- Merck (Trenton, NJ)
- …This role is accountable for execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations, ... Clinical Research, the individual is responsible to manage/oversee a team of CTCs( Clinical Trial Coordinator). As line manager the role is critical to… more
- Novo Nordisk (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... identification and mitigation planning for assigned clinical trial sites + Drives and tracks site ...tracks site activation and start-up activities with clinical trial sites to support trial… more
- Taiho Oncology (Princeton, NJ)
- …of timelines, budget, recruitment and country/ site selection strategies, and provision of clinical trial materials. + Serves as main study contact for the ... Associate Director, Clinical Operations Pleasanton, CA,...sites. + Responsible for the financial management of the clinical trial in conjunction with his/her supervisor… more
- Merck (Trenton, NJ)
- **Job Description** With support of Sr CRA ( Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager throughout all ... of site relationships through all phases of the trial . + Performs clinical study site management/monitoring activities in compliance with ICH-GCP,… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** **Specialist, Clinical Operations** Global Clinical Trial Operations (GCTO) is a global organization operating ... proportion of the GCTO budget, staff and deliverables. Global Site Agreements (GSA) is an organization within GCTO that...basis in support of our company's research development and clinical trial portfolio. We are responsible for… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Merck (North Wales, PA)
- …may be responsible for but not limited to: **Job Responsibilities** + Maintain clinical trial files (including eTMF), project processes, tracking systems, and ... internal and external stakeholders (eg, study sites, committees) in support of clinical trial objectives **Core Skills** + Pharmaceutical, research, medical,… more
- Novo Nordisk (Plainsboro, NJ)
- … deliverables across NACD. This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that ... US and CA warehouses operations for US and CA Clinical Trial sites. Accountable for overall performance...projects for NACD & Novo Nordisk (eg Investigators and site staff, vendors etc.). Establish and manage senior level… more
- Merck (North Wales, PA)
- …stakeholders including the Global Project Manager, Alliance Manager, Global Trial Manager, Clinical Sub Team, Clinical Trial Team, Outsourced Trial ... and improve lives. **Position Description:** Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist… more
- Bristol Myers Squibb (Princeton, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming. A ssociate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- Bristol Myers Squibb (Trenton, NJ)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge ... insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on...in their geography + Ensures FM team's execution of clinical trial support activities (as per established… more
- Bristol Myers Squibb (Trenton, NJ)
- …aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more
- Merck (North Wales, PA)
- …minimum of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. + MS (preferred) in Computer Science, Statistics, ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. **Required Experience and Skills:** + Experience leading… more
- Merck (North Wales, PA)
- …on a global basis. We are responsible for negotiating industry sponsored clinical trial agreements, confidentiality agreements, and other type of agreements ... the delivery of our company's diverse development portfolio comprising over 200 clinical trials in compliance with global and local regulations. The Regional… more
- Bristol Myers Squibb (Princeton, NJ)
- …management within a specific therapeutic area(s) and is accountable to manage clinical trial vendor partnerships that supports alliance and outsourcing ... management across multiple service categories of clinical trial activities in R&D. Key Responsibilities...out the highest potential of each of our colleagues. **On- site Protocol** BMS has a diverse occupancy structure that… more
- Merck (North Wales, PA)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics, Applied Mathematics, ... 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck (Trenton, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Bristol Myers Squibb (Princeton, NJ)
- …in partnership with cross-functional Business Process Owners (eg Biostatistics, Regulatory, Clinical Development, Safety and Clinical Trial operations). ... achieve drug development objectives to improve quality, capacity (productivity), and urgency ( clinical trial cycle times), while cultivating a foundational end… more
- Merck (Trenton, NJ)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas....seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
- Virtua Health (Marlton, NJ)
- …as required by protocol to ensure the submission of accurate information to clinical trial sponsors and regulatory agencies.* Responsible for submitting all ... Marlton, NJ Additional Locations: Job Information: Summary:Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a… more