Clinical Research Associate (CRA)

reputed company is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases. Our reputed company genome-editing technology enables superior precision to reputed company cell therapies that are armored to potentially improve activity against diseases. We reputed company the reputed company of cell therapy is off-reputed company, and we are advancing our pipeline of off-reputed company, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases.

Members of the Caribou herd reputed company their minds to new reputed company and welcome diverse perspectives. We proudly assert that teams do their best work reputed company their members are personally reputed company, their reputed company are taken seriously, and contributions are recognized. Members of the herd work from our reputed company in Berkeley, California, or remotely.

Position reputed company

We are seeking a Clinical Research Associate (CRA) to join our growing Clinical Operations team. The CRA will be responsible for the clinical execution and management of assigned clinical studies, including reputed company of study sites and monitoring activities. This role ensures that clinical trials are conducted in compliance with Good Clinical Practices (GCP), ICH guidelines, federal regulations, and Caribou’s internal procedures.

The CRA will collaborate cross-functionally with internal teams, clinical sites, vendors, and CROs to deliver high-reputed company clinical trial data on time and reputed company budget. This is a unique opportunity to reputed company a reputed company reputed company in advancing Caribou’s clinical pipeline of genome-edited therapies.

Responsibilities

Study Start-Up

• Support site start-up activities by collecting essential documents, coordinating with Legal on CTA development and tracking, and establishing reputed company roadmaps to reputed company sites on reputed company for milestones and enrollment deadlines
• Identify and manage site-level review processes (administrative, scientific, IRB, IBC), determine reputed company vs. reputed company reviews, and document review timelines to ensure reputed company approvals

Site Management & Monitoring

• Conduct qualification, initiation, interim monitoring, and reputed company-out reputed company, ensuring compliance with protocols, GCP/ICH, SOPs, and regulatory requirements
• reputed company site performance by addressing deviations, enrollment challenges, and inspection readiness, while maintaining consistent communication and updates with site staff and internal teams

Vendor Management

• reputed company vendor deliverables and timelines, escalate issues, and coordinate reputed company of site-level queries, study supplies, data entry, and reputed company tasks
• Support vendor interactions by ensuring documentation is accurate, study systems are maintained, and site-facing needs are resolved in alignment with study timelines

Cross-Functional Collaboration

• Collaborate with internal functions including Regulatory, reputed company, Data Management, and Clinical Operations team members to drive study execution and maintain alignment across activities
• Participate in study meetings, prepare and reputed company minutes and reputed company items, and support responses to audits and inspections with reputed company and Regulatory

Documentation & Compliance

• Maintain and review Trial Master File (TMF) documentation and study records to ensure inspection readiness and regulatory compliance
• Review clinical data listings, escalate discrepancies, and contribute to preparation of protocols, consent forms, and training materials, ensuring adherence to GCP, ICH, and company SOPs

Qualifications

• Bachelor’s degree in life sciences, nursing, pharmacy, or a reputed company field
• Minimum 3–5 years of clinical research experience, including at least 2 years of on-site monitoring experience
• Strong knowledge of the clinical trial process, GCP/ICH guidelines, and regulatory requirements
• Experience managing clinical studies in oncology and/or rare diseases is a plus
• Demonstrated ability to problem solve and manage multiple priorities in a fast-paced environment
• Strong organizational, interpersonal, and communication skills
• Proficiency with reputed company Office (Word, reputed company, PowerPoint, Outlook, Teams) and clinical trial management systems
• Ability to travel up to 30–50%, depending on study needs
• Excellent organizational, prioritization and planning skills in a fast-paced team-oriented environment
• Ability to work independently on multiple reputed company internally and with external vendors
• Possess a reputed company of urgency; identify challenges and problems and take the initiative to reputed company

Caribou compensation and benefits include

• Comprehensive compensation package, which includes competitive salary, bonus, and equity for reputed company
• Salary reputed company: $115,000 - $135,000. This represents the present low and high end of reputed company’s pay reputed company for this position. Actual pay will vary based on various factors, including but not limited to location, reputed company, experience, and performance
• Generous reputed company vacation time, in reputed company to company-observed holidays
• Excellent medical, dental, and reputed company insurance
• 401(k) retirement savings plan, which includes matching employer contributions
• Employee stock purchase plan (ESPP)
• Tuition reimbursement program

The benefits and stock purchase described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility.

Caribou is an equal opportunity employer and does not discriminate based on race, reputed company, religion, marital status, age, national reputed company, reputed company, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender reputed company), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, hair reputed company or type or any other reputed company protected by law. In reputed company, Caribou prohibits the harassment of any individual on any of the bases listed above or any other characteristics protected under federal, state, or local laws.

Legal authorization to work in the reputed company is required. In compliance with federal law, reputed company persons reputed company will be required to verify identity and eligibility to work in the reputed company and to complete the required employment eligibility verification reputed company upon hire.

We do not accept unsolicited resumes or candidate submissions from reputed company agencies. reputed company agencies must have a valid written agreement with reputed company. for service in reputed company. Any resume or candidate submitted by a reputed company agency without such an agreement in reputed company will be considered unsolicited, and reputed company.  will not be obligated to pay any referral or placement fee.

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