• Sterling Life Sciences (Sterling, VA)
    …needed 7) Provide clinical -scientific input into the development of product labels 8) Review data from clinical trials 9) Provide guidance to managers to ... Review non- clinical , post-marketing safety and clinical pharmacology data , as required 11) Participate...Clinical Research Job, Regulatory Affairs Job, R&D / Scientist Job, Product Manager Job, Medical Device Sales Job,… more
    Sterling Life Sciences (09/30/19)
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  • Sterling Life Sciences (Sterling, VA)
    …Biotechnology Career, Clinical Research Job, Regulatory Affairs Job, R&D / Scientist Job, Product Manager Job, Medical Device Sales Job, Biotechnology Sales Job, ... and coordinate activities of individual departments within the Operations Team 3) Review and analyze activities, costs, performance of Operations groups and forecast… more
    Sterling Life Sciences (09/30/19)
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  • Sanaria Inc. (Rockville, MD)
    …MD biotechnology company working on novel malaria vaccines, has an opening for an experienced Clinical Data Scientist and Manager. The Clinical Data ... all data management operations. Contribute to the review and development of clinical protocols, statistical...with salary requirement and resume to careers(at)sanaria.com, subject line " Clinical Data Scientist ." Candidates must… more
    Neuvoo (10/19/19)
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  • IQVIA (Rockville, MD)
    …Drive the delivery of end-to-end study data quality and integrityMay act as a clinical data scientist for performing data analytics by reviewing the ... meet customer needs. RESPONSIBILITIES Serves as a Subject level Data reviewer (SLDR) and Identify any anomalies...data by performing Subject Level Data Review that require further investigation with the clinical more
    PandaLogic (10/16/19)
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  • IQVIA (Rockville, MD)
    …Drive the delivery of end-to-end study data quality and integrity May act as a clinical data scientist for performing data analytics by reviewing the ... meet customer needs. RESPONSIBILITIES Serves as a Subject level Data reviewer (SLDR) and Identify any anomalies...data by performing Subject Level Data Review that require further investigation with the clinical more
    Neuvoo (10/14/19)
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  • Alphident Technologies Inc (Frederick, MD)
    …Deputy Director of Grants Management. 2.Provide scientific writing support and review of program materials, as requested, including highlights, program book content, ... as well as award successes to the IPT; supporting tasker responses and data calls; supporting award outcome and product analyses; and reviewing program announcements… more
    Neuvoo (10/20/19)
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  • LMI (Frederick, MD)
    …mission outcomes we enable our government clients to achieve. LMI is seeking a Scientist to join our JE-OPETS team. This position requires an Active Secret Clearance ... of Taskers, drafting and reviewing documents, summarizing publications and data , and other related technical duties. Support is to...guide the product team in establishing a link between clinical and non- clinical efficacy, developing a robust… more
    Neuvoo (10/14/19)
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  • Integrated Resources, Inc (Westwood, NJ)
    …OF SERVICES REQUIRED: Under the supervision and guidance of a manager, apply clinical /medical background to review medical conditions; assist and perform coding ... using a standard medical dictionary (MedDRA, WHODD); perform reconciliation between clinical database and CIOMS; review patient records to identify… more
    Neuvoo (10/16/19)
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  • Jazz Pharma (Palo Alto, CA)
    …and get to know Jazz Pharmaceuticals. Responsibilities: Jazz Pharmaceuticals is seeking a clinical scientist to join a development team in central nervous system ... management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials Prepare clinical data and clinical more
    ZipRecruiter (08/29/19)
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  • Jazz Pharma (Palo Alto, CA)
    …and get to know Jazz Pharmaceuticals. Responsibilities: Jazz Pharmaceuticals is seeking a clinical scientist to join a development team in central nervous system ... management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials * Prepare clinical data and clinical more
    Neuvoo (10/20/19)
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  • Frederick National Laboratory for Cancer Research (Frederick, MD)
    …characteristics of reagents Providing timely progress reports to Principal Scientist and preparing/performing presentations for management review Writing ... The Clinical PD Biomarkers Program is responsible for identification...the Doctorate degree Proficient in Microsoft office software, electronic data keeping and management, and basic knowledge of statistics… more
    Neuvoo (10/13/19)
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  • George Mason University (Fairfax, VA)
    …within the Volgenau School of Engineering, is seeking a highly motivated research scientist to work in the area of novel sensor and instrumentation design using ... EEG, Transcranial Magnetic Stimulation, transcranial Doppler), as well as clinical research facilities for cardiovascular, neurosurgery and rehabilitation research… more
    George Mason University (10/20/19)
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  • Aetna Inc. (Wellesley, MA)
    …co-workers make the journey to learn and innovate that much more fun. Tanvi K., Data Scientist - Clinical Analytics Job Details Principal Data ... predict member care journeys. The Principal Data Scientist will join the newly formed Clinical ...Benefit eligibility may vary by position. Click here to review the benefits associated with this position. Candidate Privacy… more
    Aetna Inc. (09/30/19)
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  • AbbVie (Mettawa, IL)
    …in cancer treatment. We are growing our clinical development team and are seeking a Clinical Scientist to be based in Lake County, IL or Redwood City, CA. In ... this position you will: Prepare scientific reports/presentations related to clinical trials and review /contribute to clinical protocols, utilizing expertise… more
    Neuvoo (10/19/19)
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  • Synectics Inc. (New Haven, CT)
    Description: Develop, optimize, validate, and perform biomarker assays in support of clinical trials. Support lead Biomarker Assay Scientist in the development, ... absorbance, fluorescence, and/or electrochemiluminescence. Perform flow-cytometry-based assays and acquire data using BD FACSDiva software. Validate analysis templates using… more
    Neuvoo (10/19/19)
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  • GForce Life Sciences (Del Mar, CA)
    Consultant, Research & Development Scientist , Pharmaceuticals Summary Our client, a clinical stage company that has recently secured funding in a Series B ... lab setting to assist in a variety of R&D projects including a retrospective review of the lab notebook to identify additional patent opportunities. This is an… more
    Neuvoo (10/17/19)
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  • GForce Life Sciences (San Diego, CA)
    Consultant, Research & Development Scientist , Pharmaceuticals Summary Our client, a clinical stage company that has recently secured funding in a Series B ... in a variety of R&D projects including a retrospective review of the lab notebook to identify additional patent...options for other project approaches or experiments. . Internal data presentations within R&D organization. . Expertise and Problem… more
    Neuvoo (10/17/19)
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  • Triphase Accelerator Corporation (San Diego, CA)
    …and drug safety manager/physician in the review , querying and reconciliation of clinical data both in real-time and prior to database extraction Contributes ... trial site personnel. Roles & Responsibilities: Analyzes, reviews, reconciles, and presents clinical data for early development studies Represents Clinical more
    Neuvoo (10/17/19)
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  • Green Key Resources (Montvale, NJ)
    …or healthcare field plus 3 years of experience in job offered. Requires 2 years of medical/ clinical data review , use of I/J Review , Inform, and other ... Responsibilities: Perform review of safety data within Clinical database by reconciling safety report with data information in the clinical database.… more
    Green Key Resources (10/20/19)
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  • Celgene (Summit, NJ)
    …Represent the company in discussions with regulatory authorities and alliance partners Review analytical data for completeness and correctness. Complies with ... to the patients we serve. Responsibilities for a Principal Scientist will include, but are not limited to, the...to build CMC dossier for regulatory submissions as an author/ reviewer . Advanced skills in DOE, Lean and/or Six Sigma.… more
    Neuvoo (10/19/19)
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