You have opted out of job matches in .
To undo this, go to the 'Skills and Interests' section of your preferences.
Shared by 
10 days ago
Requirements and responsibilities
About AscendionAscendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees. Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered workforce of 11,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next.Ascendion | Engineering to elevate lifeWe have a culture built on opportunity, inclusion, and a spirit of partnership. Come, change the world with us:Build the coolest tech for world’s leading brandsSolve complex problems - and learn new skillsExperience the power of transforming digital engineering for Fortune 500 clientsMaster your craft with leading training programs and hands-on experienceExperience a community of change makers!Join a culture of high-performing innovators with endless ideas and a passion for tech. Our culture is the fabric of our company, and it is what makes us unique and diverse. The way we share ideas, learning, experiences, successes, and joy allows everyone to be their best at Ascendion.About the Role:We are hiring an experienced Technical Program Manager to support a high-visibility clinical trial data program for a confidential enterprise client in the technology space. This is a hands-on, high-ownership role for someone who has run clinical trial programs before - not observed or supported them - and who understands the full lifecycle of clinical trial data, from raw data capture through FDA-submittable output.Key Responsibilities:Own end-to-end program management for a clinical trial data workstream, including planning, tracking, and delivery against milestones.Manage the clinical trial data lifecycle - from raw/source data through cleaning, validation, and structuring to FDA-submittable format.Rapidly assess current program status, identify gaps, risks, and blockers, and take direct action to resolve them.Partner closely with a client-side program manager as a true peer - proactively taking on workload, not waiting for delegation.Serve as a direct interface to the client, representing program status, risks, and priorities in client conversations without requiring a middle layer of translation or oversight.Manage day-to-day program tracking and ticket workflow uring visibility into status, ownership, and progress across workstreams.Coordinate across internal and vendor/technical teams to ensure data workflows, timelines, and quality standards are met.Track and report program progress, surfacing risks early with proposed solutions, not just statusMinimum Qualifications:Hands-on experience managing a clinical trial program (not adjacent experience - direct, prior ownership of a clinical trial program required).Deep understanding of clinical trial data workflows, including raw data intake, cleaning/validation, structuring, and progression to FDA-submittable stage.Direct client-facing experience - proven track record interfacing directly with clients or senior stakeholders, not just internal teams.Asana fluency - hands-on, day-to-day experience managing tickets, tasks, and program tracking in Asana (not just general PM tool familiarity).Proven ability to operate with high autonomy - able to walk into an ambiguous or in-flight program and start contributing immediately.Strong program/project management fundamentals: planning, milestone tracking, risk management, resource coordination.Demonstrated ownership mentality - someone who has a track record of taking on problems beyond their explicit scope because it served the outcome.Prior experience specifically in FDA-regulated clinical trial submission processesExperience working as a vendor/consulting partner embedded within a large enterprise client teamHands on experience with clinical data standards (e.g., CDISC, SDTM)Desired Qualifications:Should have direct experience managing a clinical trial program as well as managing Software teams.Some one who can bridge as a program manager translating SME terms to software equivalent terms and vice versaBenefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, long-term disability insurance, short-term disability insurance, 5 personal days accrued each calendar year (The Paid time off benefits meet the paid sick and safe time laws that pertains to the City/ State), 10-15 days of paid vacation time, 6 paid holidays and 1 floating holiday per calendar year, Ascendion Learning Management SystemWant to change the world? Let us know.Tell us about your experiences, education, and ambitions. Bring your knowledge, unique viewpoint, and creativity to the table. Let’s talk!