Clinical Country Site Lead – Southwest

🕒 5 dias atrás

🌵 Arizona, Colorado, +1 estados a mais – Remoto

🌵 Arizona – Remote ⛰️ Colorado – Remote 🤠 Texas – Remote

💵 $134.000 - $179.000 / ano

⏰ Tempo Integral

🟠 Sênior

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Biogen

SiteLinkedInTodas as Vagas

5001 - 10000 funcionários

🏥 Saúde

🏭 Manufatura

🧬 Biotecnologia

Healthcare • Manufacturing • Biotechnology

A Biogen é uma empresa de biotecnologia dedicada à descoberta, desenvolvimento e fornecimento de terapias inovadoras para pessoas que vivem com doenças neurológicas graves, incluindo a doença de Alzheimer, esclerose múltipla e atrofia muscular espinhal. Com forte ênfase em pesquisa e desenvolvimento, a Biogen continua a avançar na ciência da neurologia por meio de ensaios clínicos e parcerias estratégicas, enquanto também se esforça para garantir acesso e equidade em saúde no setor de saúde.

Descrição

• Support and manage Biogen's internalized flexible model, collaborating with Clinical Monitoring Leads, CRAs, FSP partners, and FSO-model partners • Maintain current local knowledge of therapeutic areas and clinical trial requirements • Provide country-level operational and scientific information for studies and programs • Drive global operational strategy by delivering study information • Manage investigator and research-site relationships • Lead local country and site selection activities and incorporate local stakeholder feedback • Serve as primary contact for strategic development and sponsor oversight of CRO activities • Oversee Sponsor Oversight Visits, audits, and inspections for regulatory compliance • Monitor trial progress, resolve local challenges, and align with global teams • Act as Lead CCSL for study or program leadership, including training and coordinating site selection activities • Build relationships across the organization while operating remotely

🎯 Requisitos

• Bachelor's Degree with a science background and experience required • 8+ years of clinical research experience • Experience managing clinical trial activities, especially sponsor oversight with CROs/vendors • Understanding of cross-functional drug development processes • Scientific/clinical knowledge across key therapeutic areas • Familiarity with ICH/GCP and country regulations • Strong organizational and project management skills • Proficiency in relevant IT tools for virtual teamwork • Excellent knowledge of clinical operational activities in the local geography • Strong communication skills, including English proficiency in non-English-speaking countries • Willingness to travel 50–75% (2–3x/month) • Leadership and interpersonal skills preferred • Collaborative decision-making approach preferred • High emotional intelligence and cultural awareness preferred

🏖️ Benefícios

• Short-term and long-term incentives, including cash bonus and equity incentive opportunities • Medical, Dental, Vision, & Life insurances • Fitness & Wellness programs including a fitness reimbursement • Short- and Long-Term Disability insurance • Minimum of 15 days of paid vacation • Additional end-of-year shutdown time off (Dec 26-Dec 31) • Up to 12 company paid holidays + 3 paid days off for Personal Significance • 80 hours of sick time per calendar year • Paid Maternity and Parental Leave benefit • 401(k) program participation with company matched contributions • Employee stock purchase plan • Tuition reimbursement of up to $10,000 per calendar year • Employee Resource Groups participation • Opportunities for learning, growth, and expanding skills