Role Description
As a Temporary Patient Data Coordinator, youβll support sponsor-facing clinical trial work through accurate, timely data entry and related operational tasks. The day-to-day scope is similar to the full-time version of the role, with a focus on maintaining data quality, following structured processes, and helping the team stay on track during a period of increased trial activity.
-
Enter and maintain clinical trial data accurately and consistently in the systems used for this work.
-
Complete assigned daily tasks while managing your own time and priorities.
-
Review your work carefully to help ensure data quality before submission.
-
Communicate clearly with team members when you have questions, need help prioritizing, or identify an issue.
-
Support routine operational workflows tied to clinical research studies.
-
Follow training, procedures, and guidance to complete work in line with team expectations.
-
Help the team stay on track during a period of increased trial activity.
Qualifications
-
Prior exposure to clinical research, healthcare, patient scheduling, medical assistant work, data entry, or administrative operations.
-
Experience working with structured processes, checklists, task queues, or high-volume detail-oriented work.
-
A background or interest in healthcare, research, data-focused work, or a related field.
Requirements
-
Careful review of your work to catch errors and maintain accuracy.
-
Ability to stay organized and manage a task list independently in a remote setting.
-
Dependability, including showing up on time and following through on assigned work.
-
Clear communication skills and willingness to ask questions when priorities or instructions are unclear.
-
Sound judgment and problem-solving skills when managing competing tasks.
-
Professional work experience, internship experience, or other experience that demonstrates accountability and follow-through.
-
Interest in healthcare, clinical research, data, or a related field.
-
Comfort working in a role where quality matters and mistakes can create downstream issues for the team and sponsors.
Benefits
-
Compensation range: $20 to $22/hr.
-
Limited-term contract role.
-
Expected need is approximately 3β4 months.
-
Multiple hires are planned for this role, with start dates determined during the hiring process.
Company Description
DelRicht Research is an integrated organization of premier investigational sites in the United States. Our mission is to move medicine forward by providing the best quality service to our clients and engaging more volunteers in clinical research.