Job Description
Clinical Research Associate
6-month contract - highly likely to extend
Onsite in Alameda 5 days per week
Key Responsibilities:
- Proactively identify and address issues related to study monitoring and site management.
- Track and communicate monitoring updates and site performance; escalate risks to clinical leadership as needed.
- Support internal processes such as onboarding, protocol training, and maintenance of monitoring tools and study documentation templates.
- Manage and oversee CROs and vendors involved in study operations, including monitoring, site management, data management, and project master file maintenance.
- Ensure compliance with GCP, industry standards, SOPs, and regulatory requirements across all assigned study activities.
- Operate independently with minimal supervision, managing multiple priorities in a dynamic environment.
- Contribute to departmental initiatives and take on additional projects as assigned.
Qualifications:
- Bachelor’s degree in Biology, Health Sciences, Mathematics, Computer Science, or a related field.
- Prior experience in clinical research or clinical trials is required.
- Solid understanding of clinical trial processes, monitoring practices, and regulatory requirements.
- Strong organizational, problem-solving, and communication skills.
- Ability to work independently and collaboratively in a cross-functional team setting.
Job Tags
Contract work,