- Genmab (Trenton, NJ)
- …regarding Genmab's solid tumor therapies and relevant studies Provides US market input to Global clinical development and Global Medical Affairs ... be the subject matter expert responsible for leading the development and execution of the USMA strategic and tactical...with colleagues in other functional areas Ensures optimal safety, clinical oversight and highest quality standards are… more
- Genmab (Mercerville, NJ)
- …understanding of drug development including regulatory requirements and quality standards applicable to nonclinical and clinical laboratories (eg, GLP, GCP, ... highly skilled Senior Contract Manager specializing in nonclinical and clinical lab and data services to join our team...Furthermore, this role will take part in the further development of the global outsourcing, contract management… more
- Genmab (Yardley, PA)
- …head & neck cancer is preferred. 7+ years of medical affairs or clinical development background in oncology Biotech / Pharmaceutical industry experience, with ... Lead (MASL) the Director will be responsible for the development and execution of the Global Medical...trusted partnerships A strong ability to interpret and articulate clinical /HEOR data and the impact on development … more
- Genmab (Morrisville, PA)
- …The Role The successful candidate will contribute to the mission of the global data engineering function and be responsible for many aspects of data including ... creation of data-as-a-product, architecture, access, classification, standards , integration, and pipelines. Although your role will involve a diverse set of… more
- Genmab (Princeton, NJ)
- …the entire spectrum of drug development at Genmab, from Discovery to Late Clinical Development and beyond. The Head of Clinical Pharmacology & ... CPQS in the Translational and Quantitative Sciences Leadership Team and lead strategic development of pre- clinical and clinical pharmacology strategies for… more
- Genmab (Princeton, NJ)
- …the employee may represent Clinical Operations in Project Boards, Global Development Teams and Operational Committee's/Steering Committee's with the ... programs. The employee is responsible for establishing standard processes, templates and clinical standards to ensure the quality and timelines of regulatory… more
- Merck (North Wales, PA)
- …Acting as Global SME for assigned topics and SOPs, the Global Clinical Development (GCD) Standards & Training Lead (STL) will work closely with ... Global Clinical Trial Operations (GCTO), and Global Clinical Development (GCD) leaders,...and understanding of end-to-end drug development and clinical trial processes, including related standards and… more
- Taiho Oncology (Princeton, NJ)
- …leads and manages multiple complex global studies to support the Clinical Development Plan. The Associate Director (AD) is responsible for ensuring ... and training according to trial specific requirements and industry standards . + Verifies that the investigator follows the approved...on global product level teams to support clinical development plan strategy and provides timelines… more
- Taiho Oncology (Princeton, NJ)
- …minimal supervision, leads and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ... ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other… more
- Merck (West Point, PA)
- …job aids/SOPs and participates in or leads cross-functional teams to develop global clinical development procedures. Identifies and communicates best ... Applies thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development . Represents Early Stage Development on early… more
- J&J Family of Companies (Skillman, NJ)
- …Health Clinical Research and Claims team dedicated to the development and implementation of skin measurement and visualization techniques for scientific support. ... Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse...Director and fulfill the responsibilities for this role on clinical studies + Participate in the development … more
- Merck (North Wales, PA)
- **Job Description** Clinical Development heavily relies on accurate data collected from patients who are part of Clinical Trials. Trial Standards , Trial ... first site ready. + Remove obstacles and enable the Global Clinical Trial Organization to focus on...Organization to focus on what matters. As Research and Development IT continues the transition from project / portfolio-based… more
- J&J Family of Companies (Trenton, NJ)
- …be a member of the Global Medical Affairs team, leading the conduct of a global clinical study using the portfolio of compounds at Janssen with the aim of ... clinical research and the highest personal and ethical standards . Experience in running and the conduct of global or highly complex studies is a key area of… more
- J&J Family of Companies (Trenton, NJ)
- …all system deliverables associated with clinical systems; + Support the development and maintenance of global harmonized processes and procedures for system ... anywhere is united states. Biosense Webster, Inc. is the global leader in the science of diagnosing and treating...provide oversight and coordination of all aspects of the development and management of clinical study databases… more
- Merck (North Wales, PA)
- …among the intellectually curious, join us-and start making your impact today. **Overview:** Global Clinical Trail Operations (GCTO) is a global organization ... responsible and accountable for the execution of the Merck clinical research portfolio. The Global Clinical...Operations . Exposure to Senior level positions within the clinical development . Hands-on experience in the… more
- Sedgwick (Trenton, NJ)
- …in establishing policy and procedures to assure compliance to best practices, clinical management services standards , state regulations, and client service ... Place to Work(R) Most Loved Workplace(R) Forbes Best-in-State Employer Clinical Manager **This manager will have to be able... staff. + Promotes and adheres to all URAC standards and assures compliance to maintain successful URAC certification.… more
- Wolters Kluwer (Trenton, NJ)
- …our advanced clinical decision support solutions meet the highest quality standards , which are of paramount importance to the company's mission to improve the ... (eg, RxNorm, SNOMED, ICD-10-CM, etc.). In addition, you will possess proven clinical and analytical skills as well as the ability to work collaboratively… more
- J&J Family of Companies (Trenton, NJ)
- Sr Clinical Account Specialist - New Jersey - Biosense Webster Inc. - 2406196923W **Description** Johnson & Johnson is recruiting for Sr Clinical Account ... from AFIB each year. Biosense Webster, Inc. is the global leader in the science of diagnosing and treating...The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the development ... labeling content and strategy of assigned product(s) in various stages of drug development , which may include products of medium complexity and updates to TLP, CCDS,… more
- Sedgwick (Trenton, NJ)
- …+ Establishes policy and procedures to assure compliance to best practices, clinical operations service standards , state regulations, and client service ... to Work(R) Most Loved Workplace(R) Forbes Best-in-State Employer VP Clinical Operations Join us in leading, advancing, and executing...+ Be a part of a rapidly growing, industry-leading global company known for its excellence and customer service.… more
