- Integrated Resources, Inc (New York, NY)
- Job Title: Credentialing Specialist Location: New York, NY, 10004 Job Duration: 3months with possible extension Shift Time: 9am to 5pm 5 days a week. Pay Range: ... aspects of provider credentialing and re-credentialing. Duties: . The Credentialing Specialist is responsible for facilitating all aspects of provider credentialing,… more
- ProKatchers (Bowling Green, NY)
- …offices to ensure timely completion of duties to meet internal and regulatory standards and requirements. Perform clinical audits via EMR, in-house paper medical ... records, on-site provider visits to measure compliance with preventive health guidelines and to measure effectiveness of quality improvement initiatives. Identify, track and report variation from standards of care by audit of core operations, patient care… more
- Merck & Co. (Rahway, NJ)
- …DescriptionWe are seeking a Growth and Improvement minded Stability Sample Management Specialist - Analytical Chemistry that can help drive our Strategic Operating ... and Compliance group has an exciting opportunity for Stability Sample Management Specialist . We are searching a highly talented and motivated individual to serve… more
- Merck & Co. (Rahway, NJ)
- …auditing and Quality Risk Management.As required, participate in Regulatory Agency inspection activities.Deliver stewardship for company's corporate initiatives ... with end-to-end data governance.Expertise with configuration management.Knowledge of published regulatory agency data integrity, computer software assurance guidance.Moderate level… more
- Rose International (Jersey City, NJ)
- …Hiring Organization: Rose International Position Number: 463644 Job Title: Transformation Specialist PM Job Location: Jersey City, NJ, USA, 07395 Work Model: ... lengthened based upon a client's business needs and requirements. ** The Transformation Specialist Project Manager will be a key member of the Procurement and… more
- Spectraforce Technologies Inc (Bridgewater, NJ)
- Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ HOUR ... have experience with CTD (Common Technical Document) modules. Will complete regulatory submissions, compliance, and amendments. Expert in Microsoft Office (Word,… more
- Eisai, Inc (Nutley, NJ)
- …mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... sales/business analytics, etc.)Strong understanding of pharmaceutical manufacturer compliance & regulatory requirementsDemonstrated success in driving growth and profitability, establishing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …global function on study and project teamsProduces independent writing for publications and regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... function on study and project teams, and participate in and contribute to regulatory and KOL meetings. This position requires significant understanding of PK-PD and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …global function on study and project teamsProduces independent writing for publications & regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (Rahway, NJ)
- …Operations Equipment Operation Engineer will serve as a primary operations specialist within in the FLEx Sterile GMP Clinical Manufacturing facility.To enable ... to contribute to equipment and facility design, system commissioning/qualification, regulatory certification, as well as other workstreams' critical activities to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The...handle corrective and preventative action records. Supports internal and regulatory audits. Requirements A minimum of a Bachelor's degree… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to be part of the team responsible for Warehouse activities that will… more
- Integrated Resources, Inc (Warren, NJ)
- Job Title: Validation Specialist Job Location: Warren, NJ Job Duration: 5 Months Work Schedule: Mon - Fri, Business Hours Job Description: The Validation ... Specialist , Computerized Systems, is responsible for performing initial and...decision making skills. . Knowledge of validation industry and regulatory requirements. . Ability to work independently and participate… more
- Penske Truck Leasing Co., LP (Queens, NY)
- …least 3 years of experience in a Human Resources role (generalist, specialist , recruiting) required, or relevant field operations experience will be considered for ... preferred (ie, PHR, SHRM-CP). * Some knowledge of employment law and regulatory compliance issues preferred (additional knowledge may be required in certain states,… more
- Fidelity TalentSource LLC (Paramus, NJ)
- …Representative to have rewarding interactions with clients. As a subject matter specialist in compliance and all front lobby transactions, you will partner and ... includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). These investigations… more
- Creative Financial Staffing (Stamford, CT)
- …portal submissions, and act as a proficient backup for the Payroll Specialist . Conduct comprehensive State and Federal Tax reporting, meticulously audit and ... maintain data integrity across multiple states, ensuring consistency and compliance with regulatory requirements. Contribute to the upkeep of the ERP system and… more
- Actalent (Hackensack, NJ)
- Description: The Regulatory Specialist is responsible for promoting compliance with Federal Regulations, Good Clinical Practice (GCP) and Institutional policies. ... The Regulatory Specialist will serve as liaison to investigators, collaborating divisions, departments and institutions, the Institutional Review Board (IRB) and… more
- Eaton Corporation (Long Branch, NJ)
- Eaton's ES EMEA CS LS division is currently seeking a Regulatory Specialist . This role is based out of our Sarasota, FL OR Long Branch, NJ facilities. The ... Regulatory Specialist will be responsible for developing, maintaining, and executing product certifications for new and existing products. This individual will… more
- J&J Family of Companies (Raritan, NJ)
- Senior Regulatory Affairs Specialist (Robotics & Digital Solutions) - Ethicon, Inc. - 2406181478W **Description** Robotics & Digital Solutions, part of the ... Johnson & Johnson Medtech Surgery, is recruiting for a **Senior Regulatory Affairs Specialist ** _. The preferred location for this role is within a commutable… more
