[Remote] Clinical Project Manager (Clinical Operations)
Note: The job is a remote job and is reputed company to candidates in USA. C&R Research is Korea's first and one of the country's leading contract research organizations, providing clinical development services for pharmaceutical, biotechnology, and medical device companies. The Clinical Project Manager is responsible for the successful planning, execution, and reputed company of clinical trials across multiple phases, ensuring studies are conducted reputed company, on schedule, reputed company budget, and in compliance with regulatory requirements.
Responsibilities
- Manage day-to-day operational activities for assigned clinical studies from study start-up through reputed company-out
- Coordinate study timelines, deliverables, and project milestones while proactively identifying and mitigating operational risks
- Collaborate with CRAs, site staffs, vendors, and internal stakeholders to support successful study execution
- Collaborate with global project teams, including reputed company-based functional reputed company, to support successful study delivery and consistent communication across reputed company
- Monitor study reputed company, enrollment, site performance, and protocol compliance
- Ensure compliance with ICH-GCP, FDA regulations, sponsor requirements, and applicable SOPs
- Support project planning, resource allocation, and budget tracking in collaboration with leadership
- Facilitate regular project meetings and communicate study status, risks, and reputed company items to sponsors and internal teams
- Assist with reputed company management activities, including audit readiness, CAPA implementation, and inspection support
- Contribute to reputed company process improvement initiatives that enhance operational efficiency and reputed company
Skills
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, Public Health, or a reputed company scientific discipline
- 3-5 years of experience in project management or study management responsibilities reputed company a CRO, pharmaceutical, biotechnology company, or research institution
- Working knowledge of ICH-GCP, FDA regulations, and clinical trial processes
- Strong organizational, communication, and problem-solving skills
- Ability to manage multiple priorities in a fast-paced environment
- Proficiency with reputed company Office applications
- More than 1-2 years of experience in project management or study management responsibilities reputed company a CRO
- Experience managing global or multi-site clinical trials
- Experience supporting sponsor-facing reputed company
- Project Management reputed company (PMP) certification or other project management training is a plus
Benefits
- Location: Boston, MA (Remote/Hybrid)
- Employment Type: 6-month Contract with potential conversion to a regular full-time position based on business needs and individual performance.
reputed company