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Entry Level Clinical Study Startup 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 ...

$59K - $71K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA · On-site

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA · On-site

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA · On-site +1

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

$59K - $71K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

$70K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA · On-site +1

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

$59K - $71K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Raleigh, NC · On-site

$67K - $81K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Contract Analyst I

Blue Bell, PA

$65K - $79K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. * Ensure standards are applied to the SB&C processes ...

Showing results 21-40

Entry Level Clinical Study Startup information

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How much do entry level clinical study startup jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for entry level clinical study startup in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Clinical Study Startup vs Clinical Research Coordinator?

AspectEntry Level Clinical Study StartupClinical Research Coordinator
CredentialsBachelor's degree, training in clinical trial processesBachelor's degree, often with certification in clinical research
Work EnvironmentPrepares sites, manages startup documentation, coordinates with teamsOversees patient recruitment, data collection, and site activities
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

Entry Level Clinical Study Startup roles focus on preparing clinical sites for trials, including documentation and regulatory submissions. Clinical Research Coordinators manage patient interactions and data during the trial. Both roles require similar educational backgrounds but differ in daily responsibilities and focus areas within the clinical research process.

More about Entry Level Clinical Study Startup jobs

What cities are hiring for Entry Level Clinical Study Startup jobs?

Cities with the most Entry Level Clinical Study Startup job openings:

What are the most commonly searched types of Clinical Study Startup jobs?

The most popular types of Clinical Study Startup jobs are:

What states have the most Entry Level Clinical Study Startup jobs?

States with the most job openings for Entry Level Clinical Study Startup jobs include:

Infographic showing various Entry Level Clinical Study Startup job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Research Associate I

Abbott

Alameda, CA • On-site

$73K - $116K/yr

Full-time

Re-posted 14 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

176th of 540 rated manufacturers


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 DiscoveryDIVISION:ADC Diabetes CareLOCATION:United States > Alameda : Plaza 6 BuildingADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 15 % of the TimeMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT 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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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