via Workday
$90K - 110K a year
Lead and manage client projects in clinical trials, including planning, monitoring, budgeting, risk mitigation, and stakeholder communication.
Bachelor's degree, 3-5 years project management in pharmaceutical or related industry, Clario PM Certification required, PMP preferred, strong organizational and communication skills, ability to travel up to 20%.
At Clario, we’re transforming lives by unlocking better evidence. As a Project Manager II, you’ll lead critical client projects in the neuroscience space, ensuring high-quality, on-time, and on-budget delivery while fostering collaboration and exceptional customer service. Your expertise will help accelerate clinical research and improve patient outcomes. What We Offer Competitive compensation Comprehensive medical, dental, and vision coverage Paid time off and flexible work options Wellness programs and tuition reimbursement Opportunities for career growth in a global organization What You’ll Be Doing Direct and manage client projects across planning, setup, monitoring, and closeout phases Gather customer requirements and translate them into actionable plans for internal teams Develop study documentation, distribute and track equipment, and manage data archiving Monitor timelines and financial components including budget reviews, revenue forecasting, scope changes, and invoice reconciliation Identify risks, implement mitigation strategies, and escalate issues as needed Serve as the primary point of contact for operational readiness on new product initiatives Apply problem-solving strategies to resolve customer issues and maintain issue tracking documentation Present study services at Investigator Meetings or site initiation meetings as required Support Business Development by attending client meetings and contributing to sales initiatives Assist with onboarding and training new Project Management team members What We Look For Bachelor’s degree or equivalent experience in project management within the pharmaceutical or related industry 3–5 years of project management experience with emphasis on clinical trials Clario PM Certification required; PMP preferred Strong knowledge of the pharmaceutical drug development process and eCOA solutions Excellent organizational, interpersonal, and communication skills Proficiency in Microsoft Office; ability to manage multiple priorities effectively Detail-oriented with demonstrated responsiveness and problem-solving skills Valid passport and ability to travel up to 20% At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster. EEO Statement Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic. Clario Privacy Policy Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere™, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clario’s global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.
This job posting was last updated on 12/5/2025