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Planet Pharma · 3 days ago

Sr. Project Manager

United States

Full-time

Remote

Mid, Senior Level

3+ years exp

Planet Pharma is a company focused on advancing clinical trials, and they are seeking a Senior Project Manager to oversee imaging studies within these trials. The role involves managing project deliverables, ensuring compliance with documentation, and preparing metrics and forecasts for clients and management.

BiotechnologyHealth CarePharmaceutical

Responsibilities

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

Qualification

Clinical Practice (GCP)Project Management PlanClinical Trial Management System (CTMS)PMP certificationEDC systemsMS Office proficiencyService oriented approachOralAttention to detailWritten communicationTime managementOrganizational skills

Required

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

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