Legal Affairs Manager
$73.5k - $129.1kAmeriprise Financial Services, Inc.
About Our CompanyWe’re a diversified financial services leader with more than $1.5 trillion in assets under management, administration and advisement as of year-end 2024. Our team of 22,000 people across 19 countries, serves more than 3.5 million individual, small business and institutional clients. We are a longstanding leader in financial planning and advice, a global asset manager and an insurer. Our unwavering focus on our clients and strong financial foundation connects each of our unique businesses – Ameriprise Financial, Columbia Threadneedle Investments and RiverSource Insurance and Annuities. Here, we foster meaningful careers, invest in the future, and make a difference for clients, institutions and communities around the world.Job DescriptionAmeriprise Financial Services LLC has an exciting opportunity for a legal affairs manager position in the General Counsel's Office (GCO) Advice and Wealth Management Practice Group, supporting the company’s advisory products and services for retail customers. This position will support the Retail Investment Advice Legal team and will work on cutting edge, innovative products and services that represent the core value proposition of our business.Key Responsibilities:Issue spotting and application of the federal securities laws impacting all aspects of retail investment advice, including Regulation Best Interest, the Investment Advisers Act and applicable FINRA rules and state securities regulations.Conduct legal, factual and benchmarking research and prepare summaries of risk/legal analysis.Review marketing, training and other field facing materials.Draft various client facing disclosures and agreements to support new products/services and to address regulatory changes.Prepare and file updates to Forms ADV and BD.Maintain records, procedures and processes for maintaining agreements, disclosures and filings.Support the conflicts of interest program by monitoring and documenting conflicts of interest and associated controls.Cultivate and promote relationships with key business partners.Foster and promote a culture of compliance.Collaborate with Compliance personnel on relevant compliance related mattersRequired Qualifications:Associate’s degree or equivalent (2 years)3-5 years relevant experienceParalegal Certificate from ABA approved program or equivalent education/experienceSolid research and analytical skillsHighly organized and detail-orientedExhibits good working knowledge of products and services and business lines related to area of responsibilityDemonstrates increasing depth of knowledge of regulatory framework area of specialty and/or increasing breadth of knowledge in areas within and related to area of specialtyMake decisions quickly and appropriately using extensive expertiseAbility to learn and utilize new tools and technologiesPreferred Qualifications:JD or equivalent (6 years)Advanced subject matter expertise in business area being supportedPrevious experience negotiating agreementsFamiliarity with IARD filing systemIn-Office CollaborationWe are a client-centric, relationship-based business. Working together, in-person, is foundational to how we achieve results. By fostering a culture of face-to-face collaboration, idea sharing, productivity and personal connection, we deliver for our stakeholders — clients, advisors, employees and shareholders. Our employees work in the office at least four (4) days per week, with flexibility to work from home one (1) day per week. Some roles may require additional in-office time or different in-office expectations, and specific requirements will be discussed during the hiring process.Visa SponsorshipApplicants must have a valid work authorization that does not now, or in the future, require visa sponsorship for employment in the United States (e.g., H-1B, F-1 CPT, F-1 OPT, TN).Base Pay SalaryThe estimated base salary for this role is $73,500 - $129,100/year. We have a pay-for-performance compensation philosophy. Your initial total compensation may vary based on job-related knowledge, skills, experience, and geographical work location. In addition, most of our roles are eligible for variable pay in the form of bonus, commissions, and/or long-term incentives depending on the role. We also have a competitive and comprehensive benefits program that supports all aspects of your health and well-being, including but not limited to vacation time, sick time, 401(k), and health, dental and life insurances.Full-Time/Part-TimeFull timeExempt/Non-ExemptExemptJob Family GroupLegal AffairsLine of Business GCO General Counsel's OrganizationAmeriprise Financial is an equal opportunity employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ancestry, age, physical or mental disability, medical condition, pregnancy, military status, veteran status, genetic information, citizenship, disability status, marital status, family status or any other basis prohibited by law.We are committed to fostering an inclusive and accessible recruitment process for individuals with disabilities. If you require a reasonable accommodation to participate in the application or interview process, speak to your recruiter to discuss how we can support you.SummaryLocation: Minneapolis, Minnesota; Charlotte, North Carolina; New York, New York; Boston, MassachusettsType: Full time
$180k - $245k
...is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our... ...programs from early development through approval and lifecycle management.Ensure regulatory strategies align with corporate goals and evolving...Suggested$275k - $315k
...seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory strategy for our biologics... ...execution—from IND through BLA submission and approval. You will manage a small team of Regulatory Affairs professionals, providing...SuggestedFull timeTemporary workWork at officeLocal area3 days per week- Job-ID31521196Reference25-04484 The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval is maintained throughout the product lifecycle. GRA serves as the interface between the regulatory authorities and the program...Suggested
$190.4k - $285.6k
...technologies for authoring, review, data traceability, and knowledge management.Ensures programs are appropriately resourced and accountable... ...Bachelor’s Degree in Chemistry, Biology, Pharmacy, Regulatory Affairs, Pharmaceutical Sciences, Engineering, or related life...SuggestedFull timeSummer workRemote workFlexible hours2 days per week- ...86 Job Description: This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization... ...will contribute: With some supervision, plans, executes and manages regulatory submissions according to the regulatory strategy...Suggested
$177k - $278.08k
...patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization... ...regulatory compliance. Ensures project team colleagues, line management, and key stakeholders are apprised of developments that may...Minimum wageTemporary workLocal areaRemote workWorldwide- ...modified medical devices and other (regulated) products This role manages and submits 510ks for the products and manages communications... ...Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching...Work at office
- Job-ID31618053Reference25-04665 Responsibilities: The Regulatory Manager (RM) provides regulatory strategy and development guidance for... ...standards Serve as representative of Global Regulatory Affairs at project team meetings with both external and internal customers...Flexible hoursNight shift
$145k - $215k
...ll make an impact:Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs to serve as a key regulatory contributor and emerging strategic... ..., sexual orientation, citizenship, or any other legally protected class.CompensationKymera offers a competitive compensation...$120k - $140k
...communication to other departments.Participates in assigned Regulatory Affairs initiatives aimed at improving internal Idenix standards and... ...FDA submissions is required with the ability to successfully manage projects to deadlines. A working knowledge of electronic...Work at office$177k - $278.08k
...therapies to patients worldwide.The Director Global Regulatory Affairs, Neuroscience is responsible for developing innovative global... ...junior staff responsible. Ensures project team colleagues, line management, and key stakeholders are apprised of developments that may...Minimum wageTemporary workLocal areaRemote workWorldwide- ...A medical device company in Cambridge, MA, is seeking a Regulatory Affairs professional to lead regulatory strategies for Class II medical devices. Responsibilities include managing FDA submissions, ensuring regulatory compliance throughout product development, and collaborating...
$238k - $374k
...to patients worldwide.As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will... ...) to align evidence generation, usability/human factors, risk management, and value messaging to regulatory and access requirements for...Minimum wageTemporary workWork at officeLocal areaRemote workWorldwide$238k - $374k
...knowledge.Job DescriptionExecutive Director, Global Regulatory Affairs CMC Early DevelopmentAre you looking for a patient-focused... ...g., modeling/simulation, predictive tools, data and knowledge management, and digital CMC dossiers) to strengthen scientific justifications...Minimum wageTemporary workLocal areaRemote work$220k - $370k
...motivated and experienced Senior Director or VP of Regulatory Affairs. The ideal candidate will have a proven track record of leading... ...that shape product development, corporate strategy, risk management, commercialization, and successful product approvals Build...Full timeSummer workWork at officeFlexible hours$186.23k - $279.35k
...you passionate about science and experienced within regulatory affairs and drug development? Do you possess strategic and operational... ...to the development, commercialization and life cycle management of assigned products. Serves as the global regulatory lead (GRL...Hourly payFull timeTemporary workWorldwide3 days per week$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco... ...enable decisive, data-driven choices.Delivery and Milestone Management: Oversee all regulatory deliverables and milestones, including...Hourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week$242k - $313.5k
...life fully. Job Summary: The Senior Director, Regulatory Affairs CMC – Small Molecules provides senior-level scientific and... ...clinical development through NDA filing and post-approval lifecycle management, serving as the company's foremost authority on small molecule...Full timeLocal areaFlexible hours2 days per week$157k - $173k
...information, please visit avalynpharma.com and follow the company on LinkedIn . Position Summary: The Senior Manager, Regulatory Affairs will support the development and execution of the global regulatory strategy and execution for Avalyn’s development-stage...Full timeLocal area$245k - $300k
...Description Job Description Description: Sr. Director, Regulatory Affairs At Merida Biosciences, we are pioneering true precision... ...expert, partnering closely with Program Leadership & Management, Clinical Development, Clinical Pharmacology, Clinical Operations...Local area- ...We are proud to partner with an innovative biotechnology company in the search for a Senior Director, Regulatory Affairs . This fully remote role (US or Canada) will lead regulatory strategy, execution, and compliance across discovery, development, and manufacturing, with...Remote work
- ...Beeline Medicines in the United States is seeking a Senior Director, Regulatory Affairs CMC – Small Molecules to lead regulatory strategy for all CMC activities across the immunology and inflammation portfolio. You will shape global regulatory submissions, oversee IND/...
$225k - $250k
...seeking an experienced Director of Regulatory Affairs – Advertising & Promotion to serve as a... ...authority for assigned products, managing reviewers within their therapeutic area.... ...submissions as needed. Partner with Marketing, Legal, Medical Affairs, and other business...Full timeWork at officeFlexible hours3 days per week- Arbor Biotechnologies, based in Cambridge, MA, is seeking a Manager, Regulatory Affairs, to support regulatory execution across internal and partnered programs, health authority interactions, and cross-functional activities toward IND/CTA submissions. You will lead regulatory...
- The Director of Regulatory Affairs provides strategic and operational leadership to the development and commercialization of products... ...facilitate assessment of IND and NDA applications. Organize and manage meetings with Health Authority personnel to obtain commitments...
- Partner closely with the Director of Regulatory Affairs to define and implement regulatory strategies for new product development, product modifications, and lifecycle management of Class II medical devices. Provide regulatory guidance during product development to ensure...
- Senior Manager - Regulatory Affairs Operations Location - Cambridge, MA (Hybrid) Oncology Biotech | Global Clinical Programs I’m currently supporting an innovative clinical-stage biotechnology company developing next-generation therapies in oncology. With multiple clinical...
$238k - $294k
...Position Description The Sr. Director, Regulatory Affairs Advertising, Promotion and Labeling (LAP)... ...Development, Medical Affairs, Commercial, Legal, and Safety, and plays a central role in labeling strategy, lifecycle management, and promotional material review in a...Full timeWork at officeFlexible hours3 days per week$115k - $135k
...recognition. That’s who thrives at Arbor. If this resonates, read on. About the Role Arbor Biotechnologies is seeking a Manager, Regulatory Affairs, to support an expanding portfolio of gene editing programs. Reporting to the Director of Regulatory Affairs, this...- Senior Regulatory Affairs Manager- REMOTE I'm looking for a senior manager, regulatory affairs to lead our growing, dynamic team through global phase 3 clinical trials of a certain product and support other clinical studies. This role includes driving global submission...Full timeRemote work
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