Research Assistant

Evolution Research Group; Miami (FL); On-site; USD 24,796 - 33,062; Full time

Benefits offered by this job

Medical and dental coverage

Matching 401(k)

Paid time off

Job summary

Evolution ResearchGroup in Miami, FL, is seeking a Research Assistant to support clinical trial activities under FDA, GCP, and ICH guidelines. This full-time role involves preparing source documents for study visits, performing vitals and phlebotomy, and data entry to ensure accurate patient data and compliant workflows.

The ideal candidate will have strong organizational and communication skills, attention to detail, and a willingness to work night shifts in a fast-paced research environment.

Qualifications

• 1 year of clinical experience is preferred.
• High School Diploma or equivalent; College degree preferred.
• Understand regulatory requirements, GCP and ICH guidelines.
• Knowledgeable in medical terminology.
• Strong organizational and interpersonal skills.
• Excellent communication skills (written and verbal).
• 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.
• May include additional responsibilities as required by ERG.

Skills

Communication

Organization

Attention to detail

Interpersonal skills

Medical terminology

Regulatory knowledge (GCP/ICH)

Night shift

Education

High School Diploma or equivalent

College degree preferred

1 year of clinical experience

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

Full Time CPMI-Clinical Pharmacology Miami, Miami, FL, US

2 days ago Requisition ID: 1438

Salary Range: $18.00 To $24.00 Hourly

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