Sr Clinical Data Project Manager

Location: Remote, US   About This Role: Veranex is seeking a Senior Clinical Data Project Manager to lead the delivery of high-impact clinical data initiatives supporting innovative medical technologies. This is a strategic, client-facing role responsible for driving execution excellence across the full clinical data lifecycle — from study start-up through closeout. You will serve as the central point of accountability for clinical data project performance, ensuring scope, timelines, quality standards, and client expectations are consistently met or exceeded. This role requires a strong command of biometrics operations, cross-functional leadership capability, and the ability to proactively mitigate risk in a fast-paced, innovation-driven environment. If you thrive at the intersection of clinical science, data integrity, and client partnership, this role offers meaningful impact and visibility within a growing global MedTech organization.   What You Will Do: Serve as the primary client liaison for assigned clinical data programs, managing contractual obligations, project governance, and stakeholder expectations Lead cross-functional clinical data teams, aligning resources and ensuring optimal performance across biometrics functions Develop and manage comprehensive project plans covering scope, schedule, budget, risk, and quality Ensure compliance with Good Clinical Practices (GCP), regulatory requirements, and internal SOPs Identify project risks early and implement mitigation and corrective/preventative action plans as needed Oversee quality management processes to ensure data integrity and inspection readiness Drive transparent communication through accurate and timely status reporting and executive-level updates Support client retention and business growth through strong project execution and relationship management   Qualifications Required skills: Bachelor’s or Master’s degree or international equivalent in Life Sciences Bachelor’s degree or international equivalent and 3-7 years of relevant work experience, or Master’s degree or international equivalent and 2-6 years of relevant work experience Strong knowledge of clinical trial life cycle from start-up to closeout Demonstrated knowledge of regulatory compliance requirements and GCP Solid understanding of clinical data management and biometrics functions Proven ability to manage scope, timelines, and competing priorities across multiple projects Experience leading and coordinating cross-functional teams Strong organizational skills and attention to detail Preferred: Experience in the medical device industry highly preferred