Clinical Country Site Lead – Southwest

🕒 il y a 17 jours

🌵 Arizona, Colorado, +1 états de plus – Distant

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💵 $134 000 - $179 000 / an

⏰ Temps Plein

🟠 Senior

🦅 Parrain de Visa H1B

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👻 Score fantôme 0%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Biogen

Biogen

5001 - 10000 employés

🏥 Santé

🏭 Fabrication

🧬 Biotechnologie

Healthcare • Manufacturing • Biotechnology

Biogen est une entreprise de biotechnologie dédiée à la découverte, au développement et à la délivrance de thérapies innovantes pour les personnes vivant avec des maladies neurologiques graves, telles que la maladie d'Alzheimer, la sclérose en plaques et l'atrophie musculaire spinale. Avec un fort accent sur la recherche et le développement, Biogen continue de faire progresser la science de la neurologie grâce à des essais cliniques et des partenariats stratégiques, tout en s'efforçant d'assurer l'accès aux soins et l'équité en matière de santé.

Description

• 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

🎯 Exigences

• 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

🏖️ Avantages

• 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

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