Clinical Research Coordinator (CRC)

Job Description

(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 personCompany Description

Great Clinical Research Company; Looking for great talent.