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Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus...
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$138.5k - $186k
...application is true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements: Bachelor’s degree in a scientific...
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Full time
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Worldwide
...Manage Lupin's existing REMS programs and help in the development of new REMS programs (as needed) with the support of the supervisor... ...REMS and other patient safety programs. Works closely with Phar Regulatory Affairs, Manager, Regulatory, Operations, Product Development,...
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...Responsibilities:
ROLE AND RESPONSIBILITIES:
Manage Lupins existing REMS programs and help in the development of new... ...operations
Responsible for maintaining and updating various regulatory databases to ensure accuracy of information
Any additional responsibilities...
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...therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Regulatory Data Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence function, responsible for driving data...
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...Summary
To coordinate and author complex documents needed for regulatory submissions, ensuring the coordination and integration of the... ...document subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.
Participate...
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Worldwide
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...help along the way.
ROLE AND RESPONSIBILITIES:
~ Manage Lupin’s existing REMS programs and help in the development of new... ...~ Responsible for maintaining and updating various regulatory databases to ensure accuracy of information
~ Any additional...
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..., please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
Senior Manager, Global Regulatory Strategy, US & Canada, AbbVie Inc., Madison / Florham Park (Morris County) New Jersey
Responsible for the development...
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Holiday work
Temporary work
...healthcare and serve as a leader of positive change.
The Regulatory Specialist is responsible for promoting compliance with Federal... ...terminology.
Ability to work in a fast-paced environment and manage competing tasks and demands.
Licenses and Certifications...
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Local area
...393223BR
Senior Regulatory Writer
USA... ...This is a Remote Position
1.To author, review and manage high quality clinical and safety documents: complex Clinical Study...
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Full time
Remote job
Relocation bonus
Shift work
...OVERVIEW
For the LVMH Beauty scope of brands, joining the Regulatory Affairs & External Relations team to lead the operational regulatory... ...Affairs experience
~5 years of demonstrated people-management experience
~ Strong computer skills (PowerPoint and MS Excel...
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Full time
Flexible hours
...at Bank of America in Newark, Delaware, United States
Regulatory Business Control Manager
Charlotte, North Carolina;Belfast, Maine; Plano, Texas; Richmond, Virginia; Phoenix, Arizona; Chandler, Arizona; Tampa, Florida; Chicago, Illinois; Newark, Delaware; Jacksonville...
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Work experience placement
Relief
Shift work
Day shift
...rare conditions.
Could you be our next Director of Regional Regulatory Vaccines Lead? The job is located in the Summit NJ or King of Prussia... ...Global Regulatory Affairs Strategy Team (GRAST) members to manage and resolve issues.
Ensure strategic regional regulatory...
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Summer work
Worldwide
...partnering with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development plans... ...products); provide regulatory support and guidance and manage day-to-day regulatory activities. Collaborate with all disciplines...
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...Director takes an active role in facilitating and coordinating regulatory activity for the enterprise and its facilities. The Director... ...verbal communication skills;
* Strong analytical and project management skills
* Demonstrated capability to interact directly with C...
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Temporary work
Work experience placement
Local area
Flexible hours
...possibility of extension
•Hybrid schedule (require to be onsite for 3 days/week -Tuesday and Wednesday fixed) 3rd day is optional.
•Manager will prefer someone with experience over a degree/education.
Responsibilities:
•Under general supervision, responsible...
3 days per week
...disorders.
Summary
Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic... ...side, as needed. Provide RA specific inputs into CDx Risk Management plans for individual projects/indications. Assist the CDx team...
Local area
The Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives. This role involves actively contributing to the development and execution of regulatory...
Local area
Overview:
The Senior Director, Regulatory Affairs- GDP provides strategic oversight and direction for regulatory activities on a regional... ...fostering collaboration with regional regulatory authorities, managing regulatory risks and opportunities, and providing strategic...
Local area
...Join Our Growing Team!
We are looking for a Senior Director - Regulatory Affairs to join our US team. This role is responsible for... ...comprehensiveness, or compliance with regulatory standards.
Manage activities such as assistance or coordination of audits, regulatory...
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