Job Description
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) (Advantage)
- 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
- 1 year
Schedule :
8 hour shift
Ability to Relocate :
San Antonio, TX : Relocate before starting work (Required)
Work Location : In person
Company Description
Great Clinical Research Company; Looking for great talent.
Company Description
Great Clinical Research Company; Looking for great talent.
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