Clinical Project Manager

Position Summary: We are seeking an experienced Clinical Project Manager (CPM) with a strong background in respiratory clinical research to oversee the planning, execution, and management of clinical trials. The ideal candidate will have experience managing respiratory studies, collaborating with cross-functional teams, ensuring regulatory compliance, and driving study milestones from start-up through closeout. This individual will serve as the primary point of contact for sponsors, investigators, and study teams while ensuring projects are delivered on time, within budget, and in accordance with GCP, FDA regulations, and company SOPs.

Key Responsibilities: Lead the operational management of respiratory clinical trials from study start-up through closeout. Serve as the primary liaison between sponsors, CROs, investigative sites, and internal teams. Develop and maintain project timelines, study plans, and milestone tracking. Monitor study progress and proactively identify and mitigate project risks. Manage study budgets, timelines, and resource allocation. Coordinate site activation, patient enrollment, monitoring activities, and database lock. Ensure compliance with ICH-GCP guidelines, FDA regulations, protocol requirements, and company SOPs. Oversee vendor relationships, including central laboratories, imaging vendors, and specialty service providers. Facilitate sponsor meetings, project status updates, and cross-functional team meetings. Review study metrics and prepare project reports for sponsors and leadership. Support regulatory submissions and study documentation as needed. Mentor and provide guidance to Clinical Research Coordinators, Clinical Research Associates, and project team members.

Required Qualifications: Bachelor's degree in Life Sciences, Nursing, Public Health, or a related field. Minimum of 3–5 years of clinical project management experience. Previous experience managing respiratory clinical trials (e.g., asthma, COPD, pulmonary fibrosis, cystic fibrosis, or other respiratory indications).Strong knowledge of ICH-GCP, FDA regulations, and clinical research processes. Experience working with EDC, CTMS, eTMF, and other clinical trial management systems. Excellent organizational, communication, and leadership skills. Ability to manage multiple studies simultaneously in a fast-paced environment. Strong problem-solving and decision-making abilities.

Preferred Qualifications: Project Management Professional (PMP) certification or equivalent. Experience working with CROs and pharmaceutical or biotechnology sponsors. Familiarity with pulmonary function testing (PFTs), spirometry, respiratory devices, and respiratory endpoints. Experience managing multicenter clinical trials. Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) certification preferred. Skills Clinical trial management Sponsor relationship management Budget and timeline oversight Risk management Regulatory compliance Team leadership Vendor management Strong Microsoft Office and clinical software proficiency Excellent written and verbal communication skills****Thank you for your interest in this opportunity! Due to the high volume of applications we receive, we are unable to respond to every applicant individually. If you do not hear from us regarding this role, it means we have moved forward with other candidates at this time. We sincerely appreciate your interest and encourage you to apply for future opportunities that match your experience and career goals.