787 matching jobs for “Senior Clinical Research Associate”

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Netherlands

Remote, Netherlands

Join Us as a (Senior) Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported …

Added Oct 16, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Carlsbad, California, United States +2 locations

Pay posted by employer$90,200–$175,100

… initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate (Sr CRA)

Remote, Egypt

… to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate, you'll conduct on-site or remote visits to assess protocol and regulatory compliance and manage required …

Added Oct 20, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Durham, North Carolina, United States

Pay posted by employer$87,200–$169,300

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, Mexico +1 location 3 postings

… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …

Added Oct 20, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, Mexico +1 location 4 postings

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate

Remote, North Carolina, USA 2 postings

Sr CRA (Level I) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory …

Added Oct 28, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate (CRA)

Hong Kong, Hong Kong +1 location

… 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 …

Added Oct 15, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate (CRA)

Taipei, Taiwan

… 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, …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate I

Auckland, Auckland, New Zealand +1 location

… cures for cancer. Location/Division Specific Information Performs and coordinates different aspects of the clinical monitoring and site management process. This home-based position requires candidates to currently be …

Added Oct 25, 2026

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IQVIA Holdings

Clinical Research Associate(Clinical Core)

Seoul, Republic of Korea

… a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: - A Bachelor's degree in a health care or other …

Added Oct 15, 2026

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Thermo Fisher Scientific

Associate Clinical Research Manager

Austin, Texas, United States

Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation The Associate Clinical Research …

Added Oct 25, 2026

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Thermo Fisher Scientific

Clinical Research Associate I

Remote, Singapore

Job Description Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top …

Added Oct 19, 2026

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Abbott Laboratories

Clinical Research Associate II

Alameda, California, United States

Pay posted by employer$81,500–$141,300

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for …

Added Oct 27, 2026

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Abbott Laboratories

Clinical Research Associate I

Alameda, California, United States

Pay posted by employer$73,900–$116,000

Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for …

Added Oct 25, 2026

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Thermo Fisher Scientific

FSP Sr Clinical Research Associate I

Vietnam, Vietnam

Job Description Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Abbott Laboratories

Associate I Clinical Research

Alameda, California, United States

Pay posted by employer$73,900–$116,000

… female executives, and scientists. The Opportunity The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal …

Added Oct 28, 2026

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IQVIA Holdings

Senior Clinical Research Associate - Sponsor Dedicated

Amsterdam, The Netherlands

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model …

Added Oct 15, 2026

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IQVIA Holdings

Senior/Clinical Research Associate (Client Dedicated)

Ho Chi Minh City, Vietnam

… with a variety of colleagues and customers . You will need to have a good knowledge of applicable clinical research regulatory requirements. Qualifications: University degree in scientific discipline or healthcare …

Added Oct 15, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Sponsor Dedicated

Carlsbad, California, United States +1 location

Pay posted by employer$74,500–$197,500

Added Oct 15, 2026

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Abbott Laboratories

Clinical Research Associate II

Alameda, California, United States

Pay posted by employer$81,500–$141,300

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Required Qualifications · employer excerpt

B.S. degree in life sciences or equivalent with minimum 5 years of clinical research experience.
Must have 2+ years of relevant experience in site monitoring.
Experience in conducting medical device and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
Must be able to travel 30-50%.

About this opportunity

Original employer description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Clinical Research Associate II

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards.

This position will be based in our Alameda, CA office.

What You’ll Work On

Conduct single or multi-center medical device clinical studies.
Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items.
Participate in study start up activities.
Responsible for shipping study devices and supplies to clinical sites and performing study device accountability.
Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures and applicable regulatory requirements.
Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
Maintain and audit Trial Master File to ensure inspection readiness.
Perform review of clinical data listings for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed.
Participate in cross-functional clinical team(s) in the planning and execution of clinical trials.
Proactively and effectively communicate the status of clinical studies to management.
Ensures quality delivery of study deliverables within agreed budgets and timelines.
Participate in the interim and final reviews of study data in preparation of regulatory submissions.
Involved in the preparation of all applicable documents required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports).
May interact with RA/QA in responding to audits and FDA inquiries.

Required Qualifications

B.S. degree in life sciences or equivalent with minimum 5 years of clinical research experience.
Must have 2+ years of relevant experience in site monitoring.
Experience in conducting medical device and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
Must be able to travel 30-50%.

Preferred Qualifications

Demonstrated excellence in teamwork, shared mindset for success, stellar interpersonal and communication skills including building rapport with team members, peers, and management.
Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
Must have a demonstrated ability to solve problems with innovative solutions along with strong project management and organizational skills to deliver projects on time and on budget.
Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.
Working knowledge of GCP, Clinical and Regulatory Affairs.
Proficient with Microsoft Suite.

The base pay for this position is

$81,500.00 – $141,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Medical & Scientific Affairs

DIVISION:

ADC Diabetes Care

LOCATION:

United States > Alameda : Plaza 6 Building

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 25 % of the Time

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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