Research Assistant

Evolution Research Group; Columbus (OH); On-site; USD 26,174 - 31,684; Full time

Benefits offered by this job

Medical insurance

Dental insurance

401(k) matching

Paid time off

Job summary

Evolution Research Group in Columbus, OH is seeking a Research Assistant to support clinical trial activities, ensuring adherence to protocol, FDA regulations, Good Clinical Practice (GCP), and SOPs. You will manage source documents, collect vitals, perform ECGs and phlebotomy, and handle data entry and specimen processing.

This PRN role may include night shifts and routine office tasks; a high school diploma is required (college degree preferred), with strong organizational, communication, and

Qualifications

• Understand regulatory requirements and GCP/ICH guidelines.
• Knowledgeable in medical terminology and clinical terminology.
• Excellent written and verbal communication skills; strong organizational ability.

Responsibilities

• Prepare source documents for study visits.
• Perform vitals, ECGs, and phlebotomy.
• Data entry from patient visits.
• Ship and process specimens.
• Undertake protocol trainings as assigned.
• General office tasks such as filing, copying, and scanning.
• Role may expand to meet ERG objectives.

Skills

Regulatory knowledge

GCP/ICH familiarity

Medical terminology

Organization skills

Interpersonal communication

Attention to detail

Night shift willingness

Excellent communication

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 Columbus, OH, US

3 days ago Requisition ID: 1433

Salary Range: $19.00 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