- Merck & Co. (Rahway, NJ)
- Job DescriptionUnder the direction of the applicable management, the Lead Clinical Data Manager (LCDM) is responsible for executing end to end data management ... activities pertaining to clinical trials, including but not limited to: data management...and resource allocation. Supports the comprehensive development of junior staff and encourages effective interaction with business partners to… more
- Merck & Co. (Rahway, NJ)
- …independently, collaboratively as a member of a team, or successfully as a leader , with equal effectiveness.Interact with staff across multiple of our company's ... standards and associated processes for growth opportunitiesThe Vocabulary Specialist may lead or participate in:Internal clinical data standards forumsStandards… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, to ... drug products. Operational leadership of the FLEx complex is shared across two co- leader roles, and includes operations that support end-to-end GMP clinical … more
- Merck & Co. (Rahway, NJ)
- …quality standards and adverse event reporting requirements internally and externally.Our Clinical Research and Pharmacovigilance team push the boundaries of global ... healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and... and financial contracts within fair market value.Contribute or lead initiatives and projects adding value to the business,… more
- Merck & Co. (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D.- The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... statistical representative and core member in the Risk Management Safety Teams.- Lead and provide statistical support for related drug/vaccine projects in … more
- Merck & Co. (Rahway, NJ)
- …biostatistical support for related drug/vaccine projects in Late Development Statistics. Lead the interaction with Clinical , Regulatory, Statistical Programming, ... analysis.May lead a team of statisticians and statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating… more
- Merck & Co. (Rahway, NJ)
- …trial teams and in other trial-level development forums.Under the guidance of more senior staff , may serve as the data management lead or perform a support ... Participates in the development of, and ensures adherence to, our company's clinical data management procedures. Interacts with staff across sites, countries,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Our Research ... new milestones in global healthcare. Our company's Pharmaceutical Sciences & Clinical Supplies organization translates molecules to medicines, working from the… more
- Merck & Co. (North Wales, PA)
- …insight, knowledge of the therapeutic area, and scientific expertise, they will lead the development of comprehensive publication strategy and plans as well as ... scientific data dissemination. They work closely with both internal writing staff and medical communication agencies to efficiently allocate resources for writing,… more
- Merck & Co. (Rahway, NJ)
- …and coordinating statistical activities supporting drug/vaccine projects.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and our ... providing guidance to others in the statistical support for clinical drug/vaccine projects.-Interacts with Academic Research Organization (ARO), Contract Research… more
- Merck & Co. (Rahway, NJ)
- …requirements.May lead a team of statisticians and statistical programming staff to ensure that all programs meet analysis requirements, internal standard ... in research activities for innovative statistical methods and applications in clinical trial development.-Mentors and guides junior staff in functional… more
- Merck & Co. (North Wales, PA)
- …activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …and world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes creation and validation of ... external stakeholders including Statistical Programming, Statistics, Regulatory, Data Management, Clinical and other project stakeholders.-Primary ResponsibilitiesSupporting project teams in… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Catalent (Philadelphia, PA)
- …located in the Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical ... be accessible to production floor, supply chain and office staff and to use required office equipment. Specific vision...Time Off accrual Medical, dental and vision benefits effective day one of employment Tuition Reimbursement - Let us… more
- Merck & Co. (Rahway, NJ)
- …achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing ... Research & Manufacturing, in a fast-paced, multidisciplinary environmentParticipate in or lead 1) development of robust and scalable upstream processes for biologics… more
- Merck & Co. (Rahway, NJ)
- …and vaccine programs.Interact with cross functional scientists including, Statistics, Clinical , Regulatory, QP2, CSRM, Data Management and Statistical Programming to ... plan for the statistical analysis and reporting of clinical drug and vaccine projects.Set direction for the analysis and reporting deliverables.Negotiate and… more
- Merck & Co. (Rahway, NJ)
- …Senior Specialist - Manufacturing Automation position will report to the Director, Engineering, Automation Lead position and will be a member of the EF Team at the ... (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The… more
- Catalent (Harman, WV)
- …needed. The Role Provides strategic direction to the QA Systems staff supporting Investigation/Deviation/ CAPA Management, Change Control, Risk Management, Quality ... effective teams and foster a culture of employee engagement and motivation. Ensure staff are fully trained on all cGMP manufacturing operations and documentation and… more
- Merck & Co. (Rahway, NJ)
- …SM PR&D pipeline. Responsibilities: Under the scientific direction of a facility lead , the Operations Specialist will participate in equipment setups, raw material ... aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of… more
