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Entry Level Clinical Study Startup Jobs (NOW HIRING)

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

... Study Startup. As a small company, we are highly adaptable, flexible, and transparent. Our ... This is an exciting entry-level opportunity to join a fast-paced and dynamic learning environment ...

Honorhealth

$23.50 - $31.50/hr

... study startup/close out. Serves as a liaison with sponsor. Collects, verifies, organizes, completes and records clinical information and data in case report forms. May be involved in many of the data ...

Cayuse Holdings

Study Coordinator II

Honolulu, HI

$75K - $82K/yr

Align sponsored studies with an appropriate Principal Investigator (PI), taking into account clinical specialty, research interests, and operational feasibility, and coordinate initial study startup ...

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Entry Level Clinical Study Startup information

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

As of Jul 8, 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:
What job categories do people searching Entry Level Clinical Study Startup jobs look for? The top searched job categories for Entry Level Clinical Study Startup jobs are:
Entry Level Clinical Study Startup jobs near you
Infographic showing various Entry Level Clinical Study Startup job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.
Research (Professional)

Research (Professional)

University of Pittsburgh

Pittsburgh, PA • On-site

Full-time

Re-posted 11 days ago

Job description

The Academic Research Center for Hematology (ARCH) at the University of Pittsburgh is seeking a Temporary Clinical Research Coordinator to support clinical research focused primarily on sickle cell disease and other hematological disorders. This role plays a key part in the coordination and execution of investigator-initiated and industry-sponsored clinical studies.
Core Responsibilities:
• Study Coordination: Coordinate day-to-day activities for clinical research studies, including study startup, participant visits, data collection, and study closeout.
• Participant Engagement: Support recruitment, screening, informed consent, scheduling, and retention of research participants.
• Data & Documentation: Maintain accurate study documentation, enter data into study databases, and ensure timely query resolution. Assist with study finance tracking
• Regulatory & Compliance: Assist with IRB submissions, protocol amendments, adverse event reporting, and ensure compliance
• Team Collaboration: Work closely with investigators, clinical staff, sponsors, and research team members to support high-quality, patient-centered research.

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