Case Reviewer Salary at Coram Llc BETA

Must attend a compliance training to an advanced level. We send our 21-25 year old into our customer stores or restaurant locations once or twice each month to conduct mock purchases of cigarettes, tobacco vape products and / or liquor. Requirements: MUST be between ages 21-25!!!!! Also have their own source of transportation To apply for this position, click the link below or contact the local office at (312) 488-2928

Overview: The Disease Specific Care Reviewer-Ortho is responsible to review the following certification programs-Total Hip Replacement, Total Knee Replacement, Spine, Total Shoulder Replacement, Total Ankle Replacement, Hip Fracture and the Advanced Total Joint Replacement Program. Reviewers are expected to be knowledgeable regarding best practice in Orthopedics and provide our partner organizations with reviews that are educational and inspirational. The goal of certification is to ensure that patients are provided evidence-based orthopedic care and that the program continually monitors its performance of that care. Qualifications: Advanced Degree in Nursing or Licensure as a Physician required. Board Certification in Orthopedics required. Five years active experience in Orthopedics. Involvement in or familiarity with the Disease Specific Care Certification programs for Orthopedics All positions require 100% nationwide travel. Please review the following employment statuses. We are cu

The Senior Manager/ Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with p Medical, Business Partner, Communications, Healthcare, Staffing, Dance

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. The Senior Pharmacovigilance (PV) Specialist, Case Processing is primarily responsible for peer review of cases within the Case Processing team. The Senior PV Specialist performs initial case-level assessment of expectedne

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description Evaluates clinical service requests made by an organization's members and providers. Uses clinical judgment in conjunction with organization's criteria to adjudicate these requests. Provides clinical leadership in other areas of the organization. Identifies opportunities to manage members' clinical situations with a view toward creative problem solving and anticipation of possible future clinical problems for the member. Participates in the process to evaluate clinical service requests. Practices anticipatory case management for members whose cases come for review, in partnership with case managers. Participates in the Physician Review Units' appeal process of service denials. Participates in the development of Physician Review Units' policies and procedures. Actively participates in all unit continuous quality improvement activities. Our Client Our client is a fast-grow

The Process Review Evaluator is responsible for executing plans and projects to improve the efficiency and safety of operations. Duties include: conducting regular inspections and process audits, implementing control and sustainment plans, and training employees in a three shift operation to ensure standards are being met in all areas of food service and logistics. RESPONSIBILITY LEVEL: Implements strategies to achieve the goals for the organization and Great Lakes process review of Galley operations. Implements, revises, and sustains policies, procedures and programs. Typically works on projects and initiatives that span 3 - 12 months. PRINCIPAL DUTIES: 1. Project and Change Management: Effectively plans and manages own work to reliably complete routine job responsibilities and special assignments. May serve as a team member or subject matter expert on formal projects or within the department. Effectively engages in change affecting her/him, communicating appropriately with supervisor

Description Home Search Jobs Job Description Medical Reviewer/Safety Reviewer III (Remote) Contract: North Chicago, Illinois, US Salary Range: 40.00 - 43.00 | Per Hour Job Code: 360289 End Date: 2025-04-24 Days Left: 7 days, 3 hours left Apply To discuss more about this job opportunity, please reach out to Himanshu Kumar Singh(LinkedIn URL - https://www.linkedin.com/in/himanshu-kumar-singh-57b782258/ ) , email your updated resume at Email - himanshu.ksingh@collabera.com or give me a call at (425) 403-0902. Thank you! Pay Range: $40 - $43/hour Position Details: Industry: Pharmaceutical Job Title: Medical Reviewer/Safety Reviewer III (Remote) Location: Remote Duration: 12 months [+ Possibilities of extension] Responsibilities: Responsible for: medical review of promotional and non-promotional materials across multiple indications for one product Maintains expert understanding of product knowledge and labeling, associated disease states, relevant literature, treatment guidelines, competit

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $39.00 - 51.65 per hour work hours: 9 to 5 education: Bachelors responsibilities: Conduct MLR (Medical, Legal, Regulatory) review of promotional materials to ensure compliance with i