What are the responsibilities and job description for the Senior Project Manager - Clinical Trials position at QPS, LLC?
Job Description
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!
Senior Project Manager – Late Phase Global Clinical Trials
Lead the Future of Clinical Research!
Are you a clinical trial expert with a knack for keeping global projects on track? Do you thrive in a fast-paced, multicultural environment where strategic thinking meets hands-on execution? If so, consider joining QPS as our Sr Project Manager (sPM) !
QPS’ Story :
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
As a Sr. Project Manager (sPM), you’ll be the driving force behind global clinical trials, ensuring they are executed efficiently, within budget, and in compliance with regulatory guidelines. You’ll work closely with regional project managers, vendors, and clients, ensuring seamless communication, risk management, and quality oversight from study start-up to close-out.
What you’ll do :
- Oversee the planning and execution of clinical trials across Phases 1-4.
- Lead study startup activities, including site selection, vendor agreements, and regulatory compliance.
- Manage timelines, budgets, and resources while proactively mitigating risks.
- Train and mentor project managers, clinical trial associates, and cross-functional teams.
- Ensure high-quality deliverables by reviewing site reports, vendor performance, and regulatory documentation.
- Maintain strong relationships with clients, ensuring top-notch service and transparency throughout the project lifecycle.
- Stay “Inspection Ready” by managing deviations, compliance, and quality control measures.
Work Location
This job will be 100% home-office based with occasional travel of up to 10% (see Telecommuting Policy for full details)
Requirements
What you bring :
What we offer
Ready to take the next step in your career? Apply today and be part of a team that's shaping the future of clinical research!
