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.

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