<p>We are seeking a skilled <strong>Corporate Attorney</strong> with specialized expertise in clinical trial operations and biopharmaceutical industries to join our dynamic team in Rockville, MD. The ideal candidate will possess significant legal experience advising on biopharma-related matters, including regulatory compliance, contract negotiation, intellectual property, and business transactions. This hybrid position allows a mix of remote work and in-office collaboration, requiring candidates to be local to the Rockville, MD area.Apply today! By sending an updated resume to Fana Belcher at [fana.belcher][at]roberthalf[dot][com].</p><p><br></p><ul><li><strong>Regulatory Compliance:</strong> Provide legal advice to ensure adherence to U.S. Food and Drug Administration (FDA), Intellectual Property, and other biopharma-relevant regulations.</li><li><strong>Contract Negotiation and Drafting:</strong> Prepare, review, and negotiate clinical trial agreements, licensing contracts, and collaboration agreements with CROs, biopharma companies, and other stakeholders.</li><li><strong>Risk Management:</strong> Identify risk areas related to clinical trials and ensure appropriate mitigation strategies.</li><li><strong>Corporate Operations:</strong> Advise senior management on operational legal matters, corporate governance, and business strategies.</li><li><strong>Intellectual Property:</strong> Provide legal expertise on patents, trademarks, and other forms of intellectual property relevant to the biopharma sector.</li><li><strong>Dispute Resolution:</strong> Represent the company in legal disputes, settlement negotiations, and arbitrations, particularly related to clinical trials and regulatory compliance.</li><li><strong>Collaboration:</strong> Work closely with cross-functional teams, including clinical research organizations (CROs) and business development, to support business goals while managing legal risks.</li></ul><p><br></p>

<ul><li>J.D. degree from an accredited law school and current bar membership in good standing.</li><li>Minimum of 5+ years of experience practicing law in corporate settings, preferably with exposure to clinical trials, biopharmaceuticals, and life sciences.</li><li>Hands-on experience with FDA regulations, clinical trial governance, and biopharma partnerships.</li><li>Exceptional negotiation, drafting, and analytical skills with attention to detail.</li><li>Strong understanding of intellectual property law and its applications in the biopharma industry.</li><li>Proven ability to balance legal risks with business objectives in a collaborative manner</li></ul><p><br></p>

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