Top 70 Clinical project manager Jobs in Scripps Ranch Ca

Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
7d
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
Disease Team Project Manager - Cancer Center
UC San Diego Health —San Diego, CA
- $46.55 - $87.16 an hour
- 8 hour shift
- Hybrid work
- 5 years
- Word processing
- Pass drug screening
3d
Project Manager – Clinical Projects - San Diego
PolyPeptide US —San Diego, CA
- $79,000 - $84,000 a year
- Full-time
- Management
- Mid-level
- 3 years
Project/Program Manager 3 - Medical Education & Training (522)
Natus Medical Incorporated —San Diego, CA
- $75,000 - $90,000 a year
- Full-time
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Continuing education credits
- Paid holidays
13d
Sr. Manager, Healthcare Transformation, Brain Health
West Health —San Diego, CA
- $165,000 - $185,000 a year
- Full-time
- Hybrid work
- Psychiatry
- 5 years
- Office
- Paid holidays
- Disability insurance
Sr. Manager, Healthcare Transformation, Digital Health
West Health —San Diego, CA
- $165,000 - $185,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Paid holidays
- Disability insurance
Project Manager - Hybrid
UC San Diego Health —San Diego, CA
- $37.47 - $60.30 an hour
- 8 hour shift
- Hybrid work
- Pass drug screening
- English
- Mid-level
13d
Manager/Sr. Manager, Clinical GCP Quality Assurance
Rakuten Medical Inc. - US —San Diego, CA
- $150,000 - $170,000 a year
- Full-time
- Remote
- Bachelor of Science
- English
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Project Manager
9290 FCX Performance, Inc. —San Diego, CA
- $48 - $55 an hour
- Full-time
- Clean driving record
- 5 years
- Engineering
15h
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
3d
Project Manager - Strategic Support
Family Health Centers of San Diego —San Diego, CA
- $80,000 - $120,000 a year
- Full-time
- Clean driving record
- Microsoft Excel
- Microsoft Outlook
- Paid holidays
- 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
Senior Clinical Trial Manager, Clinical Operations
Iambic Therapeutics, Inc —San Diego, CA
- $152,000 - $190,000 a year
- Full-time
- 7 years
- Bachelor's degree
- Travel
- Flexible spending account
- 401(k) matching
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
Implementation Project Manager
XIFIN —San Diego, CA
- $80,000 - $125,000 a year
- Full-time
- Office
- Bachelor's degree
- Travel
- Wellness program
- Health savings account
Quick Apply
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
15h
Project manager
Sherpa Clinical Packaging —San Diego, CA
- Mid-level

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Clinical Research Associate, Full Service

5PY IQVIA RDS Inc. -
Carlsbad, CA

Apply Now

Job Details

Full-time
$47,400 - $169,300 a year
7 days ago

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Some organizations require completion of CRA training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $47,400.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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Refine Your Search

clinical project manager jobs in scripps ranch ca

Clinical Research Associate, Full Service

Supervising Clinical Operations Project Manager

Clinical Trial Manager/Sr Clinical Trial Manager

Disease Team Project Manager - Cancer Center

Project Manager – Clinical Projects - San Diego

Project/Program Manager 3 - Medical Education & Training (522)

Sr. Manager, Healthcare Transformation, Brain Health

Sr. Manager, Healthcare Transformation, Digital Health

Project Manager - Hybrid

Manager/Sr. Manager, Clinical GCP Quality Assurance

Project Manager

Clinical Compliance Manager

Project Manager - Strategic Support

Clinical Trial Manager

Manager, Clinical Operations Consultant

Senior Clinical Trial Manager, Clinical Operations

Document and Clinical Systems Manager

Implementation Project Manager

Sr. Manager, Clinical Quality Assurance

Project manager

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