Top 8 Senior research associate Jobs in Carlsbad Ca

Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Carlsbad, CA
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Senior Research Associate/Senior Scientist, Pharmaceutical Development
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $87,000 - $154,461 a year
- Hybrid work
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
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
Senior Research Associate, Discovery Biology
ADARx Pharmaceuticals Inc. —San Diego, CA
- $75,000 - $85,000 a year
- Full-time
- Background check
- 5 years
- Bachelor of Science
- Paid jury duty
- Paid holidays
Quick Apply
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
Sr. Research Associate/Associate Scientist, Immunology (Contract)
Vividion Therapeutics, Inc —San Diego, CA
- $38 - $48 an hour
- Contract
- Bachelor of Science
- Bachelor's degree
- US work authorization
Quick Apply
17h

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Associate Director, In-Vivo Pharmacology
Bristol-Myers Squibb —San Diego, CA
This role provides functional leadership to senior scientists to design and execute high‑quality in‑vivo studies that inform program strategy from discovery…
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Associate Scientist I, In Vivo Research
Arrowhead Pharmaceuticals —San Diego, CA
BS and/or MS in biology related field. Present research findings to project teams and prepare technical reports. Perform animal behavior studies as needed.
$65,000 - $75,000 a year

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Senior Clinical Research Associate, Sponsor Dedicated

IQVIA -
Carlsbad, CA

Apply Now

Job Details

Full-time
$74,500 - $197,500 a year

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Carlsbad, United States of America | Full time | Field-based | R1555319

External Job Description

To be eligible for this position, you must reside in the same country where the job is located.

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 Good Clinical Practice.
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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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.
Requires at least 3 years of year of on-site monitoring experience.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Good 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 $74,500.00 - $197,500.00. 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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

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senior research associate jobs in carlsbad ca

Senior Clinical Research Associate, Sponsor Dedicated

Senior Research Associate/Senior Scientist, Pharmaceutical Development

Senior Clinical Research Associate, Sponsor Aligned, Oncology

Senior Research Associate, Discovery Biology

Senior Research Associate, MEDSCH/EMERG MED SVC

Sr. Research Associate/Associate Scientist, Immunology (Contract)

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