Lead Regulatory Affairs Associates and Coordinators in the regulatory management of clinical trial portfolio Independently prepare IRB documents, draft consent form and study documents, maintain regulatory files, and facilitate regulatory oversight of safety reporting. In concert with IND Sponsors, prepare and review IND submissions, communicate with the FDA, and prepare

WHO WE ARE We are the Metropolitan Council, the regional government for the seven county Twin Cities metropolitan area. We plan 30 years ahead for the future of the metropolitan area and provide regional transportation, wastewater, and housing services. We are committed to supporting a diverse workforce that reflects the communities we serve. Metropolitan Transportation S

Rutgers, The State University of New Jersey, is seeking a Grants Administrator for the Finance department at the Robert Wood Johnson Medical School. Under the direction of the Assistant Director of Finance, is responsible for the day to day support of all projects, grants, contracts and other restricted accounts and related functions associated with research, sponsored pr

Essential Duties & Job Functions Assists the Director of Financial Accounting with audit related requests for the Annual year end external audit, as well as DCAA/DCMA and other government agency audits, such as for Incurred Cost, CAS, Timekeeping, Post Award, and Provisional/Retroactive Billing Rates. Assists the Director of Financial Accounting in ensuring timely and acc

Collaborate closely with the Project Director and Eligibility Manager to align policy efforts with project goals. Provide essential technical assistance to state staff and eligibility reviewers, ensuring consistent policy application. Utilize your program knowledge to identify and address eligibility policy issues, promoting efficient and accurate processes. Assist in ide

Job description Our purpose Opening up a world of opportunity explains why we exist. Here at HSBC we use our unique expertise, capabilities, breadth and perspectives to open up new kinds of opportunity for our more than 40 million customers. We're bringing together the people, ideas and capital that nurture progress and growth, helping to create a better world for our cus

Coordinate internal and external resources to ensure the successful OTC certification. Implement weekly/monthly status meetings with the stakeholders and, when necessary, revise the schedule or budget to ensure that project requirements can be met Establish and maintain relationships with relevant client stakeholders, providing day to day contact on project status and cha

Counsel, Head of Global Regulatory Affairs Job Location(s) US CA Los Angeles Job ID 2024 1978 Category Legal/Compliance Department Legal Type Regular Full Time Position Summary Reporting to TCW's General Counsel, the Counsel, Head of Global Regulatory Affairs will lead TCW's regulatory affairs effort, including TCW's (i) engagement with domestic and global policymakers wi

This position will provide Regulatory Affairs oversight to Laerdal to assure FDA and Health Canada medical device and establishment requirements are met and both Laerdal Medical Corporation (LMC) and Laerdal Medical Canada (LMCA) remain compliant to medical device regulations. This position will provide Quality Assurance oversight to both the Laerdal Medical Canada (LMCA)

Provides global regulatory expertise to pre clinical, clinical, and commercial areas for investigational and marketed products. Ensures that regulatory/competitive intelligence, or scientific/regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Collaborates with Regulatory Management to establish clear regu

We are searching for a candidate to provide North America (including US and Canada) regulatory support for IFF Health and Biosciences business unit with focus on dietary supplement ingredients. The successful candidate will work as part of a global regulatory team within IFF Health and collaborate with internal business partners including R&D, Quality, Commercial and Mark

. Work Schedule and Additional Information Full time employment Work hours are 7 00 AM to 3 00 PM, Monday Friday, with 30 minute lunch. Telework You may have the opportunity to work from home (telework) part time, at the discretion of the supervisor. In order to telework, you must have a securely configured high speed internet connection and work from an approved location

OF WORK As part of this position, your responsibilities will include developing plans and estimates for a variety of work operations, such as construction, paving, and snow removal, under the supervision of subordinate managers. You will be responsible for recommending the allocation of resources, including equipment, manpower, and materials, to achieve program objectives

to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life changing treatments for patients with under addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis and uterine fibroids , as

The Data Governance Program Manager is responsible for supporting Data Governance across the organization, enabling business growth while ensuring compliance with risk and regulatory expectations. The position partners with various business and technology stakeholders to influence and drive adoption of related Enterprise Data Management strategies, policies, standards and