READING CENTER PROJECT MGR.

Duke CareersDurham, NC
3d$23 - $34

About The Position

School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more than 6,000 staff, the Duke University School of Medicine along with the Duke University School of Nursing, Duke University Health System and the Private Diagnostic Clinic (PDC) comprise Duke Health. a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Primary Care, Duke Home and Hospice, Duke Health and Wellness, and multiple affiliations. This position will report to the Administrative Manager and will assist the Project Manager with a variety of duties to support the Duke Reading Center. Position Summary The Project Manager Assistant (PMA) performs a variety of research and administrative duties to support the management of clinical trials at the Duke Reading Center (DRC) for which the DRC serves as the imaging core laboratory. He/she performs a variety of independent duties involved in the collection, documentation, and compilation of clinical research images and data under the direction of the Project Manager. The PMA helps to assign reader grading tasks, file study documents, distribute site initiation forms, track certification of site technicians, and track submission of images and functional tests for grading. He/she also helps to query sites, enter data (DE), perform source document verification (SDV), and conduct quality control (QC) activities such as reconciliation and reconciliation verification (RV). The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Requirements

  • Completion of a Bachelor’s Degree in a related field. At least one year of directly related experience in clinical research is preferred.
  • Excellent oral and written communication
  • Capable of exercising good judgment
  • Ability to be flexible when priorities change
  • Ability to deal with a variety of constituents efficiently
  • Ability to learn new programs quickly
  • Organizational skills
  • Ability to work under deadline pressure
  • Ability to prioritize work assignments
  • Ability to be flexible when work assignments change
  • Enjoys and can effectively multitask
  • Excellent knowledge of Microsoft Excel and Outlook
  • Work requires analytical, communications, and organizational skills generally acquired through completion of a bachelor's degree program.
  • None above education listed above.
  • None above education listed above.

Responsibilities

  • Communicate with sites, sponsors, and CRO’s regarding study specifics and image issues
  • Assist with study startup and site certification activities
  • Track, confirm, and document receipt of all images and functional test materials received at DRC
  • Manage certification reader assignments and assist with all other reader assignments as needed
  • Respond to data queries as appropriate
  • Prepare materials for and perform data QC Review, i.e. reconciliation and reconciliation verification
  • Perform data entry (DE), source document verification (SDV), filing and other clerical duties as requested
  • Assist all DRC staff members as necessary to meet the needs of the various studies
  • Attend DRC group meetings as needed
  • Attend study conference calls, as apropriate
  • Provides coverage for assigned studies when PM is out of the office or unavailable. This may include time sensitive activities such as patient screening eligibilities and sponsor requests
  • help train new PMA’s
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