Regulatory Licensing Manager

Block Oakland , CA 94604

Posted 2 months ago

Block is one company built from many blocks, all united by the same purpose of economic empowerment. The blocks that form our foundational teams - People, Finance, Counsel, Hardware, Information Security, Platform Infrastructure Engineering, and more - provide support and guidance at the corporate level. They work across business groups and around the globe, spanning time zones and disciplines to develop inclusive People policies, forecast finances, give legal counsel, safeguard systems, nurture new initiatives, and more. Every challenge creates possibilities, and we need different perspectives to see them all. Bring yours to Block.

Block relies on licenses from state and federal financial regulators throughout the U.S to issue many of its products. The core mission of the Regulatory Licensing Manager is to uphold Block's licensing and other regulatory obligations in the lending space. You will track regular license maintenance requirements, timely filing regulatory reports and regulatory submissions and communicate with regulators. You will partner with members in legal, finance, analytics, product and other teams, to ensure that Block is compliant with applicable requirements while streamlining regulatory impact and facilitating innovation. You will report to the Counsel Regulatory Lead.

You will:

  • Co-manage a licensing program that fulfills our legal and regulatory responsibilities, while endeavoring to minimize business and product impact

  • Complete regulatory reporting requirements by gathering data from multiple and disparate internal stakeholders, harmonizing data and ensuring that all reports are submitted with care and on time

  • Manage all assigned licensing requirements and partner with all partners as necessary

  • Manage employee specific licensing registrations on state by state basis for lending operations personnel

  • Manage third party licensing vendors and coordinate work orders

  • Daily license maintenance and management of regulatory records

  • Support examination preparation and submissions

  • Maintain relationships with all partners and state and federal regulators and respond to regulatory requests in a timely manner

  • Manage assigned work with a team-oriented approach

You have:

  • 3+ years experience in legal, compliance, or regulatory affairs, preferably in the lending space

  • Experience with licensing maintenance and management, preferably in lending; NMLS and examination experience a plus

  • Familiarity with lending regulations and financial services industry best practices

  • Have a high attention to detail working in a strict deadline-driven environment

  • Passion for creating and implementing efficient operational and logistical efficiencies

  • Experience interpreting and articulating legal and regulatory obligations to regulators and team members

We're working to build a more inclusive economy where our customers have equal access to opportunity, and we strive to live by these same values in building our workplace. Block is a proud equal opportunity employer. We work hard to evaluate all employees and job applicants consistently, without regard to race, color, religion, gender, national origin, age, disability, veteran status, pregnancy, gender expression or identity, sexual orientation, citizenship, or any other legally protected class.

We believe in being fair, and are committed to an inclusive interview experience, including providing reasonable accommodations to disabled applicants throughout the recruitment process. We encourage applicants to share any needed accommodations with their recruiter, who will treat these requests as confidentially as possible. Want to learn more about what we're doing to build a workplace that is fair and square? Check out our I+D page.

Additionally, we consider qualified applicants with criminal histories for employment on our team, assessing candidates in a manner consistent with the requirements of the San Francisco Fair Chance Ordinance.

Perks

We want you to be well and thrive. Our global benefits package includes:

  • Healthcare coverage

  • Retirement Plans

  • Employee Stock Purchase Program

  • Wellness perks

  • Paid parental leave

  • Paid time off

  • Learning and Development resources

Block, Inc. (NYSE: SQ) is a global technology company with a focus on financial services. Made up of Square, Cash App, Spiral, TIDAL, and TBD, we build tools to help more people access the economy. Square helps sellers run and grow their businesses with its integrated ecosystem of commerce solutions, business software, and banking services. With Cash App, anyone can easily send, spend, or invest their money in stocks or Bitcoin. Spiral (formerly Square Crypto) builds and funds free, open-source Bitcoin projects. Artists use TIDAL to help them succeed as entrepreneurs and connect more deeply with fans. TBD is building an open developer platform to make it easier to access Bitcoin and other blockchain technologies without having to go through an institution.

icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Associate Director Regulatory Medical Writing

Organon & Co

Posted 1 week ago

VIEW JOBS 6/22/2022 12:00:00 AM 2022-09-20T00:00 Job Description Organon is a Women's Health Company that believes in a better and healthier every day for every woman! We are a passionate, global community of thousands dedicated to redefining the future of women's health. Our mission is to deliver impactful medicines and solutions for a healthier every day. But what really makes it work at Organon is our people. We're looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress. At Organon, you'll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a Fortune 500 company with an international footprint that serves people in more than 140 markets. It's going to be an exciting future-come be a part of it! THIS ROLE CAN BE 100% REMOTELY BASED. This role is accountable for Regulatory Medical Writing (RMW) and is part of the Regulatory Operations organization. The successful candidate should expect to provide medical writing of clinical and safety regulatory documents supporting components across various types of regulatory filings, including but not limited to: Protocol Amendments for inline trials, aggregate safety reports (DSUR, PSUR/PBRER, PADER, Annual Reports), Agency Background Packages and Response to Agency Inquiry, 2.5 Clinical Overviews, Clinical and Non-Clinical expert statements, and RMPs. Other responsibilities would also include maintenance of common templates and provide content management support (i.e., formatting, citations, content authoring tool workflow facilitation). This position will be required to coordinate routinely with leadership in the Product Registration (Regulatory Liaison) organization, Medical/Clinical/Safety organizations (with CRO), and IT. This position will be a member of the Regulatory Medical Writing Team, reporting into Director, Medical Writer. Primary Responsibilities: * Interact with therapeutic/functional area leaders to execute on organizational priorities. * Ensures timely and high-quality completion of Medical Writing deliverables that include the proper content and context and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards. * Drive interaction and clear handoffs between stakeholder SME organizations (Clinical, Safety, Regulatory, Non-Clinical) to the RMW team. * Support and drive partnering with vendors to provide Medical Writing support. * Lead the development, alignment, and consistent implementation of processes. * Ensures appropriate systems in place such that quality assurance review of documents occurs. * Drive the preparation/revision of document templates, development of process, and preparation/revision of standard operating procedures (SOPs) and guidance documents. * Develops and drives process supporting content authoring and formatting to a standard within the global content authoring platform. * Participates in Clinical Research Organization (CRO) alliance and other outsourcing activities. * Provides strategic direction and oversight of multiple contractor (partner) RMW's composed of senior/experienced RMW and junior RMW roles. Education Minimum Requirements: * Bachelor of Science Degree in Life Sciences or Health Care Professions (Nursing/ Pharmacy) or related discipline. * Master's degree / PhD / PharmD preferred. Required Experience and Skills: * At least 8 years of relevant pharmaceutic experience is required; with majority of this in medical writing role. * Experience as lead writer for key documents included in major US/EU and/or international regulatory submissions required. * Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products. * Understanding of FDA/international regulations, ICH guidelines, and applicable US/international regulatory processes related to document preparation and production (including CTDs). * Must have proven track record to be able to think critically, strategically, independently and problem solve. * Must have high level of motivation, drive, and demonstration of our new company's leadership values. * Excellent time and project management skills. * Excellent written and verbal communication skills including ability to write clearly and concisely. * Top notch interpersonal skills in difficult situations. * Ability to collaborate across multiple functional areas. Who We Are: Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman. Subject to applicable law, all prospective US Organon hires will be required to demonstrate that they have been fully vaccinated against COVID-19 with a vaccine authorized or approved by the Food and Drug Administration (FDA), or qualify for a medical or religious accommodation to this vaccination requirement, as a precondition of employment. Residents of Colorado: to request this role's pay range: email: coloradopayact@organon.com Jersey City and New York City Positions: to request this role's pay range and benefits, email: jcnycpayact@organon.com US and PR Residents Only If you require reasonable accommodation(s) in completing an application, interviewing, or otherwise participating in the employee selection process, please email us at staffingaadar@organon.com. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement OFCCP Pay Transparency Rule Organon is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully Organon LLC., does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Remote Work Shift: Valid Driving License: Hazardous Material(s): Number of Openings: 1 Requisition ID:R509662 Organon & Co Oakland CA

Regulatory Licensing Manager

Block