Regulatory Writer Jobs in Arab, AL

Certified Workday Student Consultant / Workday Student Report Developer 100% Remote 12 Months If interested please share resumes to Workday Student Certification(s) Background in Workday Student Reporting of curriculum Academic Records Student Finance Financial Aid and crossfuncti More...

NC Department of Health and Human Services NC Medicaid Advance Planning Office is seeking an Advance Planning Writer with Medicaid NC FAST eligibility and/or Health and Human Services experience to join the Advance Planning Office. The primary role and responsibility of the Advance P More...

NC Department of Health and Human Services NC Medicaid Advance Planning Office is seeking an Advance Planning Writer with Medicaid NC FAST eligibility and/or Health and Human Services experience to join the Advance Planning Office. The primary role and responsibility of the Advance P More...

NC Department of Health and Human Services NC Medicaid Advance Planning Office is seeking an Advance Planning Writer with Medicaid NC FAST eligibility and/or Health and Human Services experience to join the Advance Planning Office. The primary role and responsibility of the Advance P More...

NC Department of Health and Human Services NC Medicaid Advance Planning Office is seeking an Advance Planning Writer with Medicaid NC FAST eligibility and/or Health and Human Services experience to join the Advance Planning Office. The primary role and responsibility of the Advance P More...

Job Title: Regulatory Project Management (RPM) Location: Foster City California preferred but open to remote candidates Job Duration: 9 months POSITION OVERVIEW: With increasing independence you will support other Development team members with project and/or process administrative More...

Drive our Machine Identity Security vision with a focus SSH keys and certificates. Responsiblefor defining product strategy developing our SSH Protect Product roadmap and prioritizing the product backlog and ensuring that the development team delivers features that provide maximum val More...

Description: Title: Environment Health and Safety Specialist II Shift: MoFr 7am 4pm (estimated start/end) Knowledge of building construction and demolition safety and environmental practices Knowledge of current national and state safety and environmental legislation Knowledge More...

Job Title: EHS Specialist (Remote) Client: Medical Device Manufacturing Company Location: Virtual Colorado 80239 Duration: 4 months Shift: 1st Shift Job Description Responsibilities may include the following and other duties may be assigned. Develops administers and implements enviro More...

Your CareerThe Supply Chain Compliance Manager will drive compliance  programs within the supply chain focusing on ensuring our products meet regulatory requirements.  This role includes staying current with global regulations conducting gap assessments and ensuring complian More...

Your CareerThe Supply Chain ESG Senior Program Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

As a Senior Information Developer (Technical Writer) at CyberArk youll be part of a motivated dedicated and experienced team that protects many of the largest organizations in the world.The primary focus of the User Assistance (UA) team is to help customers be successful when adopting More...

Description: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides administrative assistance in site selection study implementation and ongoing coordination of study sites either directly or via CROs. Moni More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...