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Assistant Clinical Research Rater Jobs (NOW HIRING)

SRA Trials

Assistant Clinical Research Coord.

Miami, FL

$20 - $30/hr

Assistant Clinical Research Coordinator Suncoast Research Associates is a privately owned and operated research organization established in 2018. We help volunteers get involved in clinical trials ...

Versiti, Inc.

Assistant Clinical Research

Milwaukee, WI · On-site

Position Summary Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...

Versiti, Inc.

Assistant Clinical Research

Milwaukee, WI · On-site

Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...

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How much do assistant clinical research rater jobs pay per hour?

As of May 31, 2026, the average hourly pay for assistant clinical research rater in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What is the difference between Assistant Clinical Research Rater vs Clinical Research Coordinator?

AspectAssistant Clinical Research RaterClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require a bachelor's degreeBachelor's degree in health sciences or related field; certification often preferred
Work EnvironmentRemote or in clinical settings; primarily data review and assessmentsClinical sites; managing study logistics and participant coordination
Employer & Industry UsageResearch organizations, pharmaceutical companies, universitiesHospitals, research institutions, pharmaceutical companies
Common Search & Comparison IntentUnderstanding entry-level roles in clinical researchManaging clinical trials and participant interactions

The Assistant Clinical Research Rater typically focuses on reviewing and assessing data, often working remotely, with minimal direct patient interaction. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including participant recruitment and site management. Both roles are essential in clinical research but differ in responsibilities, required credentials, and work environment.

What cities are hiring for Assistant Clinical Research Rater jobs? Cities with the most Assistant Clinical Research Rater job openings:
What are the most commonly searched types of Clinical Research Rater jobs? The most popular types of Clinical Research Rater jobs are:
What states have the most Assistant Clinical Research Rater jobs? States with the most job openings for Assistant Clinical Research Rater jobs include:
Assistant Clinical Research Rater jobs near you

Assistant Clinical Research Coord.

SRA Trials

Miami, FL

$20 - $30/hr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 4 days ago

Job description

Assistant Clinical Research Coordinator
Suncoast Research Associates is a privately owned and operated research organization established in 2018. We help volunteers get involved in clinical trials which allow patients to play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research. Our company works with all major pharmaceutical companies and conducts studies in a myriad of therapeutic areas. We are located in Doral.
Key Responsibilities
  • Assist in the coordination and support clinical trials from initiation through closeout, ensuring adherence to timelines and study goals.
  • Assist in the development, review, and maintenance of study protocols, standard operating procedures (SOPs), and study-related documents.
  • Serve as a liaison between study sites, investigators, sponsors, and external vendors to ensure effective communication and execution of study activities.
  • Schedule and coordinate participant visits, study procedures, assessments, and data collection activities.
  • Support regulatory submissions by preparing, organizing, and maintaining essential documents in compliance with applicable regulations and guidelines.
  • Assist with participant recruitment, screening, enrollment, and informed consent in accordance with protocol requirements.
  • Perform study-related procedures in strict compliance with approved protocols, GCP guidelines, and regulatory standards.
  • Collect, manage, and accurately enter clinical study data into electronic data capture (EDC) systems.
  • Conduct data quality checks, identify discrepancies, and collaborate with study teams to resolve issues promptly.
  • Maintain accurate, complete, and audit-ready study records and documentation.
  • Monitor study progress and ensure ongoing compliance with protocol, sponsor, and regulatory requirements.
  • Coordinate and support monitoring visits, audits, and inspections.
  • Identify deviations and implement corrective and preventive actions (CAPA) as needed.
  • Collaborate effectively with cross-functional study teams to ensure successful study execution.
  • Participate in sponsor-required training, investigator meetings, and study team calls.
  • Stay current on clinical research regulations, industry guidelines, and best practices.
  • Engage in ongoing professional development and training to enhance clinical research knowledge and skills.
Required Skills and Abilities
  • Bachelor's degree in a relevant field preferred (e.g., life sciences, nursing, public health).
  • Previous experience in clinical research or healthcare preferred.
  • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Strong organizational skills and attention to detail.
  • Excellent communication skills in both English and Spanish and interpersonal skills.
  • Ability to work effectively in a team environment.
  • Proficiency in Microsoft Office and electronic data capture systems.
  • Able to meet our schedule of 7 am to 4 pm.
Benefits:
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance
Schedule:
  • 8 hour shift
  • Monday to Friday

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