Top 125 Clinical research assistant Jobs in Poway 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
Clinical Research Assistant - Oncology
Scripps Health —La Jolla, CA
- $28.05 - $37.65 an hour
- Full-time
- Hospital
- Bachelor of Science
- BLS Certification
Genetics Staff Research Associate - Psychiatry
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- Part-time
- Remote
- Microsoft Excel
- Psychiatry
- Addiction Medicine
11d
Research Assistant
San Diego Gastroenterology Clinical Research —San Diego, CA
- $23 - $27 an hour
- Full-time
- Research
- High school diploma or GED
- Criminal background check
- Flexible schedule
Quick Apply
Research Assistant - Medicine
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Word processing
- Pass drug screening
- Mid-level
8d
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
4d
Anxiety and Stress Staff Research Associate
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Microsoft Excel
- Psychiatry
- Pass drug screening
Clinical Research Associate
USC —San Diego, CA
- $36.36 - $50.90 an hour
- Background check
- Mid-level
- Bachelor's degree
Research Assistant
Odyssey Systems Consulting Group, Ltd. —San Diego, CA
- $50,000 - $59,890 a year
- Full-time
- Hybrid work
- BLS Certification
- Analysis skills
- Bachelor's degree
- Health savings account
- Paid holidays
10d
Research Assistant
Odyssey Consulting —Naval Medical Center San Diego, CA
- $50,000 - $59,890 a year
- Full-time
- Hybrid work
- BLS Certification
- Analysis skills
- Bachelor's degree
- Health savings account
- Paid holidays
11d
CRA 1, IQVIA Biotech
IQVIA —Carlsbad, CA
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Laboratory Research Assistant - Cancer Center
UC San Diego Health —San Diego, CA
- $28.69 - $35.93 an hour
- 8 hour shift
- Pass drug screening
- Mid-level
- University
CRA 2, Early Clinical Development
IQVIA —Carlsbad, CA
- $90,200 - $150,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Assistant Research Administrator
USC —San Diego, CA
- $36.94 - $47.00 an hour
- Background check
- Microsoft Excel
- Microsoft Access
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
Clinical Research Coordinator
Research site —Vista, CA
- $28 - $31 an hour
- Full-time
- Blood sampling
- Mid-level
- Bachelor's degree
- Health insurance
- Paid time off
Quick Apply
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 Research Assistant/Interviewer - French
UC San Diego Health —San Diego, CA
- $34.58 - $58.41 an hour
- Weekends as needed
- Microsoft Word
- Pass drug screening
- English
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA —San Diego, CA
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
12d
Research Associate
Odyssey Consulting —Naval Medical Center San Diego, CA
- $70,000 - $77,080 a year
- Full-time
- Hybrid work
- BLS Certification
- Mid-level
- Master's degree
- Health savings account
- Paid holidays
11d

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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

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 research assistant jobs in poway ca

Clinical Research Associate, Full Service

Clinical Research Assistant - Oncology

Genetics Staff Research Associate - Psychiatry

Research Assistant

Research Assistant - Medicine

Assistant Clinical Research Coordinator - Psych

Anxiety and Stress Staff Research Associate

Clinical Research Associate

Research Assistant

Research Assistant

CRA 1, IQVIA Biotech

Laboratory Research Assistant - Cancer Center

CRA 2, Early Clinical Development

Assistant Research Administrator

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

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Assistant/Interviewer - French

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

Research Associate

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