- Merck & Co. (Rahway, NJ)
- …mentorship to other clinical scientists.Core Skills Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... 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… more
- Merck & Co. (Rahway, NJ)
- …tactical/scientific mentorship to other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP and ICH) ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this.... , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability ... 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… more
- Merck & Co. (North Wales, PA)
- …managing any study specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs.Facilitate operational meetings ... language in associated contractual templates. Ensures Good Pharmacovigilance Practice and regulatory compliance in such arrangements. Contribute to the management of… more
- Genmab (NJ)
- …Writing Manager to help us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart of a team that plays ... Global Medical Writing team, you will drive the development of high-quality clinical documents to support operational, medical, and regulatory activities across… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring integrity, consistency and adherence ... the programming efforts of at least one study are in scope.The Programming Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical … more
- Merck & Co. (North Wales, PA)
- …Vice President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and ... DescriptionIn Biostatistics and Research Decision Sciences (BARDS), a distinguished department within our renowned Research and Development division, quantitative… more
- BioAgilytix (San Diego, CA)
- … department staff.Develop and maintain SOPs in compliance with regulatory requirements.Drive innovation through evaluation and implementation of new analytical ... departments. This role oversees daily laboratory operations, scientific quality, and regulatory compliance across both functions, supervising up to 40 employees.The… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions ... contact with key account personnel, including C-suite executives and department heads. Additionally, this role maintains relationships with other...NNI, a self-starter who is self-led and keeps their manager up to date on progress and ensures no… more
- Johns Hopkins Medicine (Baltimore, MD)
- …NP or Physician Assistant) to lead the APPs in the Oncology, Inpatient, department . Reporting to the Director of Advanced Practice Providers for Oncology, this ... recruitment and training, and ensuring high-quality patient care across various clinical settings: inpatient units and intensive care units. Key Responsibilities:… more
- Johns Hopkins Medicine (Washington, DC)
- …pharmacists and health care practitioners. In collaboration with Director of Pharmacy, Clinical Operations Manager counterpart, Clinical Pharmacy Manager ... nursing inpatient services, as well as a 24-hour Emergency Department . Sibleys campus is also home to Grand Oaks,...processes and hazardous drug program to ensure compliance with regulatory standards (TJC, CMS, USP 797 and 800). Manages… more
- Eisai, Inc (Nutley, NJ)
- …speakers and related aspects of speaker programsCollaborate with Promotional Program Manager for speaker usage and issuesOffer feedback on nominating new speakers ... of brand plansStrong communication and presentation skillsUnderstanding of legal and regulatory issues impacting pharmaceutical product marketing as well as the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for ... technical and career, of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires strong knowledge about RBQM,… more
- Johns Hopkins Medicine (Baltimore, MD)
- …and qualifications.* Position Summary: Reports to the Division or Lab Directors, Lab Manager 2 OR the Department of Pathology Administrator. Responsible for the ... Hospital, Baltimore, MD-Core Laboratory Full Time/Days-8am-4:30pm *Will consider at Manager I or Manager II, depending on...management of a subset of laboratories within the Department of Pathology. Provides leadership to a small group… more
- The University of Miami (Miami, FL)
- …*Ability to lead, motivate, develop, and train others. DEPARTMENT ADDENDUM The Clinical Research Nurse Manager will be responsible for overseeing day-to-day ... the Career worklet, please review this tip sheet. The Department of Clinical Translational Research Site is...Translational Research Site is currently seeking a full time Manager , Clinical Research Nursing to work in… more
- Trinity Health (Boise, ID)
- … regulatory standards. Promotes effective and efficient utilization of clinical resources from admission to discharge. Initiates and presents "denial letters" ... cases, and desired patient outcomes. Introduces self to patient and family and explains clinical resource manager role and the process for patient and family to… more
- Veracity Solutions (Clackamas, OR)
- Manager , Department - Patient Care / Hospital Onsite Clackamas, OR Accountable for management of a patient care unit(s). Partners with healthcare team to assure ... patients and communities. Collaborates with nursing programs to provide required resources. * Clinical Practice: Acts as an expert resource for staff and utilizes… more
- NYULMC (New York, NY)
- …maintains responsibility for developing, implementing, and maintaining Quality Assurance for Clinical Laboratory. Oversees regulatory compliance for Clinical ... compliance and quality. Reports to Director of Quality & Regulatory for Clinical and Anatomic Pathology. Works...regulatory standards. Data: Oversees data compilation for the department as it relates to quality assurance. Compiles and… more
- Cedars Sinai (Los Angeles, CA)
- …of patients from around the world who receive treatment here each year. The Manager , MN Clinical Operations supports the safe and effective delivery of patient ... functionality and providing ongoing direction for system utilization. Assists the Senior Clinical Operations Manager in developing and managing the budget for… more
