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Clinical Research Study Startup Jobs (NOW HIRING)

Universal Axon Clinical Research, LLC

$18 - $23.75/hr

Clinical Research Coordinator [Bilingual] About Us At Rovia Clinical Research, we're on a mission ... This role partners closely with site teams to support study startup, enrollment, data quality, and ...

ClariMed, Inc.

PA · On-site

Participant Recruitment & Study Startup Manager About ClariMed, Inc. ClariMed is a human-centered ... Experience in participant recruitment, human factors research, clinical research, market research ...

Insight

Clinical Research Coordinator I (CRC-1)

Chicago, IL · On-site

$25 - $33.25/hr

Coordinate site preparation, study startup, participant screening, enrollment, and follow-up visits ... Clinical research certification (CCRC, CCRP) eligible; certification expected within 18 months of ...

United-Digestive

Clinical Research Manager

Atlanta, GA · On-site

Demonstrated experience managing study startup, site activation, conduct, monitoring, closeout, and ... Master's degree in clinical research, healthcare administration, public health, nursing, or a ...

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Clinical Research Study Startup information

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$49K

$107.3K

$189K

How much do clinical research study startup jobs pay per year?

As of Sep 13, 2026, the average yearly pay for clinical research study startup in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

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

AspectClinical Research Study StartupClinical Research Coordinator
Primary RoleInitiates and prepares clinical trial sites for study activation, including regulatory submissions and site readiness.Manages daily trial activities at the site, including patient recruitment, data collection, and compliance.
Required CredentialsOften requires a bachelor's degree in health or life sciences; certifications like CCRP are common.Typically requires a bachelor's degree; certifications like CCRP or CRC are beneficial.
Work EnvironmentWorks closely with sponsors, CROs, and regulatory bodies during study startup phases.Works directly with patients, investigators, and site staff during the trial conduct.

While both roles are essential in clinical research, Study Startup focuses on preparing and initiating trials, whereas a Clinical Research Coordinator manages ongoing trial activities at the site.

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Clinical Research Study Startup jobs near you

Clinical Research Coordinator [Bilingual]

On-site

Universal Axon Clinical Research, LLC
See more jobs at Universal Axon Clinical Research, LLCexternal

$18 - $23.75/hr

Other

Posted 10 days ago

Job description

Clinical Research Coordinator [Bilingual] About Us

At Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

Key Responsibilities:
  • Conducts and coordinates patient visits in accordance with study protocols.
  • Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
  • Ensures informed consent is properly obtained and documented.
  • Educates and guides participants through the study, ensuring a positive patient experience.
  • Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
  • Completes timely and accurate source documentation and EDC data entry.
  • Maintains investigational product accountability and proper storage and handling.
  • Prepares for and supports monitoring visits, audits, and inspections.
  • Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
  • Perform other duties as assigned.
Skills/Abilities:
  • Strong knowledge of medical terminology and clinical procedures.
  • Understanding of ICH/GCP and regulatory requirements.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and patient-facing communication skills.
  • Ability to multitask and manage competing priorities in a fast-paced environment.
  • Proficiency in Microsoft Office, EDC, and CTMS applications.
  • Ability to work both independently and collaboratively.
  • High level of professionalism and commitment to patient confidentiality.
  • Fluent in English and Spanish.
Education/Experience:
  • High school diploma required, bachelor’s degree in related field preferred.
  • 2+ years of clinical research experience.
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