Top 98 Clinical trial manager Jobs in Burlingame, Ca

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
Clinical Trial Manager
Sagimet Biosciences —San Mateo, CA
- $90 - $100 an hour
- Hybrid work
- Nursing
- 3 years
- Analysis skills
Clinical Trial Manager, CKD
Maze Therapeutics —South San Francisco, CA
- $143,000 - $175,000 a year
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Manager (Retina)
4D Molecular Therapeutics —Emeryville, CA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- 6 years
- Microsoft Outlook
Clinical Trial Manager
CareDx, Inc. —Brisbane, CA
- $124,000 - $155,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Inventory management
- Commuter assistance
- Employee stock purchase plan
Sr. Clinical Trial Manager
Synthekine —Menlo Park, CA
- $175,000 - $189,000 a year
- Customer service
- Bachelor of Science
- HIPAA
- Commuter assistance
- Health savings account
14d
Clinical Research Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Nursing
- RN License
- BLS Certification
Clinical Trial Manager (CTM)
Corcept Therapeutics —Redwood City, CA
- $156,600 - $184,300 a year
- Hybrid work
- Nursing
- 6 years
- Bachelor of Science
Quick Apply
SR. CLINICAL TRIAL MANAGER
Sutro Biopharma —South San Francisco, CA
- $155,000 - $175,000 a year
- Full-time
- Nursing
- Microsoft Outlook
- LVN
Clinical Trials Manager, Early Phase Oncology (Office Based)
Gilead Sciences —Foster City, CA
- $133,195 - $189,640 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Health insurance
- Dental insurance
Senior Clinical Trial Manager
Nura Bio —South San Francisco, CA
- 7 years
- Bachelor of Science
- Presentation skills
- Disability insurance
- Health insurance
Quick Apply
Study Project Manager I - Hybrid
AbbVie —South San Francisco, CA
- $109,500 - $208,500 a year
- Full-time
- Hybrid work
- 6 years
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid holidays
- Health insurance
6d
Clinical Trial Manager
Intuitive Surgical —Sunnyvale, CA
- $128,900 - $218,300 a year
- Day shift
- Surgery
- 3 years
- Bachelor's degree
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
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
Senior Clinical Trial Manager (Sr CTM)
Corcept Therapeutics —Redwood City, CA
- $170,500 - $200,700 a year
- Hybrid work
- Nursing
- Bachelor of Science
- Office
Quick Apply
Cell and Gene Therapy Discovery Stage Project Manager
Stanford University —Stanford, CA
- $120,038 - $153,486 a year
- Full-time
- Hybrid work
- 5 years
- Office
- University
Clinical Research Manager
Stanford University —Stanford, CA
- $124,521 - $153,615 a year
- Extended hours
- Hybrid work
- 5 years
- HIPAA
- Master's degree
Senior Clinical Study Manager
Intuitive Surgical —Sunnyvale, CA
- $128,900 - $218,300 a year
- Day shift
- Remote
- Surgery
- 5 years
- Bachelor's degree
7d
Manager, Clinical Operations
iota Biosciences, Inc. —Alameda, CA
- $145,000 - $200,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Mentoring
- Paid parental leave
- Health insurance

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Clinical Trial Manager/Sr Clinical Trial Manager

Erasca -
South San Francisco, CA

Apply Now

Job Details

$145,000 - $190,000 a year

Benefits

Stock options
Health savings account
AD&D insurance
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
Pet insurance

Qualifications

Team leadership
Pharmaceutical regulatory compliance
ICH guidelines
Pharmaceutical company experience
Clinical program monitoring
Managing clinical research teams
Vendor relationship management
Managing projects
Clinical team leadership
Clinical quality assurance standards
Oncology
Research and development project management
Pharmaceutical research experience
Project stakeholder communication
FDA regulations

Full Job Description

Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer's most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name "Erasca" has an important embedded meaning: it is a contraction of our audacious hope to "erase cancer" that drives our mission and everything that we do on behalf of patients with cancer.

The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation, and management of clinical studies from concept to completion. The position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines.

Essential Duties and Responsibilities:

Manage global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements.
Recruit global study sites and foster relationships with study investigators.
Participate in the process of site and vendor selection, qualification, and activation.
Develop Requests-for-Proposals and assist in vendor selection efforts.
Assist in review and negotiation of vendor contracts and study site clinical trial agreements.
Manage study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging).
Monitor the progress of trials, including enrollment and clinical trial material inventory.
Review monitoring visit reports for completeness and adherence to the annotations.
Assist in packaging/labeling/distribution of clinical trial material.
Monitor and track biological samples for applicable analyses.
Provide progress updates to management and during program team meetings.
Assist in departmental budgeting, including accruals and projections.
Assist in development of protocols, consent forms, IRB/EC materials, and other trial documents.
Assist in development of Clinical SOPs.
Prepare/review/approve study materials such as CRFs, patient diaries, drug accountability forms, study and investigator manuals, project plans, and monitoring reports.
Assist in electronic case report form design and development.
Assist in IRT design and development.
Participate in data cleaning activities and developing appropriate data outputs.
Understand and help fulfill the needs of other Erasca departments (e.g., Finance, Research).
Provide leadership and mentoring of other Clinical team members.
Perform all duties in keeping with the Company's core values, policies and all applicable regulations.

Required Education, Experience and Attributes:

Preferred undergraduate degree in life sciences or professions (pharmacy, medicine, nursing, or other allied health sciences).
For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations in pharmaceutical company or CRO including trial set-up, monitoring, and close-out of US and non-US trials at all phases of pre-NDA clinical research (Phases 1-3). For Senior Clinical Trial Manager, at least 7 years of relevant experience required.
Demonstrated excellence in trial management skills, with track record of successfully managing multiple projects, trials, and priorities.
Experience with managing study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging).
Ability to work well with global, multi-disciplinary teams.
Experience in practical knowledge and implementation of ICH-GCP guidelines and US and ex-US regulations.
Experience with electronic data capture and data management software.
Experience in the management of Clinical Research Associates.
Excellent oral and written communication skills.
Experience with reviewing monitoring trip reports
Must be able to thrive in an entrepreneurial, fast-paced, and dynamic work environment.
Must be organized and be able to communicate effectively.
Must be a self-starter.
Strong learning orientation, curiosity, and commitment to science and patients.

The anticipated salary range for this position is $145,000 to $190,000. 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, type and length of experience within the industry, education, etcetera. In addition to base salary, the hired applicant will be eligible to receive an annual bonus and an equity grant at hire and annually in the form of the option to purchase stock in the future for a specified price.

Along with our casual, collaborative, and fun work and the chance to make your mark in our mission to erase cancer, Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off, Holiday, and Sick Leave, Medical, Dental and Vision Plans, Short- and Long-Term Disability, Basic and Voluntary Life/AD&D Coverage, Flexible Spending Accounts (FSA, HSA, and Commute), Critical Illness and Accident Coverage, Pet Insurance, Employee Assistance Program, 401(k) Plan with Erasca contribution, and the opportunity to participate in an Employee Stock Purchase Program.

Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.

Apply Now

Refine Your Search

clinical trial manager jobs in burlingame, ca

Clinical Trial Manager/Sr Clinical Trial Manager

Clinical Trial Manager

Clinical Trial Manager, CKD

Clinical Trial Manager (Retina)

Clinical Trial Manager

Sr. Clinical Trial Manager

Clinical Research Manager

Clinical Trial Manager (CTM)

SR. CLINICAL TRIAL MANAGER

Clinical Trials Manager, Early Phase Oncology (Office Based)

Senior Clinical Trial Manager

Study Project Manager I - Hybrid

Clinical Trial Manager

Senior Clinical Trials Manager

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

Senior Clinical Trial Manager (Sr CTM)

Cell and Gene Therapy Discovery Stage Project Manager

Clinical Research Manager

Senior Clinical Study Manager

Manager, Clinical Operations

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