- Merck & Co. (Rahway, NJ)
- …Upstream and Downstream Process Development & Engineering. The latter two together form our Biologics' Process Development (BPD) group. This job posting covers ... opportunities for the BPD group. -We are actively looking for highly motivated people with a passion for innovation and interest in contributing to upstream and/or downstream bioprocessing.Responsibilities include but are not limited to: Innovation Develop… more
- Merck & Co. (North Wales, PA)
- …domestic and internationalWrite or answer routine correspondence as directed, ie, form letters with mail mergeMaintain daily calendars, ie, meeting scheduling ... (internal and external meetings), teleconferencing, video conferencing, accepting on behalf of managementEnsure accuracy (ie, proofreading, grammar)Maintain databases, general and department or Division specific applicationsRegularly perform independent basic… more
- Merck & Co. (Rahway, NJ)
- …setting, or other setting Broad experience in global benefits area Ability to form effective working relationships at all levels of an organization Ability to ... exercise judgment to drive decisions on routine and non-routine matters within area of practice Ability to further business objectives and appropriately balance divisional/function/corporate business objectives and legal risks on global benefits issues… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …statusDeliver transparent, timely and effective communication to teams in the form of data/metrics reporting and trend analysesFoster a collaborative and productive ... work environment, promoting teamwork and continuous improvement.Influence others beyond own scope and level; lead communications with all levels of stakeholders to enable informed decision makingRequirementsMinimum: Bachelor's degree in Supply Chain, Logistics… more
- Merck & Co. (Rahway, NJ)
- …Upstream and Downstream Process Development & Engineering. The latter two together form our Biologics' Process Development (BPD) group. This job posting covers ... opportunities for the BPD group.- We are actively looking for highly motivated people with a passion for innovation and interest in contributing to upstream and/or downstream bioprocessing.As a Scientist in BPR&D, you will work with immensely creative and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the preparation of regulatory submissions. Responsibilities include: review Case Report Form (CRF) annotation and Study Date Tabulation Model (SDTM) dataset, ... identify data inconsistencies and support data review, review analysis dataset specifications and ensure correct interpretation of SAP, develop independent programs to validate analysis dataset and TLFs generated by vendor, ensure analysis dataset in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to solve complex study problems.Responsibilities:Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, ... Results Interpretation, and clinical study report (CSR): Executes statistical activities for low to medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, data surveillance review,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …copy coordination with broader DSI Corporate Communications team).Oversee website intake form to manage all copy updates and page compliance requirements.Develop ... strategy in partnership with IT for "future build" of holistic company newsroom including automating of press release publishing.Develop overarching website optimization strategy including SEO, SEM, search term and key word purchasing (DS.US homepage, newsroom… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …from a physician's perspectiveMay provide clinical input into the eCRF (Case Report Form ) design, participate in the UAT (User Acceptance Testing) and CCG (CRF ... Completion Guidelines) reviewConducts clinical data review per Integrated Data Review Plan (IDRP)Accountable for the assessment of protocol deviationsDiscusses medical eligibility questions and answers safety questions (dose modifications, discontinuations,… more
- Merck & Co. (Rahway, NJ)
- …of drug substance, intermediates and drug product, crystallization, form selection and/or solid-state characterization of organic small molecules,Preferred ... Experience and Skills:- Encourages innovative thinking/risk taking and eliminates obstacles to implement change.-Experience in late-stage development, including API attributes definition, solid-state methods development, validation and/or transfer in support… more
- Eisai, Inc (Nutley, NJ)
- …Provides support for document preparation and follow-up ( eg Informed Consent Form , eTMF fling plan, Co-Monitoring Plan) Creates Clinical Trial Agreement requests ... using the legal tracker and follows-up on original agreements and amendments. Upload to Epic site Coordinates reviews for essential materials such as ICFs and Co-monitoring plans CRO and Vendor Contributions: Assist in managing ancillary supplies with vendor/… more
- Shimadzu Scientific Instruments (Durham, NC)
- …search firms to any employee at Shimadzu via email, the Internet or in any form and/or method without a valid written search agreement in place for this position ... (and agency was requested to work the requisition) will be deemed the sole property of Shimadzu. No fee will be paid in the event the candidate is hired by Shimadzu as a result of the referral or through other means. EEO Statement: Shimadzu Scientific… more
- Aequor (Seattle, WA)
- …laboratory notebook documentation Summarize and present data in group meetings and in written form Ability to work independently as well as with other members of the ... team or across teams to perform and troubleshoot experiments or assay performance Be motivated and show initiative to learn and willingness to work with new technologies Promote inclusive communication and continuous improvement. Perform required trainings on… more
- Shimadzu Scientific Instruments (Atlanta, GA)
- …search firms to any employee at Shimadzu via email, the Internet or in any form and/or method without a valid written search agreement in place for this position ... (and agency was requested to work the requisition) will be deemed the sole property of Shimadzu. No fee will be paid in the event the candidate is hired by Shimadzu as a result of the referral or through other means. EEO Statement: Shimadzu Scientific… more
- Merck & Co. (Rahway, NJ)
- …plans and strategies to various audiences in both verbal and written form , steer and influence interpretations (including impact) and conclusions for reports and ... regulatory documents that are clear and conciseDemonstrated external visibility in the field of pharmacometrics, through publications, presentations, and involvement in professional organizationsExperience in developing quantitative strategies impacting… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …science discipline or a related field.Expertise in scientific protocol and consent form writing/editing, as well as working with IRBs for protocol management across ... the study lifecycle. Demonstrated expertise in technical and scientific writing.CCRP, CIP or related clinical research/IRB certification.Experience in personnel management for maximal productivity, team work, team communication and supervisory skills.Physical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to solve complex study problems. ResponsibilitiesProtocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results ... Interpretation, and clinical study report (CSR): Leads statistical activities for medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Operations (RO), and other key stakeholders (eg Protocol Amendments, Form 1572s, Information Amendments, Meeting Requests/Background Materials, DSUR, IND/NDA/BLA ... annual reports, BTD request etc.).Develop less complex Module 1 regulatory documents (eg cover letter, FDA forms, administrative information, letter of authorization, etc.) for US regulatory submissions.Support FDA meeting preparation including preparation of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …a variety of instructions furnished in written, oral, diagram or schedule form .Follow instructionsSolve practical problems and deal with a variety of concrete ... variables in situations where only limited standardization exists.Add, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.Knowledge and ability to operate manufacturing, manufacturing-support and lab… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …solve complex study problems. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results ... Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results… more
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