Research Assistant (PRN, 11p-7a)

Evolution Research Group; Miami (FL); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

401(k) match

Paid time off

Job summary

Evolution Research Group in Miami is seeking a Research Assistant to help ensure protocol compliance and support clinical objectives across FDA-regulated trials. You will assist with source document preparation, vitals, ECGs, phlebotomy, and data entry, while processing specimens and completing protocol trainings.

The role requires knowledge of GCP and ICH guidelines, strong medical terminology, excellent communication and organizational skills, and willingness to work a NIGHT SHIFT.

Qualifications

• Regulatory requirements, GCP and ICH guidelines.
• Knowledgeable in medical terminology
• Organization skills required.
• Good organizational and interpersonal skills
• Attention to detail.
• Excellent communication skills (interpersonal, written, verbal)
• Must be willing to work a NIGHT SHIFT

Responsibilities

• Prepare source documents for study visits.
• Perform vitals, ECGs, and phlebotomy.
• Data Entry from patient visit
• Ship and process specimens
• Undertake protocol trainings as assigned.
• General office tasks such as filing, copying, and scanning.
• Additional duties as required by ERG

Skills

Regulatory knowledge

GCP/ICH knowledge

Medical terminology

Organizational skills

Attention to detail

Communication skills

Night shift willingness

Education

High School Diploma

College degree

Job description

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

• Prepare source documents for studyvisits.
• Perform vitals, ECGs, andphlebotomy.
• Data Entry from patient visit
• Ship and process specimens
• Undertake protocol trainings as assigned.
• General office tasks such as filing, copying, andscanning.
• Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

• Education and experience
  • 1 year of clinical experience is preferred.
  • High School Diploma or its equivalent; College degreepreferred.
• Requirements
  • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Knowledgeable in medical terminology
  • Organization skillsrequired.
  • Good organizational and interpersonal skills
  • Attention to detail.
  • Excellent communication skills (interpersonal, written, verbal)
  • Must be willing to work a NIGHT SHIFT