Lead Local Operations Manager – Oncology, Hematology

Job not on LinkedIn

🔥 59 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

💵 $109k - $174.8k / year

⏰ Full Time

🟠 Senior

⚙️ Operations

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Johnson & Johnson

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare • Pharmaceuticals • Biotechnology

<Johnson & Johnson> is a global healthcare company that researches, develops, manufactures and markets pharmaceuticals, medical devices and consumer health products. The company focuses on innovative medicines and therapies across oncology, immunology, neuroscience and cardiopulmonary areas, and develops MedTech solutions in cardiovascular, orthopaedics, surgery and vision. Johnson & Johnson also engages in health & wellness education, large-scale manufacturing, investor activities and global social-impact initiatives.

📋 Description

• Owns US site level operational delivery for assigned sites • Leads and coordinates local trial team activities in compliance with SOPs, other procedural documents, and applicable regulations. • Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget, including but not limited to: development of local trials specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. • Provides leadership oversight and mentoring support to other local operations managers assigned to the trial or program • Shapes US trial operational strategy and integrates site insights into global feasibility and startup planning. • Serves as the primary US operational interface to global trial leadership. • Monitors country level operational KPIs and identifies systemic risks and mitigation strategies. • Acts as escalation point for complex site contracting, operational, and recruitment issues. • Represents US local operations at investigator and/or study coordinator site meetings and key governance forums. • Acts as subject matter expert for assigned protocols and develops strong therapeutic knowledge to support roles and responsibilities. • May represent Oncology Site Enablement on cross functional teams. • Elevates US site insights to inform global decision-making and continuous improvement.

🎯 Requirements

• A minimum of a bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related scientific discipline (or equivalent experience) is required; advanced scientific or clinical degrees are an advantage. • Typically, a minimum of 4 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, with demonstrated expertise in feasibility, startup strategy, enrollment execution, quality oversight, and closeout. • Strong and applied knowledge of GCP, regulatory requirements, inspection readiness, and compliance management, with experience supporting audits and regulatory inspections. • Demonstrated leadership experience, including coaching, mentoring, and guiding other Local Operations Managers or site-facing roles in a player-coach capacity. • Proven ability to lead through influence, resolve escalations, and drive alignment across cross-functional and global trial teams. • Experience shaping or contributing to country-level or trial-level operational strategy, including site selection, enrollment forecasting, and risk mitigation planning. • Strong analytical skills with the ability 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, with demonstrated ability to represent the country or region in global forums. • Willingness to travel up to 10% as required, 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

• medical • dental • vision • life insurance • short and long-term disability • business accident insurance • group legal insurance • consolidated retirement plan • savings plan (401(k)) • vacation –120 hours per calendar year • sick time - 40 hours per calendar year • 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