Cogstate
Cogstate
Cogstate develops digital tools for measuring cognition and brain health, with a focus on clinical research and trials. Its assessment and screening solutions support remote testing and endpoint data quality in studies of conditions including Alzheimer’s disease, Parkinson’s disease, and multiple sclerosis. Founded in 1999, Cogstate works with biopharmaceutical companies, academic institutions, and healthcare providers to provide cognitive measurement for research.

Clinical Trial Associate, Rater Services

Support Cogstate’s digital cognitive assessment studies by coordinating rater training and clinical trial operations. Manage site relationships, study reporting, and delivery of project milestones.

Apraksts

  • Coordinate work across teams to deliver Cogstate’s Rater Training Program on schedule.
  • Connect Scale Management, the Clinician Network, Science, Site Training and Monitoring, and sponsor-appointed training contacts.
  • Manage study reports and working relationships with sites, raters, clinical research associates, and sponsors.
  • Oversee quality management for assigned clinical trial programs.
  • Keep records accurate, update trackers promptly, and handle high volumes of email and site communications.
  • Adapt assignments as studies change and priorities shift.
  • Mentor junior study team members and review their work.
  • Assist Rater Services Managers with limited supervision.
  • Serve as the main contact for sites, raters, and CROs from study start-up through close-out.
  • Coordinate project work to deliver client commitments on time.
  • Provide operational support to site staff throughout each study.
  • Manage Phase I–III trials in line with each project’s statement of work.
  • Monitor key milestones and share updates with the study project manager, sponsor, or Rater Training Lead.
  • Lead rater training for small and medium-sized studies when assigned.
  • Arrange communications and schedules for consultant LEADs.

Prasības

  • Bachelor’s degree or at least three years of relevant experience.
  • At least two years of clinical trial-related work experience.
  • Study start-up experience is an advantage.
  • Experience as a CRA or in a CRO is an advantage.
  • Project management or service industry experience is preferred.
  • Able to manage several tasks while staying organized, methodical, and attentive to detail.
  • Strong interpersonal skills with colleagues, customers, and external providers.
  • Learns quickly and can work independently, plan ahead, and take initiative.
  • Confident with computers; clinical software experience is preferred.
  • Able to work effectively in a fast-moving, expanding environment.
  • Strong written and verbal communication skills.
  • Able to resolve conflicts.
  • Proficient with Excel and Microsoft Office.
  • Maintains precise records and follows procedures.
  • Able to manage competing tasks and priorities.

Priekšrocības

  • Performance-based bonus with a target of 5% of annual base pay.
  • Remote work from anywhere in the United States.
  • 20 days of vacation leave.
  • 10 days of personal leave.
  • 10 paid public holidays.
  • 401(k) matching up to 3% of annual pay.
  • Competitive base pay with additional earning opportunities.
  • Health and dental insurance with competitive employer contributions.
  • Free vision insurance for full-time employees.
  • Short-term and long-term disability and life insurance fully paid by the employer.
  • Healthcare and Dependent Care Flexible Spending Accounts.
  • Learning and development support, including mentorship and help with training programs or certifications.

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