In this role, you will be responsible for global IT technical strategy development for the Consumer Regulatory, Medical, Clinical, Toxicology, Human and Consumer Use Testing groups, as well as the Diabetes and Vision Care businesses of Consumer Medical Device.
The Local Study Manager is responsible for planning, executing and reporting on a number of phase II-III and global phase IV clinical studies for the planning and site feasibility through study close-out, in compliance with Novartis processes and regulatory requirements.
The Manager, Clinical Quality Assessment (CQA) Auditor is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Manager, CQA Auditors mission and responsibilities, the audits and activities require proven ability to independently interact with all internal (e.g. Projects Teams, Trial Operations) and external (e.g. Vendors / CRO) operational staff involved in the audited clinical research activities.
In this role, you will be responsible for the direct functional management of a group of Local Trials Managers ( LTMs ), and Site Managers ( SMs ) in the Neuroscience and/or Immunology Therapeutic Areas within Global Clinical Operations ( GCO ).
This position is responsible for working closely with the heads of the four Clinical Business Lines, as well as interfacing with Commercial functional teams (e.g. Consulting) and agency partners to develop and implement strategic marketing initiatives to support existing and new service offerings of the Clinical Division. Moreover, the Senior Marketing Manager serves as an internal brand champion.
In this role, you will be responsible to develops and maintains effective relationships through effective and timely communication. Responsible for driving the fms culture through values and customer service standards.
In this role, you will be responsible for development, management, maintenance of study deliverables [i.e. timelines, study plans, etc.] through collaboration with internal and external stakeholders using data and strong inter-personal influencing skills to make robust data driven decisions.
In this role, you will managing the clinical study timelines, deliverables and risks, working with the client and Business Services to finalize the project budget and scope, serving as primary contact with client to ensure appropriate communication, managing project budget, and participate in internal and external meetings.
In this role, you will develop and/or oversee development of other project-related documents including protocols, case report forms, study manuals, informed consent forms, monitoring plans, communication plans, tracking tools, and other project tools as needed.
In this role, the selected candidate will develop and maintain standards for database design by defining standard database modules, variable names, attributes, and associated data validation/logical checks and also work closely with data management function to define and maintain standard on-line data validation/logical checks as well as additional batch validation/logical checks.
In this role, you will be responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access, Investigator Initiated, registries and Compassionate Use) under the leadership of the CTH.
In this role, you will provide leadership, management, planning and mentoring for a diverse, field-based, clinical workforce of Nurse Practitioners, Registered Nurses, Health Coaches, Licensed Practical Nurses, Social Workers, Preceptors and Team Leaders, who are collectively responsible for achieving client and clinical objectives within a defined geography.
The Senior Project Manager will lead the cross functional project teams including clinical operations, data management, biostatistics, medical writing and clinical QA, to ensure quality, on-time and within budget deliverables for primarily Phase II-IV clinical trials.
In this role, you will plan, directs, and supports both clinical and administrative staff to ensure that they provide mental health services to an adult mental health population in the community on a 24/7 hours basis. Assures departmental goals and/or objectives are accomplished within prescribed time frame by performing the job responsibilities personally or through subordinate staff.
As a clinical supervisor of our hemodialysis team, the natural leader we select will provide direction, inspiration, and counseling to staff members, and coordinate all aspects of care, from admission to discharge. In addition, this individual will hire, train, lead a team, and ensure quality control and compliance with laws and regulations.
This position is responsible for increasing the bandwidth and velocity of Health Affairs/HNJH Clinical Operations Department. This role will facilitate the development, coordination, communication, and accomplishment of short and long-term business strategies.