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Vision Research Cro Jobs (NOW HIRING)

Segal Trials

Clinical Research Coordinator

Lauderhill, FL · On-site

$24 - $32/hr

... vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of ... CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the ...

K2 Staffing LLC

Research Assistants

Maitland, FL · On-site

$18 - $24.75/hr

Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

Segal Trials

Clinical Research Coordinator

Hollywood, FL · On-site

$22.25 - $29.50/hr

... vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of ... CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the ...

K2 Staffing LLC

Research Assistant

Maitland, FL · On-site

$18 - $24.75/hr

Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

K2 Staffing LLC

Community Research Coordinator

Ocala, FL · On-site

$50K - $55K/yr

Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

START Research

$59 - $73/hr

Communicate on a regular basis with Study Sponsor's, CRO's, staff, etc. regarding questions ... Comprehensive medical, dental, and vision coverageand optional insuranceoptions * Companyp‑aid ...

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All Jobsvision research JobsVision Research Cro Jobs

Vision Research Cro information

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$43K

$105.3K

$155.5K

How much do vision research cro jobs pay per year?

As of Sep 5, 2026, the average yearly pay for vision research cro in the United States is $105,259.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $127,500.00 per year, depending on experience, location, and employer.

What is the difference between Vision Research Cro vs Vision Research Coordinator?

AspectVision Research CroVision Research Coordinator
CredentialsTypically requires a background in clinical research, regulatory knowledge, and industry-specific certificationsRequires similar research experience, often with additional project management or coordination certifications
Work EnvironmentWorks with CRO teams, clinical trial sites, and sponsors in a regulated industry settingCoordinates clinical trial activities at sites, liaising between investigators and sponsors
Employer & Industry UsageHired by pharmaceutical or biotech companies, CROs, and research organizationsEmployed by research sites, hospitals, or clinical research organizations

While both roles involve clinical research in the vision industry, a Vision Research Cro focuses on managing and overseeing clinical trials for sponsors, whereas a Vision Research Coordinator handles the day-to-day coordination at trial sites. Understanding these differences helps in choosing the right career path or job search focus.

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Vision Research Cro jobs near you
Infographic showing various Vision Research Cro job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $105,259 per year, or $50.6 per hour.

Clinical Research Coordinator

Segal Trials

North Miami Beach, FL • On-site

$23.75 - $31.75/hr

Other

Posted 14 days ago

Key responsibilities

  • Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.

  • Collect, review, and manage participant health data and medical documentation to determine protocol eligibility.

  • Perform clinical tasks such as vital signs, ECG, phlebotomy, specimen processing, and maintain accurate records of investigational products.

Job description

The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned trials. The CRC follows study specific protocol guideline and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done in accordance with company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable local, state, and federal regulations.

Primary Responsibilities

· Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.

· Identify potential problems or inconsistencies and take action as appropriate.

· Articulate protocol issues to CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the study team.

· Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources.

· Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator.

· Ensure a flow of communication including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and/or CRO, Monitor(s) and Auditors, if applicable.

· Perform clinical tasks including, but not limited to vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging.

· Dispense and maintain accurate records of investigational and study product.

· Educate subject and family members regarding specific studies and clinical drug trials in general.

· Complete all monitor and sponsor queries in a timely manner.

· Perform some phlebotomy

· Perform Quality Control (QC) checks on all trials per company SOP and interface with QA Director as needed

Recruitment Responsibilities

· Provide weekly updates to Active Studies Report

· Communicate all advertising needs to recruitment team

· Maintain weekly communication with recruitment team to maximize recruitment in all enrolling trials

Minimum Qualifications:

  • At least 2 yrs of experience as a CRC in clinical research or relevant clinical role
  • CCRC or CCRP certification preferred

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Report to duty at physical locations other than the primary assigned location(s) on an as-needed basis. The fluctuating nature of the industry and the existence of multiple physical business addresses mean that employees must be prepared to adjust work location within reason as dictated by business needs.

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