Top 69 Clinical trial manager Jobs in Brisbane Ca

Clinical Trial Manager
CareDx, Inc. —Brisbane, CA
- $124,000 - $155,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
- Commuter assistance
- Employee stock purchase plan
Clinical Trial Manager/Sr Clinical Trial Manager
Erasca —South San Francisco, CA
- $145,000 - $190,000 a year
- Remote
- Medicine
- Inventory management
- 5 years
- Health savings account
- AD&D insurance
Senior Clinical Trial Manager
Nura Bio —South San Francisco, CA
- 7 years
- Bachelor of Science
- Presentation skills
- Disability insurance
- Health insurance
Quick Apply
Clinical Trial Manager
Evommune, Inc. —Palo Alto, CA
- $120,000 - $150,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Paid parental leave
- Disability insurance
Quick Apply
Clinical Research Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Nursing
- RN License
- BLS Certification
Clinical Trial Manager (Office Based - South SF 3X/wk)
Zai Lab (US) LLC —South San Francisco, CA
- $145,000 - $170,000 a year
- Full-time
- Hybrid work
- Office
- Quality control
- Travel
- Paid time off
- Parental leave
Quick Apply
8h
Clinical Supply Manager
Vera Therapeutics, Inc. —Brisbane, CA
- $110,000 - $135,000 a year
- Master's degree
- Bachelor's degree
- Business Administration
- Paid holidays
- Health insurance
Manager, Clinical Research
CUTERA INC —Brisbane, CA
- $140,000 - $160,000 a year
- Full-time
- Microsoft Excel
- Management
- 5 years
Quick Apply
Clinical QC Manager- Hybrid
Zai Lab (US) LLC —South San Francisco, CA
- $145,000 - $170,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Parental leave
Quick Apply
Clinical Research Supervisor
University of California San Francisco —San Francisco, CA
- Contract
- Word processing
- HIPAA
- Ob/Gyn
Research Program Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Medicine
- Surgery
- Research
Study Project Manager II - Hybrid
AbbVie —South San Francisco, CA
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- 8 years
- Bachelor's degree
- Mentoring
- Paid holidays
- Health insurance
2d
Manager, Clinical Operations
iota Biosciences, Inc. —Alameda, CA
- $145,000 - $200,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Mentoring
- Senior level
- Paid parental leave
- Health insurance
1d
Senior Clinical Trials Manager
Zai Lab (US) LLC —South San Francisco, CA
- $177,000 - $229,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Parental leave
Quick Apply
8h
Senior Global Clinical Study Manager
IQVIA —San Francisco, CA
- $93,100 - $232,800 a year
- Full-time
- Customer service
- Bachelor's degree
- Continuous improvement
14d
Clinical Research Manager - Heme Malignancy Program
University of California San Francisco —San Francisco, CA
- Customer service
- Word processing
- 3 years
Protocol Project Manager
University of California San Francisco —San Francisco, CA
- Microsoft Excel
- Bachelor of Science
- Organizational skills
Clinical Trials Manager (Biotechnology, Oncology)
Exelixis, Inc. —Alameda, CA
- $136,000 - $192,500 a year
- Full-time
- Bachelor's degree
- Continuous improvement
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Clinical Trials Manager
Gilead Sciences —Foster City, CA
- $146,540 - $189,640 a year
- Full-time
- Bachelor of Science
- Office
- 3 years
- Health insurance
- Dental insurance
Sr. Project Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Laboratory experience
- 8 years
- University

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Clinical Trial Manager

CareDx, Inc. -
Brisbane, CA

Apply Now

Job Details

Full-time
$124,000 - $155,000 a year

Benefits

Commuter assistance
Employee stock purchase plan
Health insurance
401(k) matching
Gym membership

Qualifications

Biotechnology
ICH guidelines
Project management experience in healthcare
Medical laboratory work experience
Managing projects
Clinical quality assurance standards
Medical terminology
FDA regulations

Full Job Description

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.

This position provides direction and operational leadership of the clinical research studies to ensure delivery on time. The Clinical Trial Manager (CTM) is responsible for the management of clinical trials from study start-up activities through the clinical study report. The CTM drives completion of all study deliverables, ensuring the highest level of data quality and compliance to quality standards and regulatory guidance; proactively identifies, communicates and resolves clinical study operational issues; and participates in process improvement initiatives as required.

Specific responsibilities include, but are not limited to:

Lead the end-to-end execution of CareDx clinical trials, including but limited to site identification, study start-up, study conduct, monitoring and closeout, with full accountability of study timelines, budget and metrics; study submission to IRB/ECs; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab test requisitions, etc.), plans and managing study-specific meetings (e.g. Study Team Meetings, Investigator meetings, etc.)
Drive site activation, enrollment, and overall study performance while ensuring alignment with protocols, operational plans, and business objectives.
Proactively identify study risks (timeline, quality, and operational), lead mitigation planning and execution, and escalate issues effectively with clear action plans, defined ownership, and accountability
Conduct internal review of investigator contracts and payments, as necessary.
Provide cross-functional leadership across Clinical Operations, Data Management, Medical Affairs and other functional areas serving as the central point of coordination to ensure clear roles, accountability, and seamless clinical trial execution.
Prepare and present project debriefings to Clinical Operations management and cross-functional teams.
Oversee Clinical Research Associates, CROs, central labs, and external vendors to ensure high-quality, timely, and cost-effective deliverables through established governance, KPIs, and performance management processes.
Champion operational excellence by standardizing study execution models, optimizing vendor management and reporting frameworks, and implementing scalable process improvements and SOPs.
Ensure data quality and inspection readiness through proactive data review, performance metric tracking, and close collaboration with monitoring and data management teams. Identify and mitigate risks across timelines, quality, and operations, driving effective escalation and resolution strategies.
Maintain strong communication with clinical sites and stakeholders, including oversight of site visits, study documentation, and reporting, while ensuring compliance with GCPs, regulatory requirements, and study protocols.
Support study administration activities such as site engagement, training, and product inventory management to ensure efficient and compliant study execution.
Ensure high-quality, inspection-ready documentation and study tracking through effective use of eTMF including oversight of TMF completeness, document quality, and real-time study status reporting
Provide oversight and operational support for CTMS system and effective use of it for tracking study milestones, enrollment, monitoring activities, and performance metrics

Minimum Qualifications

Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or pharmaceutical experience preferred but not required
Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry
Robust understanding of ICH/GCP, and knowledge of regulatory requirements.
Working knowledge of medical terminology.
Experience with medical laboratory testing and documentation of patient information.
Comfortable with technology and scientific/engineering principles.

Skills and Experience:

A critical thinker and capable of problem solving and aligning the priorities with study outcomes and timelines.
Strong clinical study/project management skills.
Excellent communication, written and organizational skills (ability to prioritize a number of tasks of varying complexity), along with problem solving, conflict resolution, leadership and team-building skills.
Ability to motivate and collaborated with teams at other functional departments.
Ability to work independently, take initiative, and meet company goals within timelines and budget.
Able to work in a fast-paced environment with multiple competing tasks and demands, across time-zones.
Must have a sense of urgency about problem-solving and completing projects.
Ability to communicate with vendors and keep a high quality of clinical study
Strong knowledge of FDA regulations and GCP.
Proficient in Microsoft Office (excel, word, outlook, power point), electronic data capture (EDC) software (Medrio, Medidata) and other platform related to electronic Trial Master File (eTMF), CTMS and safety report

SCOPE OF WORK

Travel estimate 10-30% .
Operate within standard guidelines, but must engage in some independent decision-making.
Errors that are not quickly detected and rectified could have a significantly adverse effect on the quality of the study.
Works closely with other Clinical Research staff, as well as staff from other departments.

PREFERENCES

Experience with clinical studies involving organ transplantation.

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 https://caredx.com/company/careers

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-vets/disabled, 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 Notice and consent to receive email communication from CareDx. Certain jurisdictions require notice of how we use and protect your personal information. For more information, please read our Privacy Policy

The U.S. EEO posters are available here.

Note: We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us.

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Refine Your Search

clinical trial manager jobs in brisbane ca

Clinical Trial Manager

Clinical Trial Manager/Sr Clinical Trial Manager

Senior Clinical Trial Manager

Clinical Trial Manager

Clinical Research Manager

Clinical Trial Manager (Office Based - South SF 3X/wk)

Clinical Supply Manager

Manager, Clinical Research

Clinical QC Manager- Hybrid

Clinical Research Supervisor

Research Program Manager

Study Project Manager II - Hybrid

Manager, Clinical Operations

Senior Clinical Trials Manager

Senior Global Clinical Study Manager

Clinical Research Manager - Heme Malignancy Program

Protocol Project Manager

Clinical Trials Manager (Biotechnology, Oncology)

Clinical Trials Manager

Sr. Project Manager

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