Research Assistant (PRN, 11p-7a)

Evolution Research Group; Miami (FL); On-site; USD 22,000 - 32,000; Full time

Job summary

Evolution Research Group in Miami, FL, is hiring a Research Assistant (PRN, 11p-7a) to support clinical trial activities under FDA/GCP guidelines. You will prepare source documents, perform vitals/ECGs/phlebotomy, and manage data entry from patient visits with attention to detail.

A high school diploma is required; college degree preferred, with about 1 year of clinical experience. Night shift availability is essential.

Qualifications

• 1 year of clinical experience is preferred.
• High School Diploma or its equivalent; College degree preferred.
• Understand regulatory requirements, GCP and ICH guidelines.
• Knowledgeable in medical terminology.
• Excellent organizational and interpersonal skills.
• Excellent written and verbal communication.
• 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.
• Additionally, this role may encompass responsibilities beyond those outlined, as required by ERG.

Skills

FDA regulations

GCP

ICH guidelines

Medical terminology

Organization skills

Interpersonal skills

Attention to detail

Communication skills

Night shift

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, 11p-7a)

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

Salary Range: $16.00 To $23.00 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