Top 15 Clinical study manager Jobs in Carlsbad, Ca

Clinical Research Associate, Full Service
IQVIA —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Carlsbad, CA
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Manager, Clinical Operations
IQVIA —Carlsbad, CA
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Clinical Trial Manager
Viking Therapeutics, Inc. —San Diego, CA
- $110,000 - $140,000 a year
- 6 years
- Office
- Bachelor's degree
Quick Apply
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Carlsbad, CA
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
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
13d
Clinical Trial Operations Lead/Clinical Trial Manager
Merck —San Diego, CA
- $117,000 - $184,200 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Paid holidays
- Health insurance
4d
Clinical Data Associate II
Viking Therapeutics, Inc. —San Diego, CA
- $75,000 - $90,000 a year
- Writing skills
- System design
- Mid-level
Quick Apply
2d
Clinical Data Manager
Viking Therapeutics, Inc. —San Diego, CA
- $110,000 - $120,000 a year
- System design
- Mid-level
- Analysis skills
Quick Apply
2d
Manager, Biomarker Operations
Artiva Biotherapeutics —San Diego, CA
- $130,000 - $142,000 a year
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
Director, Clinical Data Management
Xencor —San Diego, CA
- $195,000 - $240,000 a year
- Full-time
- Hybrid work
- Computer Science
- 5 years
- Bachelor of Science
- Employee stock purchase plan
- Health insurance
Quick Apply
Manager / Senior Manager, Clinical Project Management
Artiva Biotherapeutics —San Diego, CA
- $130,000 - $180,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Organizational skills
- Paid holidays
- Disability insurance
Quick Apply
Principal Scientist / Senior Principal Scientist
Arisan Therapeutics, Inc —Carlsbad, CA
- $150,000 - $205,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- US work authorization
- Paid holidays
- Relocation assistance
Quick Apply
8d

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Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Carlsbad, CA
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
$47,400 - $169,300 a year
Clinical Research Associate
USC —San Diego, CA
Incumbent will provide oversight to the progress of clinical trials at study sites, and ensure that they are conducted, recorded, and reported in accordance…
$36.36 - $50.90 an hour

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Track to ensure that data entry is complete for subjects including completed study visits and related forms. The Data Entry Clerk is responsible for the overall…
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The Ohio State University Wexner Medical Center —Columbus, OH
Partner with operational, clinical, research, and administrative stakeholders to define data requirements and develop reporting solutions that support business…
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Clinical Research Associate, Full Service

IQVIA -
Carlsbad, CA

Apply Now

Job Details

Full-time
$47,400 - $169,300 a year

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Carlsbad, United States of America | Full time | Field-based | R1497311

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.

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

Refine Your Search

clinical study manager jobs in carlsbad, ca

Clinical Research Associate, Full Service

Clinical Research Associate, Full Service

Manager, Clinical Operations

Clinical Trial Manager

Senior Clinical Research Associate, Sponsor Dedicated

Assistant Clinical Research Coordinator - Psych

Clinical Trial Operations Lead/Clinical Trial Manager

Clinical Data Associate II

Clinical Data Manager

Manager, Biomarker Operations

Director, Clinical Data Management

Manager / Senior Manager, Clinical Project Management

Principal Scientist / Senior Principal Scientist

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