Clinical Research Coordinator (CRC)

(SALARY WILL BE BASED ON YOUR EXPERIENCE)

Job description

Responsibilities:
- Coordinate and oversee clinical research studies from start to finish
- Collect, analyze, and manage research data in accordance with study protocols and regulatory requirements
- Ensure compliance with HIPAA regulations and maintain patient confidentiality
- Maintain accurate and up-to-date records of study participants and their progress
- Supervise and train research staff on study procedures and protocols
- Monitor patients during clinical trials and record vital signs as necessary
- Perform phlebotomy and collect biological samples for analysis
- Collaborate with investigators, sponsors, and other stakeholders to ensure adherence to clinical trial standards

Qualifications:
- Bachelor's degree in a related field (e.g., biology, healthcare, life sciences)
- Knowledge of medical terminology and clinical research practices
- Experience in data management and analysis
- Familiarity with HIPAA regulations and patient privacy laws
- Strong organizational skills with attention to detail
- Ability to supervise and train research staff effectively
- Proficient in conducting patient monitoring and recording vital signs
- Experience in phlebotomy techniques is preferred but not required
- Understanding of clinical trials management and adherence to industry standards

Note: This job description is intended to provide a general overview of the position. It is not an exhaustive list of responsibilities, qualifications, or benefits associated with the role.

Job Types: Part-time, Contract, Temporary

Benefits:

• Dental Insurance
• Health insurance
• Paid time off
• Vision insurance

Experience level:

• 1 year

Schedule:

• 8 hour shift

Ability to Relocate:

• San Antonio, TX: Relocate before starting work (Required)

Work Location: In person