
10.000+ Mitarbeiter
Gegründet 1886
🏥 Gesundheitswesen
⚕️ Krankenversicherung
💊 Pharmazie
Healthcare • Healthcare Insurance • Pharmaceuticals
Johnson & Johnson ist ein globales Gesundheitsunternehmen, das Arzneimittel, Therapien und medizinische Geräte in verschiedenen therapeutischen Bereichen entdeckt, entwickelt, herstellt und vermarktet, darunter Onkologie, Neurowissenschaften, Immunologie, Herz-Lungen- und Herz-Kreislauf-Versorgung, Orthopädie, Chirurgie und Augenheilkunde. Das Unternehmen betreibt groß angelegte Forschungs- und Entwicklungsprogramme, klinische Entwicklungs- und Fertigungsprogramme und ist auch aktiv in Mitarbeiterprogrammen, Nachhaltigkeit, globalen Gesundheitsinitiativen und gesellschaftlichem Engagement weltweit.
🕒 vor 4 Tagen
🔔 Pennsylvania – Remote
💵 $92.000 - $148.350 / Jahr
⏰ Vollzeit
🟠 Senior
⚙️ Operations
🦅 H1B-Visum-Sponsor
👻 Geisterscore 0%
🗣️🇺🇸🇬🇧 Englisch erforderlich
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10.000+ Mitarbeiter
Gegründet 1886
🏥 Gesundheitswesen
⚕️ Krankenversicherung
💊 Pharmazie
Healthcare • Healthcare Insurance • Pharmaceuticals
Johnson & Johnson ist ein globales Gesundheitsunternehmen, das Arzneimittel, Therapien und medizinische Geräte in verschiedenen therapeutischen Bereichen entdeckt, entwickelt, herstellt und vermarktet, darunter Onkologie, Neurowissenschaften, Immunologie, Herz-Lungen- und Herz-Kreislauf-Versorgung, Orthopädie, Chirurgie und Augenheilkunde. Das Unternehmen betreibt groß angelegte Forschungs- und Entwicklungsprogramme, klinische Entwicklungs- und Fertigungsprogramme und ist auch aktiv in Mitarbeiterprogrammen, Nachhaltigkeit, globalen Gesundheitsinitiativen und gesellschaftlichem Engagement weltweit.
• Own US site-level operational delivery for assigned sites and trials from feasibility through closeout • Support and coordinate local trial team activities in compliance with SOPs, procedural documents, and applicable regulations • Plan local trial activities to meet recruitment targets and deliver high-quality data on time and within budget • Develop local trial-specific procedures and tools • Lead recruitment planning, contingency and risk management, and budget forecasting • Provide functional guidance and mentoring to Local Operations Managers when appropriate • Contribute to US trial operational strategy and integrate site insights into global feasibility and startup planning • Serve as the primary US operational interface to global trial leadership when assigned • Monitor country-level operational KPIs and identify systemic risks and mitigation strategies • Support escalation and resolution of complex site contracting, operational, and recruitment issues • Collaborate with Leads and cross-functional partners • Represent US local operations at investigator and study coordinator site meetings and governance forums • Act as subject matter expert for assigned protocols and develop therapeutic knowledge • Represent Oncology Site Enablement on cross-functional teams when assigned • Elevate US site insights to inform global decision-making and continuous improvement • Lead or represent country, Delivery Unit, and global process initiatives and special initiatives such as Champion or Subject Matter Expert
• A minimum of a bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline (or equivalent experience) is required • Minimum of 2 years of experience in clinical trial operations, trial management, site management, or clinical monitoring, including significant experience in complex, high-priority, or multi-site trials • Demonstrated experience in oncology trial operations is strongly preferred • In-depth understanding of the clinical development process and end-to-end trial delivery • Expertise in feasibility, startup strategy, enrollment execution, quality oversight, and closeout • Strong knowledge of GCP, regulatory requirements, inspection readiness, and compliance management • Experience supporting audits and regulatory inspections • Experience shaping or contributing to country-level or trial-level operational strategy, including site selection, enrollment forecasting, and risk mitigation planning • Strong analytical skills to interpret country- and site-level KPIs, identify systemic risks, and implement corrective actions • Excellent written and verbal communication skills in both the local country language and English • Willingness to travel up to 10%, including overnight stays and participation in investigator meetings and key trial governance meetings • Demonstrated flexibility, resilience, and ability to operate effectively in a highly complex, fast-changing clinical development environment
• Consolidated retirement plan (pension) • Savings plan (401(k)) • Long-term incentive program • Vacation – 120 hours per calendar year • Sick time – 40 hours per calendar year; 48 hours per calendar year for employees residing in Colorado; 56 hours per calendar year for employees residing in Washington • Holiday pay, including Floating Holidays – 13 days per calendar year • Work, Personal and Family Time – up to 40 hours per calendar year • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child • Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year • Caregiver Leave – 80 hours in a 52-week rolling period • 10 days Volunteer Leave – 32 hours per calendar year • Military Spouse Time-Off – 80 hours per calendar year • Inclusive interview process and accommodation support
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