- 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
- Bristol Myers Squibb (Trenton, NJ)
- …RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director Clinical Site Operations provides strategic oversight, ... leadership and management of clinical trial execution, including oversight of site management...and other applicable federal (FDA) and state regulations. The Associate Director Clinical Site Operations… 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
- System One (Plainsboro, NJ)
- Senior Clinical Research Associate - Regional Location: Home Based, Philadelphia, PA Area Type: Full time Start Date: ASAP Are you an experienced Clinical ... sites in a risk-based monitoring model. Responsibilities: + Responsible for providing site management and support to external trial staff (Principal… more
- Merck (Trenton, NJ)
- …The position will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area, to proactively ... and maintain GCP inspection procedures and guidelines within Global Clinical Trial Operations (GCTO). + Contribute to...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… 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)
- …members including clinical directors and study managers to lead/support clinical trial scientific activities. **Job Responsibilities** + Responsible for the ... clinical protocol(s). + Serves as the lead clinical scientist on the clinical trial...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… 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
- 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
- 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
- Merck (West Point, PA)
- …space. The team lead will be responsible to read, comprehend, and translate clinical trial protocols /packaging specifications into clinical label generation ... software. The team lead will design clinical supplies trial labels for primary, secondary,...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… 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
- Merck (West Point, PA)
- … pharmacology, biomarkers of target engagement, experimental medicine platforms, early clinical trial designs and conduct, and operational understanding for ... **Job Description** The Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational...strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The AVP provides strategic oversight for the… more