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Oncology Project Manager @Merit Cro Inc

[Hiring] Oncology Project Manager @Merit Cro Inc

Mar 18, 2025 - Merit Cro Inc is hiring a remote Oncology Project Manager. 💸 Salary: unspecified. 📍Location: USA.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more.

Role Description

MERIT is seeking a Project Manager that accomplishes the day-to-day operations of project management and accurately and competently administers activities regarding assigned studies. Responsible for all study activities; study start up through closeout. Primary functions include assisting project team management of clinical trial data in the EXCELSIOR™ cloud application environment; perform data upload, quality control functions; maintenance of controlled documents including Master Project Files; and provide support functions for clinical sites, reading centers and clients using EXCELSIOR according to MERIT and/or study specific procedures and Good Clinical Practices (GCP).

  • Manage office tasks including organization and coordination of controlled documents
  • Assist in development of project and regulatory documents; includes proofreading of documents
  • Respond to quality review audits and clearly document responses to facilitate resolutions
  • Assist with the development/implementation of training programs
  • Monitor own work to ensure quality and completeness
  • Ability to work with limited supervision
  • Perform and oversee all study activities from start-up through close out and data lock
  • Organize and prioritize work assignments to complete assignments and tasks on time and with quality
  • Prepare study start up materials, organize and conduct internal study start up meeting, and follow up on action items
  • Establish and maintain routine communication among internal MERIT departments, sponsors, site staff, and other designated parties
  • Assist with the development of new study specific processes and procedures
  • Initiation of Master Project File and maintenance of project documents
  • Establish study files and create and distribute study documents
  • Attend project meetings internally and with sponsor (via teleconference or face-to-face) throughout the project
  • Maintain established study specific systems and procedures for regular status updates, site information lists, revisions of plans or study documents and routine correspondence
  • Generate and email eligibility and progression confirmation reports and notifications
  • Generate and provide study reports and updates
  • Independently process clinical data from start up through database lock prioritizing work to meet project timelines
  • Responsible for assisting in all aspects of study conduct, initiation through closeout
  • Understand the EXCELSIOR product, protocol, and conduct of clinical trials in sufficient detail
  • Provide guidance and training to sponsors, CROs, and clinical sites on the use of EXCELSIOR
  • Ensure accurate and efficient set up of EXCELSIOR for assigned project(s)
  • Work closely with the POM group to complete the initial configuration of studies within EXCELSIOR
  • Assist with the review of EXCELSIOR study specific configuration
  • Develop and perform project specific user acceptance testing
  • Ensure the internal team is appropriately trained in the use of EXCELSIOR
  • Manage and review site surveys; update EXCELSIOR for site registration
  • Clinical site technician and equipment certification as needed
  • Image check-in and quality control as needed
  • Issue and review data query responses to ensure completeness and accuracy
  • Review, categorize, and respond to customer support and complaint tickets in the helpdesk application
  • Follow up with sites, sponsors, and reading center personnel on EXCELSIOR access
  • Comply fully with company policies and Standard Operating Procedures (SOPs)

Qualifications

  • Minimum of a Bachelor’s degree in a health related, biological science, computer science, data entry, customer service or business management is preferred
  • A minimum of two (2) years of clinical trial or project management experience in a related field
  • Strong interpersonal and organizational skills
  • Excellent attention to detail
  • Ability to follow direction, assess Company needs and work independently
  • Computer skills to include proficiency in Microsoft Office software and ability to learn Company specific software
  • Ability to participate and contribute in a team environment
  • Oral and written communication is clear, concise, and effective

Requirements

  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

Benefits

  • 401(k)
  • Dental insurance
  • Disability insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance

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📍 Be aware of the location restriction for this remote position: USA
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Oncology Project Manager @Merit Cro Inc
Project Management
Salary 💸 unspecified
Remote Location
USA
Job Type full-time
Posted Mar 18, 2025
Apply for this position Unlock 52,220 Remote Jobs
📍 Be aware of the location restriction for this remote position: USA
Beware of scams! When applying for jobs, you should NEVER have to pay anything. Learn more.
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