[Remote] Associate Corporate Counsel, Compliance & Regulatory at Clairo

United States

Clairo Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Life Sciences, Clinical TechnologyIndustries

Requirements

Candidates must possess a J.D. from an ABA-accredited law school and be licensed in at least one U.S. jurisdiction. A minimum of 4+ years of legal and compliance experience, either in-house or at a law firm, is required. Experience in life sciences or clinical trials is strongly preferred, along with a proven ability to assess compliance risks and provide pragmatic counsel. The ideal candidate is a strategic thinker with sound judgment, business acumen, strong organizational and communication skills, high ethical standards, and discretion with sensitive information, comfortable working both independently and cross-functionally.

Responsibilities

The Associate Corporate Counsel, Compliance & Regulatory will lead enterprise-wide compliance initiatives across global operations, ensuring adherence to regulatory frameworks and fostering ethical business practices. This role involves advising on Sunshine Act reporting, anti-corruption, antitrust, and government contracting compliance, conducting risk assessments, and implementing mitigation strategies. Responsibilities also include developing and enhancing internal policies, investigating potential violations, overseeing the whistleblower program, delivering compliance training, monitoring regulatory developments, supporting the Audit & Risk Committee, assisting with M&A due diligence, responding to regulatory inquiries, supporting audits, and managing UBO/KYC and AML diligence requests.

Skills

Compliance
Regulatory Affairs
Risk Assessment
Policy Development
Internal Controls
Sunshine Act
Anti-corruption
Anti-bribery
FCPA
AML
KYC
Antitrust
Government Contracting
Whistleblower Reporting
Compliance Training
M&A Due Diligence
Legal Entity Maintenance
Governance
Clinical Technology
Life Sciences
Pragmatic Counsel
Strategic Thinking
Judgment

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees

Benefits

Competitive and equitable total rewards package
Physical, mental and financial health and wellness
Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.
The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.
AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.
The company has nearly 50 years of experience in clinical trial technology solutions.
Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.
The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.
Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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