Senior Local Operations Manager – Solid Tumor Oncology

Job not on LinkedIn

🔥 0 minutes ago

🔔 Pennsylvania – Remote

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💵 $92k - $148.3k / year

⏰ Full Time

🟠 Senior

⚙️ Operations

🦅 H1B Visa Sponsor

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👻 Ghost score 0%

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Logo of Johnson & Johnson

Johnson & Johnson

10,000+ employees

Founded 1886

🏥 Healthcare

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Healthcare • Healthcare Insurance • Pharmaceuticals

Johnson & Johnson is a multinational corporation focused on innovating across multiple sectors of healthcare and medicine. With a commitment to redefining healthcare, the company merges science and technology to address complex diseases through its divisions in innovative medicine and medical technology. Its areas of focus include oncology, immunology, neuroscience, and specialty ophthalmology, as well as interventional solutions and orthopaedics. J&J is dedicated to advancing global health equity and environmental sustainability while fostering innovation, diversity, and inclusion in the workplace. The company strives to provide solutions that connect health and care for providers, patients, and communities worldwide.

📋 Description

• 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

🎯 Requirements

• 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

🏖️ Benefits

• 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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