Top 78 Clinical trial manager Jobs in Oakland Ca

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
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
Neurocentria —Walnut Creek, CA
- $160,000 - $190,000 a year
- Full-time
- Hybrid work
- Nursing
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Quick Apply
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 (CTM)
Corcept Therapeutics —Redwood City, CA
- $156,600 - $184,300 a year
- Hybrid work
- Nursing
- 6 years
- Bachelor of Science
Quick Apply
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
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
SR. CLINICAL TRIAL MANAGER
Sutro Biopharma —South San Francisco, CA
- $155,000 - $175,000 a year
- Full-time
- Nursing
- Microsoft Outlook
- LVN
12d
Manager, Clinical Data Management
Alimentiv —San Francisco, CA
- $99,500 - $160,000 a year
- Full-time
- Remote
- 7 years
- Mentoring
- Recruiting
- Health insurance
- Dental insurance
Quick Apply
9d
Clinical Trial Manager
Sagimet Biosciences —San Mateo, CA
- $90 - $135 an hour
- Hybrid work
- Nursing
- 3 years
- Analysis skills
12d
Senior Clinical Trial Manager
Nura Bio —South San Francisco, CA
- 7 years
- Bachelor of Science
- Presentation skills
- Disability insurance
- Health insurance
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
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
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA —San Francisco, CA
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
13d
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
Senior Global Clinical Study Manager
IQVIA —San Francisco, CA
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
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
11d
Associate Director/Senior Clinical Trials Manager
Riboscience —San Francisco Bay Area, CA
- Email
- Writing skills
- Bachelor's degree
- Continuous improvement
- Paid parental leave
- Disability insurance
Clinical Trials Manager
Riboscience —San Francisco Bay Area, CA
- Email
- Microsoft Office
- 3 years
- Continuous improvement
- Paid parental leave
- Disability insurance

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Clinical Trial Manager (Retina)

4D Molecular Therapeutics -
Emeryville, CA

Apply Now

Job Details

$150,000 - $170,000 a year

Qualifications

Biotechnology

Full Job Description

Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.

4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery

GENERAL SUMMARY:
The Clinical Trial Manager will support the Company's clinical trial activities. This position reports to the Director of Clinical Operations. This will be responsible for management of the day to day operations of one or more phase 1-3 clinical trials including trial start up, conduct and close out activities.

MAJOR DUTIES & RESPONSIBILITIES:

Trial Management:

Serve as the primary contact for managing protocol execution, including oversight of the CRO, other study service providers, and consultants that are involved in a clinical trial
Lead cross-functional study execution team in support of study deliverables
Support establishment of study milestones and ensure accurate tracking and reporting of study metrics and timelines to leadership
Ensure clinical trials are managed and executed in accordance with ICH GCP, regulations, the protocol, and company-specific SOPs
Assist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms, Statistical Analysis Plan, Clinical Study Reports, and other study level documents
Ensure that the Trial Master File (TMF) is set up and maintained appropriately throughout the trial, including periodic reviews
Participate and coordinate resolution of audit finding and ensures audit-ready condition of clinical trial documentation including central clinical files
Participates in service provider selection process as a part of outsourcing activities
Proactively identifies, with the support and guidance from Senior Clinical Operations staff, and supports development of plans and resolution of project issues and participates in process improvement initiatives as required
Supports assessing operational feasibility, recommending study execution plan and site selection under the Director of Clinical Operations
Responsible for the selection and study specific training of CRO study staff, monitors, investigational sites, and service providers
In conjunction with legal group, facilitate the development of clinical trial agreements and other relevant documents
Manage clinical trial budgets, providing ongoing financial reporting and projections
Negotiate and finalize site contracts and budgets
Perform and manage data review process on an ongoing basis
Perform site visits including site qualification, initiation, monitoring and close-out visits, as needed
Oversee outsourced monitoring by reviewing, monitoring reports to ensure quality and resolution of site-related issues
Ensures tracking and review of protocol deviations and assesses impact on study data
Develops and manages study budget and maintain within financial goals; Reviews and approves clinical invoices against approved budget
Provides oversight for forecasting of clinical supplies, including study drug and supplies

Department Management:

May manage and/or oversee work of junior Clinical Operations staff
May support development and review of Clinical SOPs and other department initiatives
Travel as needed to sites, conferences, industry meetings
Other duties as may be assigned

QUALIFICATIONS:

Education:

B.A./B.S. degree in Science

Experience:

6+ years of clinical research experience within the Biotech or similar industry, with at least 2 years directly supporting a retina clinical trial
Global APAC experience desired

Other Qualifications/Skills:

(non-technical and technical skills)

Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management; Strong clinical study management skills
Understanding of, and experience with, regulatory framework applicable to interactions with HCPs, payers, advocacy and other business partners
Proven clinical operational skills to direct protocol execution to ensure timeline, budget and quality metrics are met
Excellent communication skills to effectively disseminate information to project team and outside parties
Experience reviewing trial plans including developing creative strategies for site monitoring, risk mitigation, trial budgets, site selection, and clinical supplies management
Clinical research knowledge and cross-functional understanding of clinical trial methodology
Excellent organizational, conflict resolution, prioritization and negotiation skills
Proven ability in creative problem-solving and exercising sound judgment
Team oriented and ability to effectively collaborate with study team, cross-functional team members, and external partners
Ability to handle a high volume of highly complex tasks within a given timeline
Ability to develop Therapeutic Areas knowledge and expertise through internal training and external conference attendance
Proficient computer skills, specifically with Microsoft Office Suite that include Word, Excel, PowerPoint, and Outlook
Working knowledge of MS Project for development and update of clinical study timelines

Travel: 5%

Physical Requirements and Working Conditions:

Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.
Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally, and all other sedentary criteria are met.
Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).

Base salary compensation range: $150,000 - 170,000

Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate's geographical location, relevant work experience, skills, and years of experience.

4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Apply Now

Refine Your Search

clinical trial manager jobs in oakland ca

Clinical Trial Manager (Retina)

Clinical Trial Manager

Clinical Trial Manager/Sr Clinical Trial Manager

Senior Clinical Trial Manager

Clinical Trial Manager, CKD

Clinical Trial Manager (CTM)

Clinical Trials Manager, Early Phase Oncology (Office Based)

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

SR. CLINICAL TRIAL MANAGER

Manager, Clinical Data Management

Clinical Trial Manager

Senior Clinical Trial Manager

Senior Clinical Trial Manager (Sr CTM)

Manager, Clinical Operations

Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)

Clinical Trials Manager (Biotechnology, Oncology)

Senior Global Clinical Study Manager

Sr. Clinical Trial Manager

Associate Director/Senior Clinical Trials Manager

Clinical Trials Manager

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