- Experiência
- Qualquer
- Salário
- —
- Vagas
- 1
- Publicado
- há 2 horas
- Work mode
- No escritório
- Educação
- High School Diploma
- Eligibility
- Candidates with a high school diploma or equivalent can apply. A college degree is preferred. Prior clinical experience is preferred. Applicants must be able to work a night shift.
- Resume
- Required to apply
Where you'll work
Descrição da vaga
About the Company
Evolution Research Group (ERG) focuses on running Phase I through Phase IV clinical trials with an emphasis on safety, speed, and high-quality execution. Established in 2014, the organization has become a major neuroscience clinical development company with affiliated sites across the United States and strong experience in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has supported more than 5,000 trials and is continuing to expand into important therapeutic areas in the U.S. and internationally.
The company highlights a supportive workplace, meaningful day-to-day work, and the chance to contribute to advanced research alongside experienced industry professionals. Benefits mentioned include medical and dental coverage, a matching 401(k), and paid time off.
Role Summary
The Research Assistant supports clinical trial operations by helping maintain protocol compliance and contributing to overall study objectives. This position follows FDA regulations, Good Clinical Practice (GCP), and internal standard operating procedures and policies.
Key Responsibilities
- Prepare source documentation for study visits.
- Carry out vital sign checks, ECGs, and phlebotomy procedures.
- Enter patient visit data accurately.
- Track and maintain lab kit inventory.
- Handle shipment and processing of specimens.
- Complete assigned protocol training sessions.
- Support routine administrative work such as filing, copying, and scanning.
- Take on additional duties as needed to support changing organizational priorities and objectives.
Skills and Qualifications
Applicants should be familiar with regulatory requirements, GCP, and ICH guidelines. The role also calls for understanding of medical terminology, strong organization, attention to detail, and effective communication in interpersonal, written, and verbal forms. Good interpersonal skills are important, and the candidate must be prepared to work a night shift.
Experience in a clinical setting is preferred, and a high school diploma or equivalent is required. A college degree is preferred.
Additional Information
This role is structured as a full-time onsite position in Miami, Florida.
The job description notes that responsibilities may expand or change depending on organizational needs.
Working nights is mandatory for this position.