- Hirewell (Riverdale, GA)
- …Continuously improve sales techniques and professional presentation General Expectations Review trial balance with Credit Manager monthly Maintain a clean ... and organized company vehicle Represent the company in a professional manner at all times, ensuring quality customer service Follow all company policies and applicable safety procedures Support overall company programs, goals, and initiatives Work overtime as… more
- Genmab (NJ)
- …Then we would love to have you join us!The Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as compound ... lead, primarily up until proof of concept, and/or as trial responsible statistician.Responsibilities:Compound/Indication LevelAct as lead and main point of contact… more
- Merck & Co. (North Wales, PA)
- …Responsibilities: Responsible for the operational planning, feasibility, and execution of a clinical trial .May serve as the clinical trial team leadMay lead team ... planning, development, and execution elements (eg, data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates,… more
- Merck & Co. (Rahway, NJ)
- …across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, packaging and ... the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic and operational plans for all activities… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates strategic ... activities include, but are not limited to:-Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area representatives… more
- Merck & Co. (North Wales, PA)
- …for the operational planning, feasibility, execution and conduct of clinical trial (s).Serves as the Clinical Trial Team lead. Leads and ... subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.Liaises with partners, vendors, and vendor management team . Review… more
- Genmab (NJ)
- …indication lead for both early and late-stage programs, and/or as trial responsible statistician with responsibilities as described below. The Associate Director ... courses and perform professional networkingEngage with regulatory authorities on trial level discussionsArranges/attends lessons learned to share learningsRepresents Genmab… more
- Genmab (NJ)
- …integrity? At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our science through compelling clinical ... of regulatory submissions (eg, NDA, BLA, MAA).Drive collaboration with cross-functional trial teams to manage timelines, facilitate meetings, and lead review… more
- Clinical Dynamix, Inc. (Waltham, MA)
- …Reporting to the Sr. Director, Clinical Excellence Operations the Senior Manager /Associate Director, Records Management will be responsible for expertise, oversight, ... implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation.… more
- Merck & Co. (San Francisco, CA)
- …the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will streamline the execution of our Company's DSCS Digital Strategy to ... robustness across organizational deliverables.- In this role, the DSCS Digital Project Manager will provide tactical direction and partner with the DSCS Digital… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring integrity, consistency and adherence ... of at least one study are in scope.The Programming Manager will support the Data Management, Statistics, Drug Safety,...Practical knowledge and experience using R to support clinical trial analyses.For US based candidates, the proposed salary band… more
- Merck & Co. (North Wales, PA)
- …This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical ... study materials (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection in alignment… more
- Merck & Co. (Rahway, NJ)
- …chain across the full Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, packaging ... arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point of contact… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Manager Audits & Compliance, GCP/Document Audits supports end-to-end audit activities ... Document (CTD), Clinical Study Report (CSR) and Nonclinical Study Report (NCR), electronic Trial Master File (eTMF) and other pivotal documents to be submitted to… more
- Merck & Co. (Rahway, NJ)
- …This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation -of clinical ... (e . g . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with… more
- Genmab (NJ)
- …would love to have you join us!Responsibilities:Lead programmer for a trial (s)Review CRFs for adequacy and consistencySupport establishment and maintenance of Genmab ... SDTM and ADaM database standardsDrive development of programming specificationsDrive consistency across trialsResponsible for keeping proper documentation and filing to eTMFProvide sponsor oversight of vendor programming activitiesSupport in-house production… more
- American Oncology Network (Waycross, GA)
- …are rescheduled to accommodate physician's vacations, conferences, and personal appointments. Run trial close daily. Verify with office manager and fax to ... signature. Call funeral home when paperwork is completed. Run trial close each day. Fax appropriate information to the...labeled and filed correctly. Notifies Onco/EMR support or office manager to remove faxes that were filed incorrectly in… more
- Tennessee Oncology (Chattanooga, TN)
- …cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology's mission ... the patients we serve. Job Description: The Research Nurse Manager ensures the integrity and quality of clinical trials...that the integrity and quality of the clinical research trial is maintained and that the trial … more
- Profound Research (Las Vegas, NV)
- …Quality Role & Responsibilities: -Maintain site compliance for all clinical trial activities in accordance with established research protocols and standards in ... expectations. -Coordinate as primary CRC on at least one trial of medium to high complexity and serve as...are met for the respective sites. -In addition to trial specific responsibilities, support in building and implementing a… more
- ChampionX (Midland, TX)
- ChampionX has an immediate need for a Business Development Manager based in Midland, TX supporting our Reservoir Chemical Technologies team. If you are a passionate ... knowledge as well as the delivery of innovative processes and programs Support/lead trial of new technologies and proactively show initiative by bringing ideas and… more
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