- Work from
- United States
- Contract
- Full-time
- Experience
- Senior
- Salary
- $100K – $130K / year
- Posted
- 11 November 2026
- Apply by
- 10 January 2027
We are seeking a highly skilled and motivated Senior Clinical Research Associate to join our Clinical Operations team. This role is pivotal in ensuring the integrity, quality, and compliance of our clinical trials.
The ideal candidate will bring deep expertise in clinical study management, a passion for improving patient outcomes, and the ability to lead and mentor within a fast-paced, collaborative environment.
Responsibilities
- Conduct and oversee all types of site visits (e.g., selection, initiation, interim, close-out) to ensure protocol adherence, patient safety, and data accuracy.
- Collaborate with Principal Investigators, study coordinators, and cross-functional teams to drive study success.
- Ensure compliance with ICH/GCP, IRB requirements, and internal monitoring plans.
- Identify and resolve data collection issues within electronic data capture (EDC) systems.
- Review and reconcile data queries, listings, and discrepancies.
- Maintain accurate and complete study documentation and files.
- Lead study team meetings and contribute to protocol development and amendments.
- Support site recruitment and provide oversight to ensure enrollment goals are met.
- Mentor junior CRAs and provide technical expertise in clinical programming and data validation.
- Assist in the development and refinement of SOPs, workflows, and templates.
- Partner with Clinical Trials Manager to manage timelines, budgets, and resources.
- Liaise with regulatory authorities and CROs as needed.
- Ensure timely and compliant execution of monitoring reports, trip reports, and follow-up letters.
- Monitor site performance metrics and facilitate effective communication across stakeholders.
Requirements
Qualifications
- Education: Bachelor’s degree or higher in biomedical sciences or a related field.
- Experience: 5+ years of experience in clinical research within biotech, pharma, medical device, or academia.
- Strong knowledge of GCP, FDA regulations, and ISO standards.
- Proficiency in EDC systems, CTMS, and Microsoft Office Suite.
- Certification (CCRC or CCRA) is a plus.
- Excellent understanding of medical terminology and clinical trial processes.
- Proven ability to manage multiple studies and priorities with precision and urgency.
- Exceptional communication, organizational, and interpersonal skills.
- Demonstrated ability to work independently and collaboratively in remote, cross-functional teams.
- Ability to travel up to 75% of the time.
What You Bring
- A proactive mindset and high standards for quality and accuracy.
- Strong analytical and problem-solving skills.
- Ability to adapt quickly to changing demands and environments.
- A customer-focused approach in working with sites and external partners.
- A commitment to continuous improvement and operational excellence.
About CareDx, Inc.
CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients.
Additional Details
Every individual at CareDx has a direct impact on our collective mission to improve the lives of organ transplant patients worldwide. We believe in taking great care of our people, so they take even greater care of our patients.
Our competitive Total Rewards package for US Employees includes:
- Competitive base salary and incentive compensation
- Health and welfare benefits, including a gym reimbursement program
- 401(k) savings plan match
- Employee Stock Purchase Plan
- Pre-tax commuter benefits
- And more!
- Please refer to our page to view detailed benefits at
In addition, we have a Living Donor Employee Recovery Policy that allows up to 30 days of paid leave annually to a full-time employee who makes the selfless act of donating an organ or bone marrow.
With products that are making a difference in the lives of transplant patients today and a promising pipeline for the future, it’s an exciting time to be part of the CareDx team. Join us in partnering with transplant patients to transform our future together.
CareDx, Inc. is an Equal Opportunity Employer and participates in the E-Verify program.
By proceeding with our application and submitting your information, you acknowledge that you have read our U.S. Personnel Privacy Noticeand consent to receive email communication from CareDx.
We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us.
Certain jurisdictions require notice of how we use and protect your personal information. For more information, please read our Privacy Policy.
This is the anticipated base salary range in the United States. The final salary offered to a successful candidate will be dependent on several factors that may include, but are not limited to, the type and length of experience within the job, the type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives and restricted stock units. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states.
Remote: US only roles
$100,000—$130,000 USD
P
C
J
G
Discussion
No comments yet. Ask a question or share a tip about this role.