Top 67 Clinical research associate Jobs in San Marcos 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 Associate, Full Service
IQVIA —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Carlsbad, CA
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Research Coordinator II
Iterative Health —San Marcos, CA
- Patient monitoring
- HIPAA
- Mid-level
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
CRA 2/Senior CRA
IQVIA —Carlsbad, CA
- $87,200 - $169,300 a year
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
CRA 2/Senior CRA 1
IQVIA —Carlsbad, CA
- $90,200 - $175,100 a year
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
Logistics & Recruitment Clinical Research Coordinator (LVN or RN Preferred)
San Diego Cardiac Center Medical Group Inc —San Diego, CA
- $37 - $45 an hour
- Full-time
- Nursing
- Current TB test
- LVN
- Health insurance
- Dental insurance
Quick Apply
12d
Clinical Research Recruiter (Patient Recruitment Specialist)
Clinical Research Dermatology —Encinitas, CA
- From $23 an hour
- Full-time
- Medical office experience
- High school diploma or GED
- Organizational skills
Quick Apply
CRA 2, Early Clinical Development
IQVIA —Carlsbad, CA
- $90,200 - $150,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Contractor- Assistant Clinical Research Coordinator (Oceanside, CA)
Profound Research —Oceanside, CA
- Full-time
- Vital signs
- Urgent Care
- Clinic experience
- Health insurance
- Paid time off
Quick Apply
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Temecula, CA
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
Manager, Clinical Operations
IQVIA —Carlsbad, CA
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Clinical Data Specialist II
Alphatec Spine —Carlsbad, CA
- $85,000 - $98,000 a year
- Full-time
- Mid-level
- SQL
- Analysis skills
Quick Apply
Research Assistant
San Diego Cardiac Center Medical Group Inc —San Diego, CA
- $22 - $25 an hour
- 8 hour shift
- Computer literacy
- Organizational skills
- Medical terminology
- Health insurance
- Dental insurance
Quick Apply
10d
Clinical Data Associate II
Viking Therapeutics, Inc. —San Diego, CA
- $75,000 - $90,000 a year
- Writing skills
- System design
- Mid-level
Quick Apply
23h
Contractor- Clinical Research Coordinator (Oceanside, CA)
Profound Research —Oceanside, CA
- Full-time
- Patient monitoring
- Urgent Care
- Clinic experience
- Health insurance
- Paid time off
Quick Apply
Clinical Research Coordinator
Medical Oncology Associates of San Diego —San Diego, CA
- $70,000 - $80,000 a year
- 8 hour shift
- Patient monitoring
- Bachelor of Science
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
FSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West Coast
Thermo Fisher Scientific —San Diego, CA
- $85,000 - $120,000 a year
- Full-time
- Background check
- Nursing
- RN License
- Commuter assistance
- Paid parental leave
Senior Clinical Research Coordinator
Platinum Dermatology Partners LLC —San Diego, CA
- $38 - $41 an hour
- Full-time
- Computer literacy
- Mid-level
- 3 years
- Paid holidays
- Disability insurance
Quick Apply

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Clinical Research Associate, Full Service

5PY IQVIA RDS Inc. -
Carlsbad, CA

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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 associate jobs in san marcos ca

Clinical Research Associate, Full Service

Clinical Research Associate, Full Service

Senior Clinical Research Associate, Sponsor Dedicated

Clinical Research Coordinator II

Clinical Research Coordinator

CRA 2/Senior CRA

CRA 2/Senior CRA 1

Logistics & Recruitment Clinical Research Coordinator (LVN or RN Preferred)

Clinical Research Recruiter (Patient Recruitment Specialist)

CRA 2, Early Clinical Development

Contractor- Assistant Clinical Research Coordinator (Oceanside, CA)

Per Diem Clinical Research Nurse - Home Visits

Manager, Clinical Operations

Clinical Data Specialist II

Research Assistant

Clinical Data Associate II

Contractor- Clinical Research Coordinator (Oceanside, CA)

Clinical Research Coordinator

FSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West Coast

Senior Clinical Research Coordinator

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