Jobs · Analyst · Missouri

Clinical Research Coordinator

EyeCare Partners · Des Peres, MO · 1 wk ago
On-siteAnalystFull-time

Duties

  • Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.
  • Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues. Follow GCP guidelines. Implement confidentiality and privacy regulations.
  • Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and prepare study budgets.
  • Support and assist Research personnel in the operation of equipment used in clinical trials.
  • Auxiliary in the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers.
  • Auxiliary in the preparation of annual IRB reviews.
  • Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
  • Understand the operational budget and sub-contracts; track documentation and authorization of payment of study related bills.
  • Prepare project reports for PI review and approval.
  • Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments with study participants.
  • Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements for complex study protocols, and perform technical duties as assigned.
  • Support orientation and structured intervention sessions in accordance with technical training and certification(s).
  • Assist with case management activities to support the work of the project(s).
  • Support the process of summarizing and sharing project information with other sites.
  • Support the Project Director, Clinic Coordinator, and/or PI in the maintaining regular contact with other Project Administrators in order to share information and ideas.
  • Auxiliary in the tracking of papers in process for projects, with planning for project papers and posters to be presented at national and international conferences.

Qualifications

  • Demonstrated interpersonal, communication and interviewing skills with people of all ages.
  • Organized, detail oriented, self-directed and dependable.
  • Able to prioritize work, solve problems and work independently.
  • Able to function in a team environment and use negotiation skills.
  • Favorable result on background check required.
  • Must be able to provide proof of identity and right to work in the United States.

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