Top 73 Clinical trial manager Jobs in Uc Berkeley Ca

Clinical Trial Manager (Retina)
4D Molecular Therapeutics —Emeryville, CA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- 6 years
- Microsoft Outlook
Clinical Research Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Nursing
- RN License
- BLS Certification
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/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 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
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 Trials Manager- Late Phase Oncology
Gilead Sciences —Foster City, CA
- $133,195 - $189,640 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
Clinical Trial Manager
Sagimet Biosciences —San Mateo, CA
- $90 - $100 an hour
- Hybrid work
- Nursing
- 3 years
- Analysis skills
Research Program Manager
University of California San Francisco —San Francisco, CA
- Full-time
- Medicine
- Surgery
- Research
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
SR. CLINICAL TRIAL MANAGER
Sutro Biopharma —South San Francisco, CA
- $155,000 - $175,000 a year
- Full-time
- Nursing
- Microsoft Outlook
- LVN
Sr Clinical Trials Manager
Gilead Sciences —Foster City, CA
- $157,590 - $203,940 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
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
Clinical Research Manager - Heme Malignancy Program
University of California San Francisco —San Francisco, CA
- Customer service
- Word processing
- 3 years
Senior Project Manager Clinical Research
Abbott Laboratories —Alameda, CA
- $100,000 - $200,000 a year
- Full-time
- Master's degree
- 8 years
- Travel
- Health insurance
- Tuition reimbursement
7d
Clinical Research Supervisor
University of California San Francisco —San Francisco, CA
- Contract
- Word processing
- HIPAA
- Ob/Gyn
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 Program Manager
Arcus Biosciences —Hayward, CA
- $175,000 - $190,000 a year
- Full-time
- 7 years
- Office
- Analysis skills
9d
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 Trials Manager, Biomarker/Bioanalytical Operations
Gilead Sciences —Foster City, CA
- $146,540 - $189,640 a year
- Full-time
- Master's degree
- Databases
- Bachelor's degree
- Health insurance
- Dental 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 uc berkeley ca

Clinical Trial Manager (Retina)

Clinical Research Manager

Clinical Trial Manager, CKD

Clinical Trial Manager/Sr Clinical Trial Manager

Clinical Trials Manager, Early Phase Oncology (Office Based)

Clinical Trial Manager

Clinical Trials Manager- Late Phase Oncology

Clinical Trial Manager

Research Program Manager

Clinical Trials Manager (Biotechnology, Oncology)

SR. CLINICAL TRIAL MANAGER

Sr Clinical Trials Manager

Manager, Clinical Operations

Clinical Research Manager - Heme Malignancy Program

Senior Project Manager Clinical Research

Clinical Research Supervisor

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

Senior Clinical Program Manager

Senior Clinical Trials Manager

Clinical Trials Manager, Biomarker/Bioanalytical Operations

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