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Study Startup Associate Jobs (NOW HIRING)

As the Clinical Research Associate I you will assist in the clinical execution and management of ... Responsible for assisting senior study startup staff during site selection * Maintain and audit ...

As the Clinical Research Associate I you will assist in the clinical execution and management of ... Responsible for assisting senior study startup staff during site selection * Maintain and audit ...

Support study startup activities, including site feasibility, onboarding, and activation of ... Associate (CRA) or in a comparable clinical research role. * 3 or more years experience supporting ...

Support study startup activities, including site feasibility, onboarding, and activation of ... Associate (CRA) or in a comparable clinical research role. * 3 or more years experience supporting ...

... Study Startup. As a small company, we are highly adaptable, flexible, and transparent. Our ... Clinical Operations Associate: $70,304 - 80,000 annually + benefits package and annual performance ...

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As of Sep 10, 2026, the average hourly pay for study startup associate in the United States is $19.87, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $20.67 per hour, depending on experience, location, and employer.

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Infographic showing various Study Startup Associate job openings in the United States as of September 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 77% In-person, 8% Hybrid, and 15% Remote job distribution, with an average salary of $41,327 per year, or $19.9 per hour.

Clinical Research Associate I

Alameda, CA • On-site

$73K - $116K/yr

Full-time

Re-posted 7 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz


Job 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 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
The Opportunity
This position works out of our Alameda, CA location in the Diabetes Care division where we're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
As the Clinical Research Associate I you 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.
What You'll Work On
  • Participate in study start up activities, to include but not limited to, conducting investigator debarment checks, collection of regulatory documents and preparing the study files.
  • Conduct Site Qualification Visits (SQV) and reporting to ensure study staff and research site are adequate to perform ADC trials.
  • Assist with shipment of study devices and supplies to clinical sites and maintain communication with the device group as required.
  • Responsible for assisting senior study startup staff during site selection
  • Maintain and audit Trial Master File and upload to Veeva Vault to ensure inspection readiness.
  • Proactively and effectively communicate the status of clinical trial start up to management.
  • Support regulatory submissions
  • In addition, you may be asked to perform any other duties as assigned by management.

Required Qualifications
  • BS degree in life sciences preferred, with two years of experience as a CRC/CTA or combination of appropriate education and experience.
  • Experience in conducting medical device studies preferred, pharmaceutical background may also be considered.
  • Perform any other duties as assigned by management.

Preferred Qualifications
  • Demonstrated excellence in teamwork, stellar interpersonal and communication skills including building rapport with team members, peers, and management.
  • Working knowledge of GCP, Clinical and Regulatory Affairs.
  • Flexibility in daily activities.
  • Proficient with Microsoft Suite

The base pay for this position is
$73,900.00 - $116,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Research and Discovery
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : Plaza 6 Building
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 15 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
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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