- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Cycle Management:Responsible for the ownership and maintenance of GCO-owned procedural document packages.Lead authoring, review , and periodic reviews/updates for ... research areas centered around rare diseases and immune disorders.Summary The Associate Director, Global Clinical Operations (GCO) Procedural Ownership and Life… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …objectivity and discretion in the observation and collection of facts. Conducts document collection, document and information review , interviews and/or ... other research areas centered around rare diseases and immune disorders.Summary The Associate Director, Privacy & Compliance Investigations, is a member of the… more
- Merck & Co. (Durham, NC)
- …to the pharmaceutical industryExperienced in the methods and approaches of conducting document review & quality audits PHYSICAL REQUIREMENTS: Ability to sit, ... shift P1 position on the 2/2/3 schedule. The Shop Floor Quality Assurance Associate is responsible for all Quality related functions that directly support Durham… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and review and author safety sections of Common Technical Document (CTD). May oversee multiple simultaneous submissions to ensure harmonized approach of ... and review and author safety sections of Common Technical Document (CTD). May oversee multiple simultaneous submissions to ensure harmonized approach of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …post trial information on required public forums (eg.clinicaltrials.gov).- Under supervision, review and document CRO-generated reports, such as site monitoring ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
- Merck & Co. (Durham, NC)
- …air sampling, surface sampling and non-viable air sampling.Provide data entry, review and approval as required.Provide summaries of test results to appropriate ... LIMS sample rejections. - Equipment Calibration and ManagementFiling data sheets and document control of logbooks - Other duties requested by Management.In addition,… more
- Aequor (Thousand Oaks, CA)
- …will be required to administer the processing of documents via the established Document Processing Review process. May require communication through a variety of ... Office expertise; previous technical writing experience; regulated environment experience; document version control experience; excellent communication/writing skills Responsibilities Own… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …operational input into study protocol profiles, final protocols and amendmentsLead document review and coordination for the protocol and amendments. ... Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution at… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …that fall under the responsibility of the R&D Procurement group. The Associate coordinates with R&D Procurement team members, Purchasing, Legal, Finance, vendors and ... needed.Responsibilities- Contract Coordination: Collate exhibits to create contract draft, Review contract documents for completeness and accuracy; Ensure compliant… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the ... strategic and planning alignment across regions and functions and supports review of Local Country/Regional Medical Affairs activities when applicable. Provide… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational Medicine, will be responsible for leading the Translational ... include the clinical pharmacology support of the Common Technical Document (CTD) and label, including relevant compound/program life-cycle management.The successful… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... include the clinical pharmacology support of the Common Technical Document (CTD) and label, including relevant compound/program life-cycle management.The successful… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and managing a learning program from content to delivery. ** Prior to applying, review the Education & Qualification section - Be sure you possess the Minimum years ... decks, project status updates, executive summaries and case studies, and document client meetings. Qualifications: Successful candidates will be able to meet… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and CRO).Contribute to operational delivery aspects of the protocol and take a document review & coordination role for the protocol and amendments. Additional ... primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy....implemented. Liaise with CRO to support database lock and review of TLG before and after database lock.Ensure DS… more
- Merck & Co. (Rahway, NJ)
- …regulatory advice and approval according to the committee charters. (Therapeutic area document review committees (DRC), Global Regulatory Team (GRT) Product ... and/or subsidiaries for all applications and submissions.Responsible for regulatory review and final approval of all submissions and associated… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …operational input into study protocol profiles, final protocols and amendments.Lead document review & coordination for the protocol and amendments. ... role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This position may… more
- Duke Health (Durham, NC)
- …reimbursed by payor Communicate with care team regarding high risk patients Review Therapy Admission Clinician Medication Lists Assure Follow-up for patients with ... (not all applicable to Telehealth Nurse): - Plan, provide, supervise and document professional nursing care utilizing the nursing process for patients in accordance… more
- Belcan (Stratford, CT)
- Document Review Associate Job Number: 349037 Category: -MFG & Supply Chain SBU Description: Job Title: Document Review Associate Pay Range: ... months Location: Stratford, CT 06615 Area Code: 203, 860 We're seeking a dedicated Document Review Associate to join our team on a contract basis. This role… more
- Insight Global (St. Paul, MN)
- Job Description Day to Day: The Document Review Associate will be joining the Agency team of 12 to perform Document Review according to standard ... roles) -Bachelors or Associates -Finance experience -Data Entry experience -Mortgage Background - Document Review Specialist Analyst or Review experience… more
- Insight Global (Florence, SC)
- Job Description The Document Review Associate will be joining the Agency team to perform Document Review according to standard procedures or ... savvy, used in previous roles) -Bachelors or Associates -Finance experience -Mortgage Background - Document Review Specialist * Analyst or Review experience *… more
