Top 44 Clinical study manager Jobs in San Diego, Ca

Supervising Clinical Operations Project Manager
USC —San Diego, CA
- $140,572.82 - $183,825.50 a year
- Background check
- 5 years
- Master's degree
Clinical Trial Manager/Sr Clinical Trial Manager
Erasca —San Diego, CA
- $145,000 - $190,000 a year
- Remote
- Medicine
- Inventory management
- 5 years
- Health savings account
- AD&D insurance
Clinical Research Coordinator (Non-RN) - Research & Clinical Management - Genomics (In-Person Role)
Rady Children's Health —San Diego, CA
- $34.14 - $46.94 an hour
- Vital signs
- Management
- Word processing
3d
Senior Manager, Clinical Operations
Travere Therapeutics —San Diego, CA
- $132,000 - $172,000 a year
- Online Application
- Microsoft Office
- Bachelor's degree
- Travel
- Health insurance
- Paid time off
10d
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
Rady Children's Health —San Diego, CA
- $34.14 - $46.94 an hour
- Vital signs
- Management
- Word processing
Document and Clinical Systems Manager
Neurocrine Bioscience —San Diego, CA
- $130,800 - $179,000 a year
- Full-time
- Psychiatry
- Computer literacy
- Bachelor of Science
- Paid holidays
- Health insurance
Clinical Research Coordinator I
CAMRIS International, LLC —San Diego, CA
- $70,304 - $73,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Mid-level
- Health savings account
- AD&D insurance
Clinical Compliance Manager
Neurocrine Bioscience —San Diego, CA
- $130,800 - $179,000 a year
- Full-time
- Psychiatry
- Bachelor of Science
- Master's degree
- Paid holidays
- Health insurance
Clinical Trials Manager
Neurocrine Bioscience —San Diego, CA
- $130,800 - $179,000 a year
- Full-time
- Psychiatry
- Computer literacy
- Bachelor of Science
- Paid holidays
- Health insurance
2d
QA Manager, GCP
Sobi —San Diego, CA
- $112,000 - $153,000 a year
- Full-time
- Hybrid work
- 5 years
- Senior level
- Health insurance
Quick Apply
Clinical Trial Manager
Viking Therapeutics, Inc. —San Diego, CA
- $110,000 - $140,000 a year
- 6 years
- Office
- Bachelor's degree
Quick Apply
Manager, Clinical Operations Consultant
RegDev —San Diego, CA
- Full-time
- Writing skills
- Office
- Master's degree
Clinical Trial Operations Lead/Clinical Trial Manager
Merck —San Diego, CA
- $117,000 - $184,200 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Paid holidays
- Health insurance
5d
Clinical Data Manager
Viking Therapeutics, Inc. —San Diego, CA
- $110,000 - $120,000 a year
- System design
- Mid-level
- Analysis skills
Quick Apply
2d
Sr. Clinical Trials Manager
Neurocrine Bioscience —San Diego, CA
- $156,900 - $214,000 a year
- Full-time
- 6 years
- Psychiatry
- Computer literacy
- Paid holidays
- Health insurance
2d
Sr Clinical Research Coord Non-RN - Hematology Oncology Research Resources
Rady Children's Health —San Diego, CA
- $37.63 - $51.75 an hour
- Bilingual
- Management
- Master's degree
Specialist, Clinical Trial Operations
Neurocrine Bioscience —San Diego, CA
- $89,800 - $123,000 a year
- Full-time
- Psychiatry
- Computer literacy
- Bachelor of Science
- Paid holidays
- Health insurance
11d
Project Manager - Pediatrics
UC San Diego Health —San Diego, CA
- 8 hour shift
- Writing skills
- Pass drug screening
- 3 years
3d
Assistant Clinical Research Coordinator - Psych
UC San Diego Health —San Diego, CA
- $36.31 - $58.41 an hour
- 8 hour shift
- Microsoft Word
- Psychiatry
- Addiction Medicine
13d
Sr. Manager, Clinical Quality Assurance
Artiva Biotherapeutics —San Diego, CA
- $150,000 - $172,000 a year
- Full-time
- Remote
- Microsoft Excel
- Management
- Bachelor of Science
- Paid holidays
- Disability insurance
Quick Apply

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Supervising Clinical Operations Project Manager

USC -
San Diego, CA

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Job Details

$140,572.82 - $183,825.50 a year

Qualifications

Managing scientific research projects
Finance
Technical documentation
Spreadsheets
Data summary reports
ICH guidelines
Supervising experience
Records management
Team management
Pharmaceutical company experience
Managing clinical research teams
Computer skills
Managing projects
Technical writing experience within technology
Pharmaceutical research experience
Medical terminology

Full Job Description

The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute comprised of an expert panel of scientific collaborators, committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.

The ATRI is seeking a motivated, dependable, and experienced Supervising - Project Manager to support ATRI clinical research efforts. This is a highly visible role, responsible for managing the successful execution of ATRI clinical trials. Responsibilities include, but are not limited to:

Responsible for supervising and managing a team of Project Managers and Coordinators
Serves as the guidance expert for assigned studies and is the first line of escalation
Collaborate with the Project Director and other functional groups in the planning and administration of all phases of multi-site clinical trials
Set and maintain priorities and timelines for project implementation, maintenance, and closeout of clinical trials across multiple national and international ATRI clinical trial study sites
Conduct and drive study planning meetings including the management of meeting minutes, logging action items and decisions, and tracking action items to completion
Development of various study materials including protocol, training and procedures manuals, source documents, and work instruction documents
Development of templates and guidelines, informed by regulations, policies, and standard operating procedures (SOPs) for the management of assigned studies, as well as departmental initiatives aimed at improving process and efficiency

The ideal candidate will have excellent interpersonal skills for communicating with all levels of personnel and groups and demonstrated ability to successfully operationalize and manage all clinical trial components.

Five years of experience in clinical trials is required as well as a history of supervising staff.

Location: San Diego, CA

The annual base salary range for this position is $140,572.82 - $183,825.50. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.

Minimum Education: Associate's degree Or Bachelor's degree Bachelor's degree Biological Science Or Bachelor's degree Biomedical Sciences Or Bachelor's degree in related field(s) Additional Education Requirements Combined experience/education as substitute for minimum education Minimum Experience: 5 years in on-site clinical trial monitoring. Minimum Skills: Industry experience in a pharmaceutical, biotechnology, clinical research organization and/or nursing setting. Demonstrated experience supervising others, using medical devices and terminology, and managing study records, finances and vendors. Theoretical understanding of health sciences research and ICH-GCP guidelines, with experience applying policies and procedures. Skilled at technical documentation and writing, and at assembling, organizing and conceptualizing numerical data in spreadsheets, databases, reports and presentations. Ability to manage and prioritize different tasks and projects, with deft interpersonal skills for communicating with all levels of staff and various individuals and groups coordinating and executing study activities. Preferred Education: Master's degree Neurosciences Or Master's degree Public Health Or Master's degree Pharmacology Master's degree in related field(s) Preferred Certifications: Certified Clinical Research Associate - CCRA Certified Clinical Research Professional - CCRP Certified Clinical Research Coordinator - CCRC Preferred Experience: 8 years Preferred Skills: Excellent written and verbal communication skills to express complex ideas to study staff at research and clinical institutions. Ability to handle several priorities within multiple, complex clinical trials. Strong understanding of current GCP guidelines applicable to the clinical research conduct. Proficient in OmniPlan or other timeline applications. Familiarity with academic medical centers.

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Refine Your Search

clinical study manager jobs in san diego, ca

Supervising Clinical Operations Project Manager

Clinical Trial Manager/Sr Clinical Trial Manager

Clinical Research Coordinator (Non-RN) - Research & Clinical Management - Genomics (In-Person Role)

Senior Manager, Clinical Operations

Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources

Document and Clinical Systems Manager

Clinical Research Coordinator I

Clinical Compliance Manager

Clinical Trials Manager

QA Manager, GCP

Clinical Trial Manager

Manager, Clinical Operations Consultant

Clinical Trial Operations Lead/Clinical Trial Manager

Clinical Data Manager

Sr. Clinical Trials Manager

Sr Clinical Research Coord Non-RN - Hematology Oncology Research Resources

Specialist, Clinical Trial Operations

Project Manager - Pediatrics

Assistant Clinical Research Coordinator - Psych

Sr. Manager, Clinical Quality Assurance

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