Research Assistant (PRN)

Evolution Research Group; Miami (FL); On-site; USD 24,796 - 30,307; Part time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution ResearchGroup is seeking a PRN Research Assistant in Miami, FL, to support FDA-compliant clinical studies. The role requires adherence to protocol objectives, GCP, and ICH guidelines while contributing to data collection and specimen handling.

The position emphasizes attention to detail, strong communication, and the ability to work a NIGHT SHIFT in a fast-paced clinical research environment.

Qualifications

• 1 year of clinical experience preferred.
• High School Diploma or equivalent; College degree preferred.
• Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
• Knowledgeable in medical terminology.
• Strong organizational and interpersonal skills.
• Attention to detail with excellent communication (written and 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.

Skills

GCP knowledge

ICH guidelines

Medical terminology

Organizational skills

Interpersonal skills

Attention to detail

Written communication

Verbal communication

Night shift willingness

Education

High School Diploma or equivalent

College degree (preferred)

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Research Assistant (PRN)

PRN CPMI-Clinical Pharmacology Miami, Miami, FL, US

2 days ago Requisition ID: 1437

About Company:

Evolution ResearchGroup (ERG) is dedicated to delivering high-quality Phase I–IV clinical trialexecution to help sponsors bring lifesaving and life-enhancing therapies tomarket quickly and safely. Founded in 2014, ERG has grown into a leadingneuroscience 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 andcontinues 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