Senior Clinical Project Manager – NIH/NCI Trials & Informatics

CAMRIS; Rockville (MD); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical insurance

401(k) with employer match

Tuition reimbursement

Paid time off

Job summary

CAMRIS International seeks a Clinical Project Manager II to support NIH/NCI initiatives in Rockville, MD. The role emphasizes clinical trial reporting, biomedical informatics, data management, and operations, with engagement across CTRP/CTRO, PRS, and EVS terminology.

You will lead cross-functional teams, manage schedules and budgets, and ensure regulatory reporting and quality assurance, working with government and academic partners. The position is forecasted pending contract award.

Qualifications

• Bachelor's degree in clinical research, life sciences, health sciences, biomedical informatics, public health, IT, or related.
• Minimum 5 years of experience in clinical operations, data management, or biomedical informatics.

Responsibilities

• Lead planning, execution, monitoring, reporting, and coordination of clinical trial and biomedical informatics activities.
• Manage project schedules, scope, risks, issues, deliverables, budgets, and stakeholder communications.
• Coordinate cross-functional clinical, scientific, technical, regulatory, and data-management teams.
• Support CTRP/CTRO operations, including trial registration, status updates, QA, and SOP development.
• Apply project-management best practices across initiation, planning, execution, control, and closeout.

Skills

Project management

Stakeholder management

Regulatory reporting

Clinical trial lifecycle

Cross-functional coordination

Education

Bachelor's degree in clinical research or related field

Tools

NCI CTRP/CTRO

NCI ClinicalTrials.gov PRS

NCI Thesaurus/EVS

Job description

CAMRIS International seeks a Clinical Project Manager II to support NIH/NCI initiatives in Rockville, MD. The role emphasizes clinical trial reporting, biomedical informatics, data management, and operations, with engagement across CTRP/CTRO, PRS, and EVS terminology.

You will lead cross-functional teams, manage schedules and budgets, and ensure regulatory reporting and quality assurance, working with government and academic partners. The position is forecasted pending contract award.