Top 31 Clinical trial management associate Jobs in Oceanside, 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 Trial Management Associate
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $88,776 - $133,156 a year
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
Quick Apply
3d
Drug Safety Associate
Viking Therapeutics, Inc. —San Diego, CA
- $77,000 - $90,000 a year
- Nursing
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Clinical Research Associate, Full Service
IQVIA —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Program Supervisor
Olive Crest —San Diego, CA
- $90,000 - $93,000 a year
- Full-time
- LMFT
- Management
- Doctoral degree
- Paid jury duty
- Health savings account
Quick Apply
11d
CRA 1, IQVIA Biotech
IQVIA —Carlsbad, CA
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
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
5d
CRA 2, Early Clinical Development
IQVIA —Carlsbad, CA
- $90,200 - $150,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Distribution Associate
Catalent —San Diego, CA
- $50,000 - $54,000 a year
- Email
- Forklift
- High school diploma or GED
- Ability to lift 50 pounds
- Paid holidays
- Health insurance
Business Intelligence Analyst - ACTRI - Hybrid
UC San Diego Health —San Diego, CA
- $43.39 - $79.69 an hour
- 8 hour shift
- Hybrid work
- Pass drug screening
- System design
- Mid-level
3d
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Carlsbad, CA
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Associate Director, Development Quality Assurance
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $154,500 - $196,873 a year
- Hybrid work
- 5 years
- Writing skills
- Master's degree
Quick Apply
Senior Clinical Research Associate, Sponsor Aligned, Oncology
IQVIA —Carlsbad, CA
- $71,900 - $189,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Financial Analyst III - Medicine - Hybrid
UC San Diego Health —San Diego, CA
- $79,200 - $115,000 a year
- 8 hour shift
- Hybrid work
- Writing skills
- Pass drug screening
- 3 years
13d
Staff Research Associate - Bilingual - RMAS
UC San Diego Health —San Diego, CA
- $28.69 - $35.93 an hour
- 8 hour shift
- Spanish
- Pass drug screening
- English
Director, Administrative Services
UC San Diego Health —San Diego, CA
- $43.39 - $79.69 an hour
- Monday to Friday
- Customer service
- 5 years
- Pass drug screening
Associate Director, Clinical Development - Neurology
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $168,820 - $250,502 a year
- Hybrid work
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
2d
Director, SOM Faculty Programs & Development
UC San Diego Health —San Diego, CA
- $57.18 - $110.54 an hour
- 8 hour shift
- School experience
- 7 years
- Writing skills
Senior Research Associate, MEDSCH/EMERG MED SVC
UC San Diego Health —San Diego, CA
- $36.13 - $58.11 an hour
- 8 hour shift
- Background check
- Pass drug screening
- Surgery
Research Associate II - Manufacturing
Amprion —San Diego, CA
- $70,000 - $85,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Health insurance
- Dental 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 trial management associate jobs in oceanside, ca

Clinical Research Associate, Full Service

Clinical Trial Management Associate

Drug Safety Associate

Clinical Research Associate, Full Service

Clinical Program Supervisor

CRA 1, IQVIA Biotech

Assistant Clinical Research Coordinator - Psych

CRA 2, Early Clinical Development

Distribution Associate

Business Intelligence Analyst - ACTRI - Hybrid

Senior Clinical Research Associate, Sponsor Dedicated

Associate Director, Development Quality Assurance

Senior Clinical Research Associate, Sponsor Aligned, Oncology

Financial Analyst III - Medicine - Hybrid

Staff Research Associate - Bilingual - RMAS

Director, Administrative Services

Associate Director, Clinical Development - Neurology

Director, SOM Faculty Programs & Development

Senior Research Associate, MEDSCH/EMERG MED SVC

Research Associate II - Manufacturing

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