Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Sr. Clinical Research Associate

Job

Bayside Solutions

Remote

$166,400 Salary, Full-Time

Posted 4 weeks ago (Updated 2 days ago) • Actively hiring

Expires 7/26/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
76
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Sr. Clinical Research Associate in Redwood City, California Overview Sr. Clinical Research Associate W2
Contract Pay Rate:
$75 - $85 per hour
Location:
Redwood City, CA -
Hybrid Role Job Summary:
Sr. Clinical Research Associate (Sr. CRA) will provide appropriate sponsor oversight of sites and conduct clinical research activities according to SOPs and applicable regulations and guidelines. The Sr. CRA will work in a fast-paced environment and proactively communicate with investigators, colleagues, and vendors to ensure clinical quality and compliance in the conduct of clinical trials.
Duties and Responsibilities:
Support activities within various phases of clinical studies (i.e., study planning, site qualification, and investigator selection, monitoring, closeout, etc.) Support the study team through the development of clinical study plans, presentations, study documents (review and approval of informed consent forms (ICFs), site-facing documents, and tracking tools, review and tracking of monitoring reports, sample tracking, and other activities as needed. Attend monitoring visits with CRO CRAs to develop site relationships and ensure training and oversight of the CRO. Drive site performance and engagement through regular communications and by setting clear expectations, providing feedback, and developing action plans for remediation when needed Build and maintain strong relationships with investigators and staff. Assure compliance with local regulations, Code of Federal Regulations (CFR) / International Conference of Harmonization (ICH) and GCP guidelines, and
Company and SOPs Requirements and Qualifications:
Degree in sciences/health care field, nursing degree, or equivalent, combined with education and experience 3+ years' experience as a Clinical Research Associate (CRA) from biotech or pharma required Certificate in Clinical Research or Certified Clinical Research Associate (CCRA) credentials preferred Domestic and international travel up to 10%, possibly Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s