Pictured: CSL manufacturing employee in Australia

Associate Director, Senior Counsel, Clinical

Entité: CSL Behring

Catégorie d’emploi: Legal

Famille d’emploi: Legal Business Partner

Type d’emploi: Full Time

Location: King of Prussia, Pennsylvania, United States

Référence de l'employeur: R-285025

CSL Behring

Description du poste

The Opportunity:

In collaboration with the Lead Counsel, Global Clinical Development, as the Associate Director, Senior Counsel, Clinical, you will provide practical, timely, and high-quality legal support to CSL’s Global Clinical Development function on a wide range of legal and regulatory issues. You will act as the primary escalation and resolution point for all clinical contracting legal queries for the Clinical Legal Department.

This is a hybrid role, requiring three (3) days of onsite work weekly. #LI-hybrid

The Role:

  • In support of the Clinical Development team, draft, review, and negotiate all agreements as directed by the Lead Counsel, Global Clinical Development, that are not otherwise managed by CRO, procurement, or clinical contracting teams.  This will include a range of bespoke agreements for which templates do not exist, for arrangements that are of key strategic importance for CDO and involve a high level of risk and complexity. Agreement types include but are not limited to clinical trial research agreements, clinical vendor agreements, clinical manufacturing agreements, and clinical trial supply.
  • Collaborate with the R&D/Strategy transactional legal team to support all clinical development components of the agreements supported by that team, ensuring CDO’s requirements are incorporated, and any issues appropriately escalated.
  • Provide advice with respect to a broad range of legal and regulatory issues related to CSL’s global clinical development activities.
  • Provide strong business partnering support for CSL’s Global Clinical organization, ensuring clear communication, strong collaboration and proper information flow.
  • Undertake any research on a range of clinical related legal and regulatory issues, as required by the Lead Counsel, Global Clinical Development, or the business.
  • Stay apprised of and generate training content on clinical legal issues and emerging external trends as required by the Lead Counsel, Global Clinical Development and Global Lead, Clinical Contracting for delivery to the business and to the clinical contracting teams.  Work in collaboration with the Clinical Contracts Operations Managers to efficiently deliver training content.
  • Act as the primary escalation and resolution point for any legal or contracting issues raised, and if necessary, escalate any unresolvable issues to the Lead Counsel, Global Clinical Development.
  • Draft, as assigned by Lead Counsel, Global Clinical Development, new templates required to support global clinical development. Review frequently negotiated agreement clauses, collaborate with the business to reassess the company’s risk appetite (as needed) and revise clauses accordingly.
  • As assigned, provide legal advice and support in connection with non-routine special projects for Global Clinical Development and for other matters or areas that business needs may dictate, or as otherwise required by the Lead Counsel, Global Clinical Development.  This will require strong cross functional, global collaboration.

Your Skills & Abilities:

  • Bachelor's Degree required.
  • Juris Doctor required.
  • Must be licensed to practice law in Pennsylvania or hold (or be eligible for and able to obtain promptly) a Limited In-House Corporate Counsel License under PA BLE Rule 302.
  • Minimum of 8 years practicing law, with 5 years of experience in a health care environment, preferably pharmaceutical or other organization engaged in clinical research. 
  • Strong familiarity with global clinical development laws and regulations (including GCP/ICH), and health care regulations (including fraud and abuse, anti-kickback, and FDA).
  • Experience in an international environment, in-house or private practice, highly desirable.
  • Ability to proactively identify, analyze, and effectively explain potential legal risks and complex legal issues to clients and develop creative and business-focused advice and solutions in order to facilitate the business objectives of the company while effectively managing risk.
  • Ability to maintain an independent and objective perspective while developing and maintaining a strong partnership with client groups.
  • Strong drafting and negotiation skills required, as well as ability to produce quality work under pressure and while balancing multiple priorities.
  • Strong communication, analytical, project management, problem solving, interpersonal, and teamwork skills are required.
  • Team player, self-motivated, able to demonstrate a history of successfully resolving challenging legal issues, and ability to effectively deliver sound and clear legal advice in a business setting.
  • Strong proficiency with Microsoft Office Suite (particularly with Word, Outlook, Teams, One Note, and Excel).

À propos de CSL Behring

CSL Behring est un chef de file mondial en biothérapeutique, mû par sa promesse de sauver des vies. Axée sur la satisfaction des besoins des patients grâce à l'utilisation des technologies les plus récentes, la société découvre, développe et fournit des thérapies innovantes aux personnes souffrant de troubles dans les domaines thérapeutiques de l'immunologie, de l'hématologie, des maladies cardiovasculaires et métaboliques, des maladies respiratoires et de la transplantation. Nous utilisons trois plateformes scientifiques stratégiques : le fractionnement du plasma, la technologie des protéines recombinantes et la thérapie cellulaire et génique, afin de soutenir l'innovation continue et d'affiner constamment les moyens par lesquels les produits peuvent répondre aux besoins médicaux non satisfaits et aider les patients à mener une vie pleine.

CSL Behring exploite l'un des plus grands réseaux de collecte de plasma au monde, CSL Plasma. Notre société mère, CSL, dont le siège social est à Melbourne, en Australie, emploie 32 000 personnes et offre ses thérapies vitales aux populations de plus de 100 pays.

Pour en savoir plus sur CSL, CSL Behring, CSL Seqirus et CSL Vifor, visitez https://www.csl.com/ et sur CSL Plasma, visitez https://www.cslplasma.com/.

Nos avantages sociaux

Pour plus d'informations sur les avantages sociaux de CSL, visitez Comment CSL soutient votre bien-être | CSL.

Votre place est chez CSL

Chez CSL, l'inclusion et l'appartenance sont au cœur de notre mission et de notre identité. Elles alimentent notre innovation au quotidien. En célébrant nos différences et en créant une culture de curiosité et d'empathie, nous sommes en mesure de mieux comprendre nos patients et nos donneurs et d'établir des liens avec eux, de favoriser des relations solides avec nos parties prenantes et de maintenir une main-d'œuvre diversifiée qui fera progresser notre entreprise et notre industrie vers l'avenir.

Pour en savoir plus sur l'inclusion et l'appartenance, visitez https://www.csl.com/careers/inclusion-and-belonging

Employeur offrant l’égalité des chances

CSL est un employeur offrant l'égalité des chances. Si vous êtes une personne handicapée et que vous avez besoin d'un aménagement raisonnable pour une partie du processus de candidature, veuillez visiter https://www.csl.com/accessibility-statement.

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