Top 2 clinical research associate Jobs in saint augustine fl

Clinical Research Coordinator 1
Rovia Clinical Research —Saint Augustine, FL
- $50,000 - $55,000 a year
- Full-time
- Patient monitoring
- High school diploma or GED
- Bachelor's degree
Quick Apply
7h
Clinical Research Coordinator
ECN Operating LLC —Jacksonville, FL
- Full-time
- Organizational skills
- Communication skills
- Entry level
Quick Apply
10d

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Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…
Experienced Clinical Research Associate - Full-Service
Syneos - Clinical and Corporate - Prod —Ohio
Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of…
$70,100 - $126,100 a year
3d

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Clinical Research Coordinator 1

Rovia Clinical Research
Saint Augustine, FL

Quick Apply

Job Details

Full-time
$50,000 - $55,000 a year
7 hours ago

Qualifications

High school diploma or GED

Full Job Description

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 1 (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.
Resolves data queries and ensures data integrity.
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.

Education/Experience:

High school diploma required, bachelor’s degree in related field preferred.
At least 1 year of clinical research experience.
Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.

The pay range for this role is:
50,000 - 55,000 USD per year(St. Augustine)

Quick Apply

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clinical research associate jobs in saint augustine fl

Clinical Research Coordinator 1

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