Clinical Research Coordinator

```Duties```
- Coordinate and oversee Clinical Research studies from start to finish
- Ensure compliance with FDA regulations, study protocols, and ethical guidelines
- Collect, record, and manage data related to the research study
- Perform documentation review and maintain accurate study records
- Monitor patient vital signs and assist with patient monitoring during the study
- Collaborate with investigators, sponsors, and other healthcare professionals involved in the research
- Assist with data collection and analysis using statistical software
- Maintain study supplies and inventory

```Qualifications```
- Bachelor's degree in a related field (e.g., healthcare, life sciences)
- Prior experience working as a Clinical Research Coordinator or in a similar role
- Strong knowledge of Clinical Research processes and regulations
- Proficiency in data management and documentation review
- Familiarity with statistical software for data analysis
- Excellent organizational and time management skills
- Attention to detail and ability to maintain accurate records
- Strong communication and interpersonal skills for effective collaboration with team members

Note: This job description is intended to provide a general overview of the position. Duties, responsibilities, and qualifications may be adjusted or expanded based on the specific needs of the research organization.

Job Type: Full-time

Pay: $28.00 - $32.00 per hour

Expected hours: 40 per week

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Experience level:

• 1 year
• 2 years

Medical specialties:

• Oncology

Schedule:

• 8 hour shift
• Monday to Friday

Ability to Relocate:

• Dallas, TX: Relocate before starting work (Required)

Work Location: In person