Research Assistant (RA)-FT at Evolution Research Group

Columbus, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Sep, 26

Salary

0.0

Posted On

07 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Collection, Data Analysis, Phlebotomy, ECG Performance, Vitals Monitoring, Specimen Processing, Regulatory Compliance, Medical Terminology, Clinical Documentation, Inventory Management

Industry

Research Services

Description

About Us: 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. We are seeking a highly motivated PRN Research Assistant (RA) to join our team. You will be responsible for assisting with research studies, collecting and analyzing data, and ensuring compliance with study protocols. 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: * Assist with research studies by collecting and analyzing data * Ensure compliance with study protocols and regulations * Maintain accurate and complete records of research activities * 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. Minimum Qualifications: * High School Diploma or its equivalent; College degree preferred. * 1 year of clinical experience is preferred. * Strong organizational and communication skills * Ability to work independently and as part of a team * Attention to detail and accuracy Preferred Qualifications: * Experience with clinical research studies * Knowledge of regulatory requirements for research studies * Knowledgeable in medical terminology

Responsibilities

The Research Assistant is responsible for collecting and analyzing study data while ensuring strict compliance with protocols and FDA regulations. Key tasks include performing clinical procedures like phlebotomy and ECGs, managing lab inventory, and maintaining accurate research records.