Sr. Clinical Project Manager
location_on2173;2189, Washington Street, Nubian Square, Roxbury, Boston, Suffolk County, Massachusetts, 02119, United States
Job Description
About the Opportunity
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. We are currently seeking a dedicated Senior Clinical Project Manager to join a client team in Boston, MA. This is a fully remote contract position offering the flexibility to work from anywhere while leading the planning and execution of large, global clinical trials in oncology.
The Role
As a Senior Clinical Project Manager, you will provide operational leadership within clinical development. Your primary focus will be managing project teams to ensure that timelines and budgets are met for complex global studies. You will oversee study execution, including the management of CROs, vendors, and consultants, ensuring that milestones are met and metrics are tracked effectively.
This role requires strong communication and collaboration skills, as you will guide investigator recruitment, ensure staff training on guidelines and SOPs, and provide mentoring to junior team members. You will also be responsible for maintaining the Trial Master File, responding to Quality Assurance audits and regulatory inspections, and contributing to clinical documentation and regulatory submissions.
Application Process
If you are interested in this exciting opportunity, please click 'Apply' or request a callback to speak with one of our specialists. If you have any questions or are experiencing difficulty applying, please contact Bodin Forsen at b.forsen@proclinical.com.
Equal Opportunity
Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you have read and understood our privacy policy, which informs you how we process and safeguard your data.
Work location
Work model: Remote
2173;2189, Washington Street, Nubian Square, Roxbury, Boston, Suffolk County, Massachusetts, 02119, United States
Boston, Massachusetts
Key Responsibilities
- check_circleLead planning and execution of large, global clinical trials in oncology
- check_circleManage project teams to ensure timelines and budgets are met
- check_circleOversee study execution and management of CROs, vendors, and consultants
- check_circleManage individual study projects, ensuring milestones are met and metrics tracked
- check_circleLead risk management efforts and report progress to senior leadership
- check_circleGuide investigator recruitment and ensure staff training on guidelines and SOPs
- check_circleEnsure compliance with ICH-GCP, federal, and local regulations
- check_circleContribute to clinical documentation and regulatory submissions
- check_circleMaintain responsibility for study-related operational plans and quality management
- check_circleParticipate in forecasting and managing clinical trial supplies
- check_circleEnsure proper maintenance of the Trial Master File
- check_circleRespond to Quality Assurance audits and regulatory inspections
Requirements
- verifiedBachelor's degree in health sciences or related field
- verifiedExperience in clinical research and study management
- verifiedProficient in managing CROs, vendors, and consultants
- verifiedKnowledge of FDA Regulations and ICH-GCP guidelines
- verifiedTherapeutic knowledge in oncology preferred
- verifiedProficient in Excel, Word, PowerPoint, Outlook, and MS Project
- verifiedAbility to travel as needed
Skills, education and keywords
Skills: excel, word, powerpoint, outlook, ms project, oncology, clinical research, study management, ich-gcp, fda regulations.
Education: Bachelor's degree in health sciences or related field required.