Sr. Imaging Project Manager

Planet Pharma • scottsdale, az, United States • 3h ago

1

Execute project deliverables for imaging studies in clinical trials in accordance with project scope of work and within sponsor specified timelines;
Manage day-to-day operational aspects of a clinical imaging projects.
Assist in preparation and adherence to imaging trial documents i.e. Image Review Charter, Imaging Manual, Data Transmittal Forms, etc;
Ensure project documents are complete, current, and stored appropriately;
Manage key project documents/processes, i.e. Project Management Plan, Communication Plan, Escalation Plan, Risk Management Plan and appropriate Clinical Trial Management System (CTMS);
Identify resources needed and assign individual responsibilities;
Identify out of scope requests and work with appropriate team(s) to revise the work order to meet changing needs and requirements;
Review and manage all deliverables;
Prepare metrics reporting for client and senior management;
Prepare forecasting information for Finance purposes;
Perform other duties as assigned by the Supervisor

EDUCATION AND EXPERIENCE

Bachelor’s degree or equivalent certification in a health related field
Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is required
Knowledge of key project management documents and tools a must
Prior experience with different EDC systems required
Proficiency in MS Office and internet applications required
Minimum of 3 to 5 years of experience in the clinical trials industry required
Minimum of 2 years of experience in medical imaging in a clinical trial environment required
Experience managing global Phase III clinical trials with imaging components strongly preferred
PMP certification a plus

SKILLS

Service oriented approach, flexible and proactive towards adapting to sponsors’ needs
Ability to manage project activities with diverse groups and individuals
Must have superior attention to detail and excellent oral and written communication skills
Self-driven, ability to get the job done with little supervision, can-do positive attitude
Ability to excel in a team environment
Must have the ability to work under pressure with multiple competing priorities
Must have strong time management, and organizational skills. Prioritizing workload to the changing needs of the day to day business is also a critical skill.
Ability to work in strict compliance with all procedures, rules and regulations
Maintain strict confidentiality of sensitive data, records, files, conversations, etc.
Must be self-motivated and able to grasp new concepts quickly
Possess the ability to understand research projects and successfully lead within the clinical trial environment

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