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Entry Level Clinical Study Startup Jobs in Raleigh, NC

410 ICR United States USA

Contract Analyst I

Raleigh, NC

$67K - $81K/yr

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 ...

Bruno

Clinical Payments Specialist

Raleigh, NC · On-site +1

Clinical Budget Specialist Clinical Research Location: Remote (United States) Employment Type ... Manage study-specific global investigator budget processes from study startup through closeout.

Bruno

Clinical Payments Specialist

Raleigh, NC · Remote

Clinical Budget Specialist Clinical Research Location: Remote (United States) Employment Type ... Manage study-specific global investigator budget processes from study startup through closeout.

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

ECLARO

Clinical Research Coordinator

Chapel Hill, NC · On-site

$20.25 - $26.75/hr

Independently manage multiple oncology clinical trials from startup through study closeout. * Maintain a comprehensive understanding of assigned study protocols and sponsor requirements. * Coordinate ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Prism Biotech, Inc

Pharma Detail Agent Rep

Raleigh, NC · On-site

$87K - $119K/yr

Ability to comprehend knowledge of products, clinical studies, protocols and guidelines and ... entry level * Ability to understand and communicate highly scientific and technical medical ...

Prism Biotech

Pharma Detail Agent Rep

Raleigh, NC · On-site

$87K - $119K/yr

Ability to comprehend knowledge of products, clinical studies, protocols and guidelines and ... entry level * Ability to understand and communicate highly scientific and technical medical ...

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Entry Level Clinical Study Startup information

See Raleigh, NC salary details

$11

$36

$66

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

As of Aug 8, 2026, the average hourly pay for entry level clinical study startup in Raleigh, NC is $36.62, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.73 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.

What are the most commonly searched types of Clinical Study Startup jobs in Raleigh, NC? The most popular types of Clinical Study Startup jobs in Raleigh, NC are:
What are popular job titles related to Entry Level Clinical Study Startup jobs in Raleigh, NC? For Entry Level Clinical Study Startup jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Entry Level Clinical Study Startup jobs in Raleigh, NC look for? The top searched job categories for Entry Level Clinical Study Startup jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Clinical Study Startup jobs? Cities near Raleigh, NC with the most Entry Level Clinical Study Startup job openings:
Entry Level Clinical Study Startup jobs near you
Infographic showing various Entry Level Clinical Study Startup job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $76,160 per year, or $36.6 per hour.

Contract Analyst I

410 ICR United States USA

Raleigh, NC

$67K - $81K/yr

Full-time

Posted 4 days ago

Job description

Contract Analyst I

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Contract Analyst I at ICON, you will prepare, verifying, and carrying out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts.

What You Will Do:

You will contribute to contract management activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements and amendments.
  • 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 across projects.
  • Leverage leading industry tools and data sources to provide budget and contract feedback aligned with parameters and fair market value guidance.
  • Promptly recognize and improve potential delays and escalate to appropriate team members.
  • Track all actions and negotiations to ensure timelines are achieved for studies and sites assigned.
  • Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team.

Your Profile:

You will bring relevant contract management experience, along with the following qualifications and skills.
Required qualifications and experience:

  • BS degree or international equivalent
  • 2 or more years of experience in clinical research site contracting and budgeting within a pharmaceutical company, CRO or relevant industry vendor.
  • Ability to explain data to facilitate decision making processes to be data driven.
  • Knowledge and understanding of clinical study protocols and schedule of assessments 
  • Strong organizational skills, decision making, communication and negotiation skills.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply