of raw materials, processing in various equipment and chemical/physical analysis, Accurate documentation of results in laboratory notebooks and databases. These involve soil preparation, planting arrangement, seed preparation, planting, achieving of all agricultural operations, selection, pollination, harvest , recording and loading data, seed inventory, oil analyses, oversee and leading workers, Using unique skills and procedures, ensures that all material necessary for conducting laboratory or field experiments is prepared properly and on time, Assists with miscellaneous tasks such as cleaning, handling, packaging and storing field or laboratory material, Operates and maintains complex equipment in support of experiments conducted within a research project, May write experimental reports, summaries and protocols, Assist for managing the temporary employees and keep them motivated by sharing responsibilities with crew leaders, Implement DuPont-Pioneer safety programs at the station level. Even though the job tasks vary depending on the employer, the common tasks mentioned on the Senior Clinical Research Associate Resume include – planning and directing clinical research trials and projects, supervising employees, providing staff training, recruiting study participants, screening trial participants through interviews and medical records reviews, monitoring ongoing research activities, designing … Maintains robust experimental records and reports data to supervisor in oral and written reports, Will prepare and maintains stocks of necessary reagents, solutions and supplies. If you're looking for research scientist jobs, a well-researched resume is vital to your search, says resume expert Kim Isaacs. (10%), Interact with members of the data sciences group to develop methods of data collection specific to experiments conducted for prediction agriculture. Summary : Senior Research Associate with a comprehensive background in chemistry, material engineering and general management. Build Your Own Now. May be responsible for leading certain aspects and/or developing non-standard procedures and equipment, Responsible for more advanced data generation and analysis, with some ability to propose next steps. 100%. in a related field with a minimum of 5 years of bioanalytical experience in pharmaceutical, biotechnology, and/or CRO industry, Previous experience in Data Review (QC) in support of large molecule assays is required, Proficiency in Microsoft Office, SoftMax and Watson LIMS, and knowledge on data integrity and regulatory requirements are expected, The candidate must be able to work collaboratively in a diverse, fast-paced environment with ability to multi-task, 3 years experience in developing deep learning solutions focused on face recognition or facial analytics, biometric, identity science, computer vision, and machine learning, 10 publications in the computer vision or machine learning space, 5 years experience in developing solutions for sponsored research in computer vision, biometrics, deep learning, and other machine learning techniques, 5 years experience managing research projects and teams, To oversee and conduct initial research into target organizations and industry sectors to assist in identifying the top talent for our clients’ mid-level managerial roles, Identification and approach of suitable candidates and qualify them against agreed competencies and criteria for each project, Maintain clear and consistent communication with candidates during the assignment, Report writing and preparation of presentations, Capturing and maintaining accurate market, client and candidate information on the company’s knowledge systems, Assisting consultants in drafting advertisements, and screening advert responses, Building relationships within the industry to develop our network for gain candidate referrals, Contributing towards process, career development and training initiatives, Demonstrable experience in Executive Research/Resourcing/Headhunting, or a proven Recruitment Consultant who can demonstrate excellent headhunting skills, Fluency in both Dutch and English (written/verbal), A track record of recruitment sourcing, innovation, and creativity, Strong business acumen and people/communication skills, A deep understanding of the financial sector is required. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position, M.Sc/M.Pharm in Organic Chemistry /Medicinal Chemistry or relevant field/, Expertise – we strive for a deeper understanding of our domain, Innovation – we aspire to do things creatively, To safely and effectively carry out routine synthetic organic chemistry techniques (Reactions, recrystallizations, chromatography) with minor supervision, To conduct routine synthetic organic chemistry reactions with procedures supplied and discussed by supervisor, To maintain a laboratory notebook with clear descriptions of the reaction scheme, stoichiometry, results and observations consistent with SOP, To obtain and interpret simple NMR, IR, and mass spectra, To purify compounds to the required level for submission for biological testing, Has basic understanding of the reactivity and functional group compatibility of the chemical target, intermediates, and reagents employed, Should able apply basic literature research skills, Should able Contributes effectively to experimental write-ups for patents and internal reports, To Maintains awareness of, and provides recommendations on, laboratory tools and procedures as appropriate, Consistently demonstrates moderate productivity in the preparation of straightforward analogs, and is able to do more than one reaction and work-up simultaneously, An understanding of energy materials and high temperature processing equipment, Experience in sample preparation techniques, Experience in electron microscopy techniques, Ability to translate, adapt and apply academic and/or practical knowledge to engineering research, Ability to instruct others on instrument use, scientific principles, and safety, Ability to work with a diverse group of people; Knowledge of good safety practices, Experience in safe handling and managing of radioactive materials, Experience in working in a glovebox environment, Experience in advanced characterization/chemical analysis techniques including FIB/SEM, TEM, EBSD and EDS, Proficiency in the maintenance and use of advanced materials processing techniques, Will be a primary member of a team seeking to developing new technologies for understanding the druggable proteome. 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