A company is looking for a Senior Regulatory Affairs Specialist, Medical Devices. ...
Regulatory Affairs Specialist (R&D/QA)Fort Worth, TX 76104 (*Local candidates- 3 days on site/2 days remote)$43-$45hr (Weekly pay + Benefits)1yr contract (Excellent potential for extension or permanent)Full-time- M-F 8am-5pmOur client is a global team of innovators, leaders, creators, builders, and ...
A company is looking for a Senior Regulatory Affairs CMC Associate. ...
Position: Regulatory Affairs Specialist I, Req#: 3335-1. Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. Prepare responses to customer requests for infor...
A company is looking for a Senior Counsel, Product and Regulatory Affairs (Liquidity). ...
Regulatory Affairs Associate Director/Director. Regulatory Affairs (strong preference for experience in oncology). This role provides leadership in the strategic guidance and execution of regulatory concepts within cross-functional project teams and. Present Regulatory strategies and issues. ...
GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy. Work with global regulatory affiliates to compile global regulatory impact for changes on commercialized medical device products. Perform regulatory assessments for US, EU, and Canada for changes on commerciali...
The Regulatory Affairs Coordinator I is new to research regulatory affairs with limited or no regulatory affairs knowledge. This person is responsible for assisting other regulatory affairs employees with specific tasks including filing, binder preparation and maintenance, basic IRB submissions and ...
Regulatory Affairs Specialist (R&D/QA). Regulatory affairs, and/or experience in Quality Assurance, (R&D), Manufacturing preferably within IVDR (Vitro Diagnostic Regulation). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Resea...
Regulatory Affairs Coordinator II. Regulatory Affairs Coordinator II. Conducts study start-up activities and prepares/maintains all regulatory documents. Prepares documents and facility for external audits by the sponsor or various regulatory agencies. ...
The Regulatory Affairs Coordinator I is new to research regulatory affairs with limited or no regulatory affairs knowledge. This person is responsible for assisting other regulatory affairs employees with specific tasks including filing, binder preparation and maintenance, basic IRB submissions and ...
Regulatory Affairs professionals; provide invaluable strategic, technical, and regulatory advice to help clients with their various innovative product applications; and manage client relationships. Provide expertise in interactions with regulatory agencies (such as FDA) and provides expertise on reg...
Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. Prepare responses to customer requests for information, such as product data, written regulatory affairs ...
The Director, Regulatory Affairs will represent Invenergy before and manage relationships with state economic and environmental regulators, transmission system operators, and regional trade associations in Texas on behalf of Invenergy's existing assets as well as its pipeline of development projects...
Operate as the primary point of contact for Quality and Regulatory Affairs representation for DH product development and maintenance of marketed products and will oversee the end-to-end Regulatory Affairs and Quality strategies for DH products. DIRECTOR, QUALITY AND REGULATORY AFFAIRS, DIGITAL HEALT...
Regulatory Coordinator II - Hybrid Opportunity. Looking to hire an individual with strong regulatory and clinical research experience to act as a . Conducts study start-up activities and prepares/maintains all regulatory documents. Prepares documents and facility for external audits by the sponsor o...
We’re currently seeking a highly experienced Clinical Regulatory Leader, Health Authority Medical Review Team Lead, Master/Senior Medical Review Officer who is looking to draw upon their wealth of experience in clinical trial design and drug development to join Parexel’s highly recognized Regulatory...
In this highly visible role, you will partner with a large, global pharmaceutical company and provide CMC regulatory strategy input and expertise in the area of investigational, new and marketed biologic and small molecule drug products to assigned project teams, to ensure client's products are deve...
The Collateral Compliance Specialist is responsible for ensuring adherence to internal policies and procedures, laws, and industry/banking regulations. ...
A company is looking for a Lead Information Security Analyst, Compliance (Remote Work Option). ...
A company is looking for an Associate Regulatory Product Counsel to support its Banking-as-a-Service initiatives. Key Responsibilities:Provide legal and regulatory guidance on federal and state consumer lending and payments lawsStay updated on relevant banking and lending regulations and trendsPerfo...
A company is looking for an Associate, Regulatory Affairs to join their Compliance team. ...
A company is looking for a Principal Program Manager to develop and implement compliance strategies in the security domain. ...
A company is looking for a Director of Regulatory Affairs, Lifecycle. ...
A company is looking for a Pharmacist - Prior Authorization to perform clinical reviews and support pharmacy initiatives remotely. ...