
5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Biogen is a biotechnology company dedicated to discovering, developing, and delivering innovative therapies for people living with serious neurological diseases, including Alzheimer's disease, multiple sclerosis, and spinal muscular atrophy. With a strong emphasis on research and development, Biogen continues to advance the science of neurology through clinical trials and strategic partnerships, while also striving for access and health equity in healthcare.
🔥 0 minutes ago
🌵 Arizona, Colorado, +1 more states – Remote
💵 $134k - $179k / year
⏰ Full Time
🟠 Senior
🦅 H1B Visa Sponsor
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5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Biogen is a biotechnology company dedicated to discovering, developing, and delivering innovative therapies for people living with serious neurological diseases, including Alzheimer's disease, multiple sclerosis, and spinal muscular atrophy. With a strong emphasis on research and development, Biogen continues to advance the science of neurology through clinical trials and strategic partnerships, while also striving for access and health equity in healthcare.
• 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
• 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
• 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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