Senior Clinical Outsourcing Contracts Manager

🔥 17 horas atrás

🏄 California – Remoto

🏄 California – Remote

💵 $148.500 - $203.000 / ano

⏰ Tempo Integral

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👔 Gerente

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Neurocrine Biosciences

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

🧬 Biotecnologia

🏥 Saúde

💊 Farmacêutico

Biotechnology • Healthcare • Pharmaceuticals

A Neurocrine Biosciences é uma empresa biofarmacêutica líder focada em neurociência, com um propósito simples: aliviar o sofrimento de pessoas com grandes necessidades, mas poucas opções. Somos dedicados a descobrir e desenvolver tratamentos que mudam a vida de pacientes com distúrbios neurológicos, neuroendócrinos e neuropsiquiátricos pouco atendidos. O portfólio diversificado da empresa inclui tratamentos aprovados pelo FDA para discinesia tardia, coreia associada à doença de Huntington, endometriose* e fibromas uterinos*, além de um pipeline robusto incluindo vários compostos em desenvolvimento clínico de fase intermediária a avançada em nossas principais áreas terapêuticas. Por três décadas, aplicamos nosso conhecimento único em neurociência e nas interconexões entre sistemas cerebrais e corporais para tratar condições complexas. Buscamos incansavelmente medicamentos para aliviar o peso de doenças e distúrbios debilitantes, porque você merece uma ciência corajosa.

Descrição

• Manage outsourcing and contracting activities supporting clinical research, primarily clinical trials • Partner with Clinical Research Organizations and other vendors to ensure efficient, compliant, and high-quality clinical program execution • Lead negotiation and administration of clinical research agreements • Work cross-functionally with Clinical Operations, Legal, Finance, and study teams • Lead RFI and RFP processes across all phases of clinical trials and related services • Support vendor selection, coordinate RFPs and bid defenses, and negotiate work orders and change orders • Lead outsourcing strategies, including supplier selection and ongoing supplier management • Negotiate, administer, and execute complex agreements with global service providers, vendors, research collaborators, and clinical trial sites • Ensure contracts comply with regulatory requirements, ethical standards, company policies, and procedures • Manage the full contract lifecycle from request intake through execution in alignment with study timelines • Review, draft, redline, and negotiate clinical agreements and templates • Identify contractual risks, escalate issues, and drive resolution • Negotiate favorable terms and budgets focused on cost control, risk mitigation, and preventing scope creep • Partner with Finance and Accounting on contract budgets and payment terms • Ensure accuracy, consistency, and compliance across contract documentation • Monitor contract turnaround times and drive process improvements • Contribute to improving contracting, budgeting, and payment processes • Perform other duties as assigned

🎯 Requisitos

• BS/BA degree in business administration or health care/science related field AND 8+ years of experience in a CRO, Biotech or Pharmaceutical organization; OR Master's degree in business administration or health care/science related field AND 6+ years of similar experience • Experience with contract management, negotiation, budgeting and administration including billing/invoicing, issue resolution, and serving as point of contact for CRO • Ability to recommend relevant process, technical, or service improvements • Broad expertise or unique knowledge; considered an expert within the company • In-depth expertise in the discipline and broad knowledge of related areas • Ability to work as part of and lead multiple teams • Good leadership and mentoring skills • Excellent computer skills • Excellent communication, problem-solving, and analytical thinking skills • Ability to meet multiple deadlines across varied projects/programs with accuracy and efficiency • Excellent project management and strong project leadership skills • Expertise managing complexity and multiple work streams in changing circumstances • Advanced knowledge of clinical trial processes, regulations, and guidelines • Proven success working effectively across a matrix organization • Ability to prepare and negotiate external provider master service agreements, work orders, and change orders, and track them for clinical operations • Ability to read and interpret complex clinical contracts and ensure terms meet company standards • Expert contract administration skills, including budgets, billing/invoicing, issue resolution, and serving as CRO point of contact • Advanced knowledge of clinical contract accounting and budgeting processes • Advanced understanding of drug development and clinical operations

🏖️ Benefícios

• Annual bonus with a target of 30% of the earned base salary • Eligibility to participate in equity based long term incentive program • Retirement savings plan with company match • Paid vacation • Paid holiday and personal days • Paid caregiver/parental and medical leave • Medical, prescription drug, dental and vision coverage