```Duties:```
- Conduct clinical research activities in accordance with protocols, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Monitor and manage clinical trials to ensure compliance with study protocols, regulatory requirements, and ethical considerations.
- Collect and analyze data from clinical trials, including patient demographics, medical histories, and laboratory results.
- Coordinate with investigators, study coordinators, and other healthcare professionals to ensure smooth execution of clinical trials.
- Perform site visits to assess study progress, ensure data integrity, and provide guidance on protocol adherence.
- Prepare and maintain study documentation, including case report forms (CRFs), informed consent forms (ICFs), and study reports.
- Collaborate with cross-functional teams to support the development and implementation of clinical research projects.
- Stay updated on industry trends, regulatory changes, and best practices in clinical research.

```Requirements:```
- Bachelor's degree in a scientific or healthcare-related field.
- Previous experience in clinical research or a related field is preferred.
- Knowledge of clinical trial processes, regulations, and guidelines (e.g., ICH-GCP).
- Familiarity with statistical software for data analysis (e.g., SAS, SPSS).
- Strong attention to detail and ability to accurately collect and record data.
- Excellent organizational skills to manage multiple tasks and prioritize workload effectively.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently as well as part of a team in a fast-paced environment.
- Strong communication skills to effectively interact with study personnel and stakeholders.

Note: This job description is intended to provide a general overview of the position. Duties and responsibilities may be subject to change based on organizational needs.

Please submit your resume along with a cover letter detailing your relevant experience. Only qualified candidates will be contacted for further consideration.

Job Type: Full-time

Pay: $45.00 - $55.00 per hour

Benefits:

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

Schedule:

• Monday to Friday

Experience:

• Clinical Monitoring: 2 years (Required)

Ability to Relocate:

• Alameda, CA 94501: Relocate before starting work (Required)

Work Location: In person