Senior Clinical Research Associate

United States·South San Franciscosenior

HealthcareClinical Researcher

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Quick Summary

Key Responsibilities

Assist the Clinical Operations team with on-site sample operations, including sample receipt, registration, and shipments in a GCP environment. Support clinical trial manager with site management,

Technical Tools

HealthcareClinical Researcher

Who Are We?

Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.

We are looking for exceptional team members who want an active role in building a rapidly growing biotech.

Position: Senior Clinical Research Associate

Location: South San Francisco, CA

Responsibilities

~1 min read

→Assist the Clinical Operations team with on-site sample operations, including sample receipt, registration, and shipments in a GCP environment.
→Support clinical trial manager with site management, including: site startup activities, co-monitoring visits alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other duties as needed, in alignment with study priorities and CTM guidance.
→Assist clinical trial manager with data verification and ICF reviews as needed, alongside CRO, to support data quality and protocol compliance.
→Partner with CTM and clinical team to help identify areas to improve our processes, with priorities defined by the CTM, and support implementation of agreed-upon improvements.
→Identify and communicate site-level issues, protocol deviations, and operational risks to the CTM to support timely resolution.
→Maintain study trackers, logs, and documentation across regulatory, site, data, and sample operations to support study oversight and execution.

Requirements

~2 min read

Bachelor’s degree in life sciences or related field preferred
2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment)
Strong understanding of GCP, ICH guidelines, and clinical trial processes
Experience working with CROs and managing clinical sites
Excellent organizational, communication, and problem-solving skills
Ability to manage multiple priorities in a fast-paced environment

Compensation: The salary range for this position is $115,000 to $121,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.

Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.

Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.