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Clinical Research Coordinator II - Psychiatry CNY

Davita Inc.

Boston (MA)

On-site

USD 50,000 - 70,000

Full time

Yesterday
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Job summary

Davita Inc. is seeking a full-time Research Coordinator for its Geriatric Psychiatry Program. The role involves overseeing clinical trials, data management, recruitment, and supporting publications related to NIH-funded mental health studies. Ideal candidates will have strong organizational and analytical skills to contribute throughout all phases of research.

Qualifications

  • Experience in research coordination preferred.
  • Ability to manage data and reports effectively.
  • Strong communication and organizational skills.

Responsibilities

  • Oversee activities for clinical trials and pilot projects.
  • Collect and organize patient data for research.
  • Assist with regulatory submissions and compliance.

Skills

Data management
Patient recruitment
Analytical skills
Communication
Literature search

Tools

Statistical software

Job description

The Department of Psychiatry is seeking a Research Coordinator to work with a group in the Geriatric Psychiatry Program on NIH-funded grants related to mental health and mild cognitive disorders. The position is full-time, 40 hours/week, reporting to the Principal Investigator. The coordinator will oversee activities for clinical trials and pilot projects, including recruitment, IRB applications, study coordination, communication with participants, data management, and support for publications and grant reporting.

The Research Coordinator may participate in all project phases, from conception to analysis and manuscript preparation.

Major duties:
  • Coordinate research activities and assist with regulatory submissions
  • Collect and organize patient data
  • Maintain records and databases
  • Use software to generate reports and graphs
  • Assist with patient recruitment and screening
  • Conduct literature searches
  • Verify and update study forms
  • Document patient visits and procedures
  • Assist with interviewing and consenting study subjects
  • Administer and score questionnaires
  • Perform study procedures and assist with regulatory compliance
  • Contribute to data analysis, report writing, and presentation of results

The University is an Equal Opportunity Employer. We value diversity and encourage all qualified applicants to apply. We provide reasonable accommodations for individuals with disabilities throughout the hiring process and employment.

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