Social network you want to login/join with: Under limited supervision, assists the Clinical Affairs Manager with the management of clinical studies in accordance with applicable domestic and international regulations, Clinical Investigation Plans, and Standard Operating Procedures. Assists with developing clinical trial strategies, preliminary project timelines, and budgets to ensure successful product development and global marketing efforts. The Clinical Project Manager primarily supports study design, coordination, management, and collaboration with clinical support resources such as monitors, CRAs, Field Clinical Managers, and CROs. Provides clinical support to Sales and Marketing as needed. Works closely with the Clinical Affairs Manager to improve methods by developing or modifying departmental procedures, systems, and training to ensure regulatory compliance. ESSENTIAL JOB FUNCTIONS: Includes but is not limited to: Clinical Management Responsibilities: Coordinate project team meetings Assist in developing clinical study strategies Contribute to study design and protocol development Prepare, review, and distribute study plans, agreements, consent forms, and materials Assist with regulatory submissions, amendments, and communication with authorities Support site selection and establish contact with investigators and staff Oversee study documentation and monitor compliance Assist with data review, safety monitoring, and study closeout activities Project Management: Manage study timelines, budgets, and deliverables Apply project management principles to clinical studies Track project variances and suggest improvements Knowledge, Skills, and Abilities: Proficiency in MS Office and clinical data management systems Ability to work cross-functionally and independently Strong interpersonal and communication skills Knowledge of international regulations (ISO 14155, GCP, GDPR, FDA) Fluency in English; additional languages are a plus Experience: 2-3 years in clinical research, preferably in Medical Devices CRA background and monitoring experience Education: Bachelor’s or higher degree in medical, biological, bio-engineering, or RN qualification J-18808-Ljbffr