Research Assistant

About Company:

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.This role will assist the clinical teams with calling subjects, follow up with documents, assist on the phase 1 unit as needed.

Responsibilities:

• Prepare source documents for study visits.
• Perform vitals, ECGs, and phlebotomy.
• Data Entry from patient visit
• Manage lab kit inventory.
• 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 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 degree preferred.
• Requirements
  • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Knowledgeable in medical terminology
  • Organization skills required.
  • Good organizational and interpersonal skills
  • Attention to detail.
  • Excellent communication skills (interpersonal, written, verbal)