Site Contract Manager, II

🕒 Agosto 11

🌲 North Carolina – Remoto

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💵 $47.000 - $95.900 / ano

⏰ Tempo Integral

🟢 Júnior

🟡 Pleno

👔 Gerente

🦅 Patrocina Visto H1B

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👻 Score fantasma 2%

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🗣️🇺🇸🇬🇧 Inglês obrigatório

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Syneos Health

10.000+ funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

Healthcare • Consulting • Logistics

Syneos Health é uma organização líder, totalmente integrada, de soluções biofarmacêuticas, criada para acelerar o sucesso dos clientes. A empresa transforma insights exclusivos clínicos, de Assuntos Médicos (Medical Affairs) e comerciais em resultados para responder às realidades modernas do mercado. Ao utilizar tecnologias avançadas e insights, a Syneos Health colabora com os clientes para acelerar a entrega de terapias importantes a pacientes no mundo todo, oferecendo serviços que abrangem todo o espectro do clínico ao comercial.

Descrição

• Negotiate clinical trial budgets from start to finish directly with clinical sites from a Sponsor perspective • Understand budget and contract language for Pharma & Vaccine clinical trials • Develop and refine templates for consistency, compliance, and strategic study needs • Lead direct negotiations with large academic institutions and other critical stakeholders • Draft and finalize clinical trial agreements balancing business objectives with legal and operational protections • Conduct FMV assessments and site justification reviews when initial offers are declined • Determine when budget or language escalation is needed and secure appropriate approvals • Prioritize and lead multiple contracting projects across several therapeutic areas • Escalate risks, timeline impacts, or delays affecting CTA execution • Maintain accurate and timely updates in departmental trackers and databases • Build relationships with internal and external partners • Support and train additional team members • Contribute to process improvement initiatives • Take on ad-hoc tasks and diverse projects

🎯 Requisitos

• 2+ years of experience in a fast-paced and volume-driven work environment • Direct experience negotiating with large academic institutions • Ability to juggle priorities, lead projects, and deliver results under tight timelines • Strong understanding of clinical study protocols, timelines, and site-related milestones, such as SIV • Bachelor’s degree • Expert proficiency in Excel and clinical trial management systems • Knowledge of GCP, sponsor processes, SOPs, and work instructions • Oncology therapeutic area experience preferred • Prior experience with pharma, CRO, or investigative sites preferred • Strong project management skills and comfort leading cross-functional efforts preferred • Experience leveraging AI in contracts and budgets preferred

🏖️ Benefícios

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Company car or car allowance • Medical, Dental and Vision health benefits • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) • Sick time • Reasonable accommodations, when appropriate • Comprehensive resources including emerging technologies, data, science and knowledge sharing

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