via Workday
$80K - 130K a year
Ensure operational excellence and client satisfaction across complex clinical trial programs, monitor study timelines and budgets, and lead cross-functional teams.
Bachelor’s degree or equivalent, 4-8 years in pharmaceutical or related industry, proven leadership skills, knowledge of drug development process, excellent communication, and ability to travel.
Clario is a global leader in clinical trial endpoint technology solutions, transforming lives by unlocking better evidence. As a Program Manager, you will ensure operational excellence and client satisfaction across complex programs of work. Join us and help accelerate the future of clinical trials through innovation and collaboration. What We Offer Competitive compensation Medical, dental, and vision coverage starting Day 1 Flexible work schedules and attractive PTO plan Remote work options Engaging employee programs What You’ll Be Doing Ensure consistency of delivery across programs by setting standards, sharing lessons learned, and communicating client-specific requirements to internal teams Serve as a member of Oversight/Operations Committees for assigned clients Partner with clients and internal teams to review study risks, mitigation plans, and opportunities for improved delivery, profitability, and quality Monitor study timelines and manage financial components across assigned accounts Identify and escalate potential study risks, driving timely resolution Foster collaboration through effective negotiations and resource management to meet timelines and contractual obligations Apply problem-solving strategies to address customer issues and maintain issue tracking documentation Monitor and report program-level KPIs as needed Attend operational and governance meetings with customers (in-person and remote) Support cross-trained team members, influence strategic decisions, and ensure compliance with training requirements Present study services at sponsor-related meetings and assist with training new Project Management team members What We Look For Bachelor’s degree or equivalent practical experience 4–8 years of experience in the pharmaceutical or related industry, with emphasis on project management Proven ability to mentor staff and lead cross-functional teams Knowledge of the drug development process Excellent organizational, interpersonal, and time management skills Strong verbal and written communication skills in English Proficiency in Microsoft Office products Detail-oriented with responsiveness to inquiries and requests Valid passport and ability to travel approximately 20% Based in or able to work remotely within the United States 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 is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.
This job posting was last updated on 12/13/2025