Senior Clinical Project Manager

🔥 14 hours ago

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $135.5k - $216.8k / year

⏰ Full Time

🟠 Senior

🏥 Clinical Operations

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This company has sponsored H1B visas in the past.

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BD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1897

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

💰 $24M Grant on 2020-07

Healthcare • Manufacturing • Healthcare Insurance

BD (Becton, Dickinson and Company) is a global medical technology company dedicated to advancing the world of health. It focuses on developing innovative technologies, services, and solutions to improve safety and efficiency in healthcare. BD offers a wide range of products including medication management solutions, surgical solutions, cervical cancer screening, drug delivery systems, and laboratory services. The company is also involved in infection risk management and provides advanced clinical insights to enhance patient outcomes. With a commitment to global health sustainability and social investing, BD is a leader in healthcare technology and services worldwide.

📋 Description

• Prepare and/or review study-related and essential study start-up documents for assigned clinical trials • Serve as Clinical Project Manager and ensure Study Management teams meet study timelines and deliverables • Oversee and lead study-specific study management resources • Develop and manage groups of studies for a business unit or large development program • Mentor other Clinical Project Managers • Provide critical thinking and leadership during clinical study execution issues • Write protocols, clinical study reports, and other clinical study deliverables • Lead or contribute to continuous improvement initiatives • Manage relationships with sites, principal investigators, CROs, and other study-related vendors • Develop and maintain integrated project plans and facilitate project meetings • Define, track, and report schedules, interdependencies, achievements, critical paths, and deliverables • Adapt work package deliverables based on study scale and complexity • Create resource and budget forecasts and timelines • Direct cross-functional team members and vendors on technical, protocol-specific, and operational study aspects • Identify and manage project risks and issues, including mitigations and contingencies • Maintain high-quality standards and compliance requirements • Perform other assigned duties

🎯 Requirements

• Bachelor's degree, preferably in the life sciences, clinical, or other relevant technical areas • Minimum of 5 years of clinical study experience in pharmaceutical, medical device, IVD, biotechnology, or CRO environments • Proven ability to lead cross-functional clinical teams through complex, global, multicenter studies from initiation through closeout • Minimum of 5 years of project management experience, preferably using MS Project • Strong knowledge of clinical trial concepts, international clinical research guidelines, and regulatory requirements • Hands-on experience managing Trial Master Files (TMF) in compliance with ICH-GCP and regulatory standards • Ability to influence cross-functional teams without formal authority • Financial acumen, including project budgeting, financial forecasting, and strategic recommendations • Strong project management, client relationship, and vendor relationship management skills • Ability to work independently with multi-level teams and manage multiple projects in a fast-paced, changing environment • Exceptional written and verbal communication, interpersonal, negotiation, and relationship-management abilities • Expert-level knowledge of clinical operations procedures • Exceptional problem-solving, organizational, analytical, and critical-thinking abilities • Strong leadership skills • Proficiency in Microsoft Office Suite, including expert-level Excel skills with Pivot Tables and VLOOKUP • Proven ability to work effectively in a remote environment • Ability to travel approximately 20% and reside near a major airport • Advanced degree desirable, including MS, MBA, PhD, MPH, PharmD, or MD • PMP certification highly desirable • Technical and/or medical writing experience desired

🏖️ Benefits

• Comprehensive Total Rewards program • Reward and recognition opportunities • Competitive compensation and benefits programs • Flexible work-life balance considerations • Remote or field-based workplace arrangements as indicated • Learning, growth, and development opportunities • COVID-19 vaccination accommodation consideration pursuant to applicable law