About Level2 Level2 is a healthcare start-up that is building the next generation of virtual care for individuals with chronic conditions including Type 2 diabetes. This new business is dedicated to empowering patients to manage and achieve remission of their condition through an end-to-end vi...
North American Science Associates (NAMSA) started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976, thus pioneering the industry. NAMSA was the first independent company in the world to focus solely on medical device materials for safety. ...
Description: Providence St. Joseph Health is calling an Insurance Verification and Authorization Specialist to our location in Portland, OR. We are seeking an Insurance Verification and Authorization Specialist to be responsible for securing appropriate patient account reimbursement by obtai...
Careers that Change Lives In this exciting role as a member of Corporate Clinical Quality & Compliance, the Senior Clinical Quality Specialist (CQS) will be responsible for completing audits and ensuring that clinical personnel across Medtronic are operating within U.S. and international regulator...
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting...
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting...
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting...
SUMMARY: The Senior Specialist, Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle. RESPONSIBILITIES: Liaise with the Regulatory Affairs Manager/Regulatory Affairs Director to plan, organise, compile progres...
Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11)Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical educa...
Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11) Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical...
Job DescriptionAs Compliance Specialist in the Regulatory Compliance Team in the US you will be responsible for market analyses and regulatory license applications for new regulated markets as well as maintaining our existing licenses along with providing support to various stakeholders in relation ...
About StrykerStryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and ho...
Kelly Science & Clinical is currently seeking a Remote Regulatory Affairs Senior Specialist for a long-term engagement with one of our Global Med Device clients out of Raynham, MA***This role is fully remote*** This person will join our Kelly FSP (Functional Service Provider) division, a ma...
Responsibilities: Evaluate the regulatory environment and provide internal advice throughout the product lifecycle for marketed devices to ensure product compliance. Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develops solutions. Assist in the develo...
In this role, you have the opportunity to Provide Regulatory support the company's Emergency Care and Resuscitation business products. With advance expertise and knowledge of regulatory requirements you’ll developed and drive regulatory strategies for high tech medical devices. You are responsible ...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us an...
SUMMARY: The Principal Specialist, Site Contracts is responsible for providing senior oversight and expertise to all site contracts activities during all stages of a Clinical Trial including the development of investigator grants, Clinical Trial Agreement templates and applicable plans, negoti...
Job Description The Digital Financial Crimes Risk Analyst is critical in supporting the Digital business line’s FCC risk oversight program. A successful candidate will have a demonstrated ability to independently lead and coordinate FCC first line of defense (1LOD) oversight, including pre-productio...
Job Description The Digital Financial Crimes Risk Analyst is critical in supporting the Digital business line’s FCC risk oversight program. A successful candidate will have a demonstrated ability to independently lead and coordinate FCC first line of defense (1LOD) oversight, including pre-productio...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us and...
Enterprise Bank & Trust was founded in the spirit of entrepreneurship and community. From the small mom-and-pop coffee shop to the large construction company that employs local people, our goal is to help businesses succeed and our communities thrive. With offices in St. Louis, Kansas City, Phoenix,...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us an...
Summary: Reports to the Manager of Hospital Coding for Lifespan Corporate Services.Under general supervision and within Hospital and departmental policy ensures accurate coding and data quality creates consistency and efficiency in inpatient services through ongoing performance of ICD-10-CM and I...
About Level2 Level2 is a healthcare start-up that is building the next generation of virtual care for individuals with chronic conditions including Type 2 diabetes. This new business is dedicated to empowering patients to manage and achieve remission of their condition through an end-to-end virtual ...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us and...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us and...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
At Cepheid, we are passionate about improving health care through faster, more accurate diagnostic tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us, every mom...
Do you have compassion and a passion to help others? Transforming healthcare and millions of lives as a result starts with the values you embrace and the passion you bring to achieve your life’s best work.(sm) Positions in this function are responsible for the development and/or on-going managem...
About StrykerStryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital...
UnitedHealthcare is a company that's on the rise. We're expanding in multiple directions, across borders and, most of all, in the way we think. Here, innovation isn't about another gadget, it's about transforming the health care industry. Ready to make a difference? Make yourself at home with us an...
Everi is looking for a regulatory compliance licensing specialist to join our growing team! If you are a go-getter and thrive at attention to detail, we want to speak to you! In this position, you will process occupational licensing applications. - - This role is local to Las Vegas with the option t...
Senior Director, Clinical Biomarkers - Permanent - RemoteProclinical Staffing is seeking a Senior Director, Clinical Biomarkers to join an innovative biotech company. This is a permanent role with the opportunity to work remotely.Skills & Requirements:Education: PhD degree in Biology, Translational ...
Job Description : Senior Staff Regulatory Affairs Specialist is responsible for creating and executing regulatory strategies and objectives in alignment with business needs. This includes the preparation of regulatory submissions required to market new or modified medical devices in the U.S. an...
Zyston's client has requested our assistance in managing the hiring process for an IT Controls Assessment and Testing Specialist. This person will report to a manager whom Zyston placed in the role and work with a team of Zyston employees for our client. IT Controls Assessment and Testing Specialist...
Zyston's client has requested our assistance in managing the hiring process for an IT Controls Assessment and Testing Specialist. This person will report to a manager whom Zyston placed in the role and work with a team of Zyston employees for our client. IT Controls Assessment and Testing Specialist...
About Level2Level2 is a healthcare start-up that is building the next generation of virtual care for individuals with chronic conditions including Type 2 diabetes. This new business is dedicated to empowering patients to manage and achieve remission of their condition through an end-to-end virtual c...
About Level2Level2 is a healthcare start-up that is building the next generation of virtual care for individuals with chronic conditions including Type 2 diabetes. This new business is dedicated to empowering patients to manage and achieve remission of their condition through an end-to-end virtual c...
Description:Providence St. Joseph Health is calling a Senior Coding Quality Auditor (Full-Time, Days) to work remotely within our footprint states: AK, CA, MT, NV, OR, TX and/or WA.We are seeking a Senior Coding Quality Auditor to perform quality analysis of ICD and CPT codes as well as MS-DRG and A...
Job Title: Specialist Product Quality - REMOTE (JP9308) Location: Thousand Oaks, CA. (100% REMOTE) Employment Type: Contract Business Unit: PQ Synthetics and Quality Assurance Duration: 3 years Posting Date: 10/13/2021 3 Key Consulting is hiring a Specialist Product Quality for a co...
Senior Regulatory Affairs Specialist (Smith & Nephew, Inc., Memphis, TN):Prepare regulatory submissions such as: 510(k), technical files, design dossiers for new and modified devices. Work closely with project teams to develop regulatory strategies, testing requirements and other documentation to as...
Hillrom is a $2.8B leading worldwide manufacturer and provider of medical technologies and related services for the health care industry, including patient support systems, safe mobility and handling solutions, non-invasive therapeutic products for a variety of acute and chronic medical conditions, ...