Provider Contracting Director is responsible for the operations of the provider contracts department. Ensures that provider contracts are processed to support accurate and efficient claims payments. Being a Provider Contracting Director oversees the formulation of provider contracts and specific terms. Analyzes contract data and provides financial projections. Additionally, Provider Contracting Director requires a bachelor's degree. Typically reports to top management. The Provider Contracting Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. To be a Provider Contracting Director typically requires 3+ years of managerial experience. (Copyright 2024 Salary.com)
Optima Research Center Seeks Clinical Research Nurse Practitioner (Sub-Investigator) in Macedonia, OH
Position Details:
The Clinical Research Nurse Practitioner (CRNP) is a master’s prepared independently licensed nurse who functions as a sub-investigator for clinical trials conducted by Optima Research as part of a multidisciplinary patient care team. The CRNP provides medical evaluation, care, and treatment of clinical research subjects in compliance with study protocols. This activity is performed in collaboration with the Principal Investigator(s) and the Director of Clinical Research. The CRNP is required to have knowledge of protocol design and Good Clinical Practices (GCP) as set forth by the Federal Regulations and International Conference of Harmonization (ICH) Guidelines for the protection of human subjects and the conduct of clinical research required. The CRNP ensures protocol compliance, Investigational Article accountability, and proper follow-up during the clinical trial.
Essential Sub-Investigator Functions:
The Clinical Research Nurse Practitioner is responsible for the following essential sub-investigator functions:
Pre-Study
During Study
Post-Study
Additional Functions and Responsibilities:
Requirements:
Qualifications:
About The Indiana Clinical Trials Center / Optima Research:
The Indiana Clinical Trials Center (ICTC) is a comprehensive and highly experienced clinical research site and Trial Management Organization (TMO). Optima Research is a successful extension of The Indiana Clinical Trials Center. Our research centers focus primarily on Phase I – IV dermatologic clinical trials.
For patients struggling with difficult, complex, and often chronic conditions, ICTC/Optima Research allows them to participate in cutting-edge research that can help them overcome and improve their situations. In enrolling such patients at high levels, we always conduct such clinical trials under the guidelines of Good Clinical Practice (GCP).
For sponsors, we pride ourselves on enrolling appropriate patients at high levels. In addition and more importantly, we promise to provide our sponsors with outstanding, complete, detailed data for each of their studies.
Ultimately and at all times, our patient's safety and best interests are of utmost importance to us.
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0 Provider Contracting Director jobs found in Cleveland, OH area