Source Job

• Advise on regulatory compliance matters across jurisdictions.
• Support business units on pharmacy operations and supply chain issues.
• Assist with responses to regulatory inquiries and complaints.

Hims & Hers is a health and wellness platform that aims to improve people's health through accessible care. They are a public company traded on the NYSE with a talent-first flexible/remote work approach.

• Co-ordinate and compile regulatory submissions and agency correspondence for assigned projects
• Implement action plans to achieve timely approval of submissions ensuring compliance
• Participate in and support project teams to achieve regulatory goals

Jobgether is acting as a job platform partnering with other companies. They utilize an AI-powered matching process to ensure fair application reviews, identifying top candidates for client companies, though final hiring decisions are managed by the client's internal team.

• Be the RA representative on core functional teams for advertising and promotion and global software regulatory classification.
• Work closely with SW development, engineering, architect, quality and cybersecurity teams.
• Represent RA in the assessment of global cybersecurity and data privacy initiatives.

Dexcom Corporation is a pioneer and global leader in continuous glucose monitoring (CGM). They have broadened their vision beyond diabetes to empower people to take control of their health with personalized, actionable insights. Dexcom has thousands of ambitious, passionate people worldwide.

• Coordinate and compile regulatory submissions.
• Implement action plans for approval of submissions.
• Improve internal processes and foster relationships.

They are a company using AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. They identify the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

• Build and mature core elements of Rula’s enterprise Compliance Program.
• Ensure adherence to federal and state healthcare regulatory requirements across Rula’s clinical operations.
• Lead compliance risk assessments and internal controls; oversee investigations and corrective action processes.

Rula is dedicated to treating the whole person and aims to create a world where mental health is no longer stigmatized. Rula is a remote-first company that is passionate about making a positive impact on the lives of those struggling with mental health issues.

• Provides regulatory guidance throughout the clinical development life cycle.
• Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees to assure compliance with regulatory standards.
• Keeps abreast and continually expands knowledge of laws, regulations and guidelines governing drug development and approval.

Precision Medicine Group is a company that works in the clinical trial space. They are an equal opportunity employer that values diversity and does not discriminate based on race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

• Own the monitoring, analysis, and interpretation of state and federal legislation, regulations, and administrative rules.
• Review, redline, and propose changes to legislation and regulations and evaluate proposals for impact, compliance, and risk.
• Engage directly in the legislative process alongside the Government Affairs & Public Policy team.

Proof is shaping the legal and regulatory environment surrounding digital identity, remote online notarization, future of workforce, privacy, AI governance, and fraud prevention technologies. They aim to ensure its platform remains compliant, secure, and trusted.

• Anticipate and help shape hemp beverage regulations.
• Serve as the primary internal expert on state hemp beverage regulations.
• Lead and develop the compliance function as Willie's Remedy+ scales nationally.

JuneShine Brands is building an innovative social tonic platform. They comprise distinct brands, each with its own ethos and purpose, and is composed of a diverse and dynamic group of individuals and committed to fostering an inclusive environment.

• Provides regulatory guidance throughout the clinical development life cycle.
• Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees to assure compliance with regulatory standards.
• Serve as representative of Global Regulatory Affairs at project team meetings with both external and internal customers

Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and data sciences, focusing on Oncology and Rare Disease. The company values employee contributions and nurtures ideas, striving for positive change.