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, ...
Regulatory Affairs Specialist/Senior - REMOTE - EUROPE Multiple Locations: United Kingdom • Poland • France • Belgium • Netherlands Requisition Number991Employment Type:Regular We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for ...
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...
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. ...
Requisition ID: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices 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 education in orthopedics. ...
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: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices 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 education in orthopedics. Arthrex...
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 ...
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 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...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC.This position will be 100% Remote.The Director/Sr. Director, Regulatory Affairs, CMC will also serve as a regulatory specialist on select project teams. Responsibilities:&nb...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Our client, a growing Pharma company focused in Oncology, is looking for a Director/Sr. Director, Regulatory Affairs, CMC. This position will be 100% Remote. This position is responsible for developing and implementing CMC regulatory strategies to facilitate the progress of R&D drug development a...
Job Title: Associate Director/Director, Regulatory Affairs CMC - RemoteThe Position: This organization is looking for a Regulatory CMC leader to apply experience and leadership to their Regulatory Affairs CMC team. You will be responsible for the overall management of a portfolio of biological produ...
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...
Description ABOUT US: As a not-for-profit organization, Mass General Brigham is committed to supporting patient care, research, teaching, and service to the community by leading innovation across our system. Founded by Brigham and Women’s Hospital and Massachusetts General Hospital, Mass ...
REMOTE TEMPORARY Coding Specialist Job Locations US-PA-West Reading Requisition ID 2021-36744 Hospital THMG Shift Day Department THMG Revenue Cycle Category Administrative/Clerical Hours per Pay Period 80 # of Openings 1 Position Type Temporary Full-Time Work Schedule Day shift- 8AM- 430pm or ...
Data Validation Specialist Our company specializes in enabling clinical trials research through advanced technologies and neurocognitive measurement. We combine innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. We are sea...
Data Validation Specialist Our company specializes in enabling clinical trials research through advanced technologies and neurocognitive measurement. We combine innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. We are sea...
Data Validation Specialist Our company specializes in enabling clinical trials research through advanced technologies and neurocognitive measurement. We combine innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. We are sea...
Data Validation Specialist Our company specializes in enabling clinical trials research through advanced technologies and neurocognitive measurement. We combine innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. We are sea...
Data Validation Specialist Our company specializes in enabling clinical trials research through advanced technologies and neurocognitive measurement. We combine innovative science and technology to advance and improve the clinical trials process for many leading pharmaceutical companies. We are sea...
EUROIMMUN US is an MDSAP registered, ISO 13485:2016, 21 CFR 820 compliant Medical device company that develops, manufactures, distributes, and performs service and installation activities of in vitro diagnostic test kits, instruments and software used in the detection of autoimmune status, allergies...
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...
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 ...
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...
Consistent and timely processing of coding rejection/denial appeals and customer concerns related to coding, including monitoring for patterns and trends, and ensuring appropriate reimbursement within regulatory requirements. Communicates trends, results and barriers to the leadership team. Identi...
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...
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up SpecialistRemote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this role you will be...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up SpecialistRemote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this role you will be...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up SpecialistRemote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this role you will be...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up SpecialistRemote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this role you will be...
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,...
Hamlyn Williams have partnered with an established global online gaming/sports betting company to bring on a Director of Government Affairs to manage all governmental affairs, public policy initiatives, and drive influence to align with the company's business interests. In this role you will:...
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...
Responsibilities: Identifies regulatory pathways for initial product designs and provides input to internal stakeholders Provides strategic input and technical guidance on global regulatory requirements to product development Assesses all requirements and potential obstacles for market acc...
Our client, a world leader in Life Sciences who is looking for Regulatory Affairs Specialist II(100% Remote).Job Title: Regulatory Affairs Specialist II (100% Remote)Job Type: Long-Term ContractLocation: Santa Clara, CA Responsibilities:• Manages regulatory responsibilities associated with the devel...