- 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 and regulatory documents. You'll be at the heart...to grow with us.As part of our Global Medical Writing team, you will drive the development of high-quality… more
- Merck & Co. (Rahway, NJ)
- …and/or epidemiologists within BARDS, as well as stakeholders in data management, medical writing , and clinical operations to gather and document requirements for ... under the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other programming colleagues and biostatisticians… more
- Merck & Co. (North Wales, PA)
- …SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position, you will have the ... cross functional team.Job ResponsibilitiesResponsible for leading specific aspects of clinical /scientific execution of clinical protocol(s). This may… more
- Merck & Co. (Rahway, NJ)
- …- This position leads the scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this position, you will have the ... team . - Job Responsibilities - Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s) . This may include: Serving as… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming ... for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS program development for… more
- Eisai, Inc (Nutley, NJ)
- …and for-cause audits Knowledge of data integrity controls and systems quality for clinical area Strong analytical skills and report writing skills Experience ... your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality...you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for design, delivery… more
- Merck & Co. (South San Francisco, CA)
- …DescriptionBrief Description of PositionTranslational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration ... with Immunology Discovery Sciences and late-stage Immunology Clinical Research. We work with all therapeutic areas within our Research Division with the role focused… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Overview - Basic Functions & Responsibility The Global Clinical Supply (GCS) organization is within our Research and Development division ... and is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development division...Sense, Power BI, ThoughtSpot is a plus).Strong expertise in writing and optimizing SQL queries for data extraction and… more
- Merck & Co. (North Wales, PA)
- …DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have ... management, communication, and collaboration skills in support of our clinical trials.Job Responsibilities: Responsible for the operational planning, feasibility,… more
- Merck & Co. (South San Francisco, CA)
- …strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The successful candidate will have an essential strategic ... strategies and interact with various stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role… more
- Merck & Co. (South San Francisco, CA)
- …of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist with a proven ... 5-year experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as Dermatology,… more
- Merck & Co. (Rahway, NJ)
- …for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards ... and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be… more
- Merck & Co. (Rahway, NJ)
- …review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release, and maintenance in support of ... our company's clinical supply programs. This person will also independently review and approve documentation accompanying the disposition of API materials to ensure… more
- Merck & Co. (Rahway, NJ)
- …Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation and filling ... of clinical and developmental supplies for sterile products, including critical program needs related to new products undergoing process development, new products… more
- Merck & Co. (North Wales, PA)
- …the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your ... management, communication, and collaboration skills in support of our clinical trials.Job ResponsibilitiesResponsible for the operational planning, feasibility, execution… more
- Merck & Co. (Rahway, NJ)
- …& Development team that designs and develops benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug ... using semi-automated and automated equipment, conduct functional testing, assist in clinical batch manufacture as an equipment subject matter expert, assist with… more
- Merck & Co. (Rahway, NJ)
- …opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions, ... will preferably have experience with high concentration biologics to support clinical and commercial development. Maintaining a strong network internally and across… more
- Merck & Co. (Rahway, NJ)
- …a ms of experienced sci e ntis ts to discover and advance the clinical development of novel small molecules, biologics, and vaccines for infectious diseases. The ... Responsibilities: Represent QP2 on infectious disease and vaccine discovery, early clinical development and late clinical development teams, leveraging… more
- Genmab (NJ)
- …Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and ... writing corresponding SAS or other programs. The Senior Programming...of data consistenciesSupports specification and pooling of data across clinical trials within the same project.Supports in-house production of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport audit ... program for clinical studies and vendors as applicable for the area...development through Phase III and Pharmacovigilance studies preferredMedical, technical writing experience a plus Travel Ability Must have the… more
