Note: The job is a remote job and is open to candidates in USA. DelRicht Research is an integrated organization of investigational clinical research sites focused on advancing medicine through high-quality clinical research services. The EDC Specialist, Limited Term will support clinical trial operations through accurate data entry, data quality review, and routine operational workflows while independently managing assigned tasks in a remote environment.
Responsibilities
- 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
Skills
- 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
- 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
Benefits
- Limited-term contract role
- Expected need is approximately 3–4 months
- You’ll gain practical exposure to clinical trial operations and data quality standards, along with structured training and real responsibility from the start.
- Remote work environment
Company Overview