Clinical Project Manager

Date Posted: 05/27/2026Hiring Organization: Rose InternationalPosition Number: 501812Industry: HealthcareJob Title: Clinical Project ManagerJob Location: Skaneateles Falls, NY, USA, 13153Work Model: OnsiteShift: Monday to Friday, 8 to 5Employment Type: TemporaryFT/PT: Full-TimeEstimated Duration (In months): 8Min Hourly Rate($): 80.00Max Hourly Rate($): 100.00Must Have Skills/Attributes: Clinical, Data Analysis, Program management, RegulatoryExperience Desired: End-to-end clinical study experience (10 yrs); Proactive, collaborative, and self-driven (10 yrs); clinical research experience, including Clinical Project Manager (10 yrs)Required Minimum Education: Bachelor’s DegreeJob DescriptionRequired Education Bachelor's degree in a scientific fieldRequired Skills Clinical Research Experience: 4–5 years of clinical research experience (including 1–2+ years as a Clinical Project Manager) Regulatory Knowledge: Knowledge of FDA, ICH/GCP, and global regulatory requirements Clinical Trials: Understanding of clinical trial phases (Phase 1–4) Clinical Systems: Experience with clinical systems (EDC, CTMS, eTMF) Project Management: Strong project management skills Cardiac Knowledge: Knowledge of arrhythmias, ECG interpretation, or ambulatory cardiac monitoring systems Data Interpretation: Ability to interpret diagnostic performance metrics (e.g., sensitivity, specificity, PPV/NPV) and translate findings into clinical insights Risk Assessment: Experience assessing risk/benefit and clinical implications of algorithm performance differences Algorithm/Device Knowledge: Familiarity with algorithm-based diagnostics or AI/ML-driven medical devices Regulatory Validation: Understanding of validation requirements for medical devices (e.g., EU MDR, FDA expectations) Soft Skills: Proactive, collaborative, and self-driven with a take-charge attitudeJob Responsibilities Partner with relevant Baxter functions to develop clinical study plan for each project including timelines and budgets for the clinical program Prepare directly or facilitate preparation of study documentation including protocols, case report forms, informed consent, enrollment feasibility evaluations, and all relevant internal plans required for study conduct CRO Management (when applicable): Lead the day-to-day oversight of the CRO personnel plus the project budget, deliverables, and timeline/milestones Site Activities (either directly or managing others): Identify and assess study sites, conduct investigator meetings and site training, prepare and execute research agreements, and negotiate study budgets Study Monitoring (either directly or managing others): Formulate clinical monitoring plan, perform study initiation visits, manage clinical study monitoring resources, oversee standard interim monitoring visits and closeout activities Perform study closeout procedures, directly or through other resources, including accurate completion of critical documents, disposition of study product, and preparation of study sites for regulatory authority audits Develop and maintain tracking systems as needed for study management (e.g., screening, enrollment, study completion, serious adverse events, budgets and forecasts, milestones)BenefitsFor information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay EquityFor information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).