In this role, the Clinical Programs Nurse Administrator will have overall responsibilities to administer the Quality and Practice Incentive Programs and to act as liaison to a clinical and provider base of 100 individuals.
This position assists the Clinical Director in directing the preparation and maintenance of patients clinical record, including safe, quality and competent care of the pre - operative and post- operative care of all patients
In this role, you will ensure that the study is conducted and reported according to legal requirements, relevant regulatory standard (e.G. Gcp, glp) and the applicable internal policies and procedures.
The Senior Manager of Clinical Outsourcing will focus on OPDC Clinical Contracting responsible for supporting OPDC Clinical Regulatory Teams (CRT) in selecting, negotiating costs, contracting and providing business oversight of CROs and other ancillary vendors.
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.
Utilizing knowledge and proficiency in the Lean Six Sigma system, collaborates with stakeholders to identify and define problems pertaining to inefficiencies and to eliminate waste within the division facilities and programs.
In this role, the selected candidate will support inspections by regulatory agencies by assisting in the organization of and preparation for, coordination, hosting, conduct, documentation and follow-up of regulatory inspections.
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.
The Clinical trial manager should have critical thinking skills for problem solving and have the lateral and strategic thinking capacity to drive the study(ies) and understanding the upstream, downstream and lateral implications of decisions that affect study outcomes and timelines.
Responsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned.