As part of the Web Operations team, responsible for providing support to 14 divisions, the Digital Production Specialist supports the maintenance and development of digital properties , as well as special projects where needed . The Digital Production Specialist balances web design and technical apt...
The Proposal Design Specialist is responsible for desktop publishing and The Proposal Design Specialist is responsible for desktop publishing and formatting documentation in support of proposals . The Proposal Design Specialist partners with proposal managers, coordinators, technical subject matter...
As a Manager, you will be responsible for processes and/or serve as a primary contact for key external relationships within a department. Provide guidance and/or establish framework and create and execute project plans. This will be an induvial contributor role and report to an Associate Director, ...
Job ID RDate posted Aug. 19, 2021Location RemoteBy clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda'sPrivacy Notice and Terms of Use . I further attest...
*Summarized Purpose:*Manages a large, regional and/or global team of staff and managers within the department and provides innovative solutions including regulatory expertise and client interface to provide strategic regulatory intelligence and guidance for product development from preclinical throu...
Title: Regulatory Publisher Location : Remote Full time ECTD Publishing 2 - 3 years of experience in eCTD Publishing Should have experience in Document Level publishing (DLP) and Submission Level Publishing Should know Lifecycle Management Submissions, such as Safety, Promotional & other...
Title: Regulatory Publisher Location : Remote Full time ECTD Publishing 2 - 3 years of experience in eCTD Publishing Should have experience in Document Level publishing (DLP) and Submission Level Publishing Should know Lifecycle Management Submissions, such as Safety, Promotional & other ...
Job Description For this specific project they will be performing site consolidation, they are taking 61 practice sites (for ex. Sterling primary care practices) and they will be consolidating them into 2 sites. They will be responsible for performing and updating accurate web content in a ...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring me...
Specialty Pharmaceutical Company has remote contract role for 6 months (to start; often go longer)CORE ACCOUNTABILITIES:Manage and performs daily operational activities for regulatory submissions (project management, resource scheduling, formatting, publishing, QC, archive and submission); may suppo...
Specialty Pharmaceutical Company has remote contract role for 6 months (to start; often go longer)CORE ACCOUNTABILITIES:Manage and performs daily operational activities for regulatory submissions (project management, resource scheduling, formatting, publishing, QC, archive and submission); may suppo...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring me...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring me...
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...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toge...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toge...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toge...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toge...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toget...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toget...
HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve toget...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
*The Role*Do you want to lead a high energy team focused on transforming the way Life Sciences companies bring drugs to market? Do you have a relentless passion for delivering successful software implementations? We are looking for curious individuals who enjoy navigating the unknown, who can innova...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
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 vi...
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, ...
Technical SEO Specialist (Remote/Hybrid)Remote/London £50kMy client, an award-winning Publishing House, is looking for a talented Technical SEO Specialist to work on a wide range of projects across the group. This role is key to continuing the growth in natural search traffic for AgencyThis position...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
Description: This position has the option to telecommute on a full time basis if within a commutable distance to one of the posted locations. Job Purpose This role will be responsible for driving activities associated with the Request for Proposal (RFPs) process. By joining our team, you w...
Career CategoryResearchJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you're part of something bigger, it's because you are. At Amgen our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are globa...
Job DetailsLevelExperiencedJob LocationPrinceton, NJ - Princeton, NJRemote TypeFully RemotePosition TypeFull TimeSalary Range$51,500.00 Salary/yearJob CategoryStrategy - PlanningProduction Specialist, Print on Demand (Remote Option)Princeton University Press (PUP) seeks a skilled individual who is p...
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 ...
Equity Staffing is looking for a Talent Acquisition Specialist, Telecommute. This position with a Fortune 100 organization. Our client serves more than 85 million people and has a reputation for bold ideas. If you enjoy working with energetic people in a collaborative environment, we want to speak w...
Job Overview: Labcorp Drug Development is seeking candidates for a Manager, Regulatory Submissions. The Manager, Regulatory Submissions will be remotely (home-based) located anywhere within the United States or Canada. The Manager, Regulatory Submissions will be responsible for ensuring the timely s...
Do you have a heart for equipping the local church? Do you enjoy using your technical design skills to engage diverse audiences? Are you skilled in collaborating with other designers and content creators to develop exceptional digital and print assets? Apply today to explore if this is where God is ...
Overview:Do you have a heart for equipping the local church? Do you enjoy using your technical design skills to engage diverse audiences? Are you skilled in collaborating with other designers and content creators to develop exceptional digital and print assets?Apply today to explore if this is where...
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. ...
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...
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...