• Merck & Co. (North Wales, PA)
    …ongoing support to job owners and agency partners on promotional review processes and systems, help job owners navigate complex situations, conduct ... operations-based meetingsActively identify areas for opportunity in the promotional review and label update processes and collaborate with the Medical… more
    HireLifeScience (07/12/25)
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  • UnitedHealthcare (Wichita, KS)
    …Complex cases will have additional oversight by masters level case manager, including review of assessments and care plans What are the reasons to consider working ... Health Saving account Dental, Vision, Life& AD&D Insurance along with Short-term disability and Long-Term Disability coverage 401(k) Savings Plan, Employee Stock… more
    Upward (07/25/25)
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  • UnitedHealthcare (Wichita, KS)
    …Complex cases will have additional oversight by masters level case manager, including review of assessments and care plans Youll be rewarded and recognized for your ... national origin, religion, age, color, sex, sexual orientation, gender identity, disability , or protected veteran status, or any other characteristic protected by… more
    Upward (07/25/25)
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  • Eisai, Inc (Nutley, NJ)
    …and oversees JReview and SAS program development for clinical data processing, data review reports and listings. This includes but is not limited to: Program design ... support to other areas of Data Operations, Data Management, Clinical Safety Data Review and Clinical team. The Assoc. Director of Clinical Programming will oversee… more
    HireLifeScience (06/06/25)
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  • AUROBINDO (Dayton, OH)
    …procedures. Document work clearly and perform tests accurately.5. Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.6. Perform maintenance and ... chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.9. Review of Analytical documents as requiredQualifications - Skills & Requirements… more
    HireLifeScience (07/23/25)
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  • Eisai, Inc (Nutley, NJ)
    …strategic plan for assigned therapeutic area(s). These deliverables include development and review of compliant scientific exchange materials to be used in external ... and other senior-level medical communication initiatives as needed.Manage and support the review of SEM and internal medical documents through Medical Review more
    HireLifeScience (06/28/25)
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  • Eisai, Inc (Raleigh, NC)
    …collaboration across teams.ResponsibilitiesExecute core processes within Quality area: Review manufacturing batch records for completeness, accuracy, and compliance ... quality assurance functions in a GMP setting (eg, batch record review , SOP writing, auditing, batch release functions, deviation investigation and resolution,… more
    HireLifeScience (07/24/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and dissemination across CSPV stakeholders for impact assessment. Participates in the review and management of monthly, quarterly, and ad hoc PVRI reports received ... Contribute to overseeing and setting standards for PV contract management. Review contributes to revision of DSI contracts under negotiation (eg development,… more
    HireLifeScience (07/04/25)
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  • Merck & Co. (Durham, NC)
    …GMP, and calibration/maintenance procedures.Uses the SAP work order system to review work requests, identify required stock and non-stock materials, ensure ... to be in compliance and up to date with calibration orders. Review 's vendor calibration certificates.Maintain secondary and or working calibration standardsEducation… more
    HireLifeScience (07/25/25)
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  • Merck & Co. (Rahway, NJ)
    …scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with ... in rheumatologic disorders, preferably autoimmune/immune mediated disease trials.Experience with review of participant eligibility for trials (eg, inclusion and… more
    HireLifeScience (07/25/25)
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  • Merck & Co. (Rahway, NJ)
    …tools, and requirements for all dosage forms (liquid, lyo, drug-device combinations) Review and approval of data and technical documentsAbility to recruit, select, ... and other functional areasExperience with regulatory submissions including writing / review of regulatory filings including INDs and NDAs.Exposure to project /… more
    HireLifeScience (07/24/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …oversight of technical, qualification, and validation activities including data or document review and approval as needed. This role will be responsible for ... within the siteReview and approve qualification/validation documentation (specifications, protocols, reports). Review and approve periodic review documentation for… more
    HireLifeScience (07/02/25)
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  • Merck & Co. (Durham, NC)
    …to support investigations and develop appropriate CAPAs which lead to program improvements. Review and approve out of tolerance (OOT) records and ensure quality ... Maintenance, Deviation Management, Quality and other Site Business Partners.Initiate, Review or Approve changes in the Calibration system (ProCal).Manage approved… more
    HireLifeScience (07/23/25)
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  • Merck & Co. (Durham, NC)
    …to support investigations and develop appropriate CAPAs which lead to program improvements. Review and approve out of tolerance (OOT) records and ensure quality ... Maintenance, Deviation Management, Quality and other Site Business Partners.Initiate, Review or Approve changes in the Calibration system (ProCal).Manage approved… more
    HireLifeScience (07/23/25)
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  • Eisai, Inc (Nutley, NJ)
    …IV clinical development programs for assigned products. Create IIS strategies and review proposals in conjunction with company policies. Participate in review ... key internal business processes including active participation in relevant medical review committees.Work with key internal stakeholders to support development and… more
    HireLifeScience (06/27/25)
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  • Merck & Co. (South San Francisco, CA)
    …clarity, accuracy, and conciseness of regulatory documents to facilitate the review process. -Implement strategies to leverage GenAI for improving document quality ... positive change. -Experience with regulatory submissions and understanding of the review process. -Familiarity with cloud-based data platforms and technologies (eg,… more
    HireLifeScience (07/22/25)
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  • Eisai, Inc (Nutley, NJ)
    …medical accuracy of Eisai's materials; this may include assisting with review of Eisai's advertising and promotional and/or medical/scientific materials. May partner ... Inquiry Resolution, Literature Evaluation, Medical Information Writing Skills, Medical Review , Mentoring/ People Development, Resource Planning & ManagementEisai Salary… more
    HireLifeScience (07/17/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …processes globally. This role will be responsible for coordinating the authoring, review and approval of new or updated procedural documentation. In addition, this ... completing requests/initiatives from the GSOP Committee)Proactively manage required periodic review for controlled proceduresEnsure global and cross-functional consistency of… more
    HireLifeScience (05/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as needed.ResponsibilitiesContract Coordination: Collate exhibits to create contract draft, review contract documents for completeness and accuracy; ensure compliant ... and update CLM system/trackers throughout the process.Conduct Simple Negotiations: Review contractual amendment details against original contract. Ensure internal… more
    HireLifeScience (05/02/25)
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  • BioAgilytix (San Diego, CA)
    …new analytical techniques and technologies and lead their implementation. Review analytical instrument and equipment calibration, qualification and maintenance ... records.Perform statistical analysis.Write and review reports and prepare SOPs.Fulfill the role of Bioanalytical...Insurance, Flexible Spending Account (medical; dependent care), Short Term Disability | Long Term Disability Life Insurance,… more
    HireLifeScience (07/07/25)
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