Director, Clinical Science, Cronos

Job Title: Director, Clinical Science, Cronos Job Location: Bethlehem, United States of America Job Location Type: Home-based Job Contract Type: Full time Job Seniority Level: Director – Clinical Science, Cronos Overview IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences and healthcare industries. Powered by IQVIA Connected Intelligence™, the company brings together high‑quality healthcare data, healthcare‑grade AI, advanced analytics, and deep domain expertise to help customers accelerate innovation, improve patient outcomes, and advance population health worldwide. With a global workforce operating across more than 100 countries, IQVIA is committed to driving smarter healthcare for everyone, everywhere. Cronos is IQVIA’s global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials. Cronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes. To support our clients and uphold the strong reputation Cronos has built for scientific rigor and delivery excellence, we are committed to recruiting, developing, and supporting driven individuals with a combination of clinical, operational, and problem‑solving skills relevant to clinical outcome assessment and rater services. Joining Cronos offers a rewarding and progressive career in patient‑focused clinical research, with opportunities to work on complex, high‑impact studies across multiple geographies. Team members play a hands‑on role in shaping, delivering, and continuously improving solutions that enhance data quality and endpoint reliability. We operate in a truly global, collaborative, and inclusive environment that emphasizes learning, professional growth, and shared success. Role & Responsibilities The Cronos Clinical Science team provides scientific oversight and expertise to ensure the quality, consistency, and reliability of clinical outcome assessment data in global clinical trials. The team supports rater training and calibration, reviews assessment data, identifies and addresses measurement risk, and partners closely with Study Operations and Technology to promote standardized administration, regulatory compliance, and high‑quality endpoints across studies. As a Director in the Cronos Clinical Science team, your responsibilities will include: - Oversee an assigned portfolio of projects. - Lead teams of highly trained clinicians and mentor junior team members. - Supervise and support quality control processes and clinical deliverables, serving as a point of escalation. - Ensure Clinical Team escalations are managed appropriately and in consultation with other departments when needed. - Build and maintain effective relationships with sponsor teams, including attending regular sponsor meetings as required. - Attend and present at Investigators’ Meetings, as assigned. - Review study protocols and provide clinical feedback as appropriate. - Develop methodologies to support study-specific objectives. - Collaborate and build relationships with cross-functional teams in a matrix organization. - Use expertise to propose novel initiatives and process efficiencies, driving process improvement and related activities. - Take ownership of designated processes and/or services. - Identify and present issues and trends in study data. - Provide feedback to clinical trial raters via calls and/or emails, as required. - Develop interven