Research Assistant
Delray Beach, Florida, United States · Jornada completa
Sé el primero en postularte
- Experiencia
- Más de 1 año
- Salario
- —
- Vacantes
- 1
- Al corriente
- Hace 7 horas
- Modo de trabajo
- En la oficina
- Educación
- High School Diploma or equivalent; college degree preferred
- Reanudar
- Se requiere solicitud
Dónde trabajarás
Descripción del trabajo
About Evolution Research Group
Established in 2014, Evolution Research Group (ERG) specializes in Phase I–IV clinical trial management, focusing on expediting the availability of vital therapies. ERG has established itself as a key player in neuroscience clinical development with affiliate centers nationwide, and experience across clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. Having executed over 5,000 clinical trials, ERG is actively expanding into critical therapeutic sectors in the U.S. and internationally.
ERG fosters a collaborative and supportive environment, offers impactful work opportunities alongside industry experts, and provides comprehensive benefits including medical and dental insurance, a 401(k) with employer matching, and paid leave for rest and recovery.
Role Overview
The Research Assistant will uphold protocol adherence and support the study's overall clinical targets, complying with FDA regulations, Good Clinical Practice (GCP), and ERG’s internal procedures and policies.
Key Responsibilities
- Prepare source documentation for study sessions.
- Conduct vital sign assessments, ECGs, and blood draws.
- Enter data from patient visits accurately.
- Maintain laboratory kit inventories.
- Manage shipment and processing of biological specimens.
- Complete assigned protocol training programs.
- Handle routine office duties such as filing, copying, and scanning.
- Perform additional duties as required by the organization's changing needs, within the scope of ERG’s mandate.
Qualifications and Skills
- Preferred: Minimum one year of clinical experience.
- Education requirement: High School Diploma or equivalent; college degree is favored.
- Solid understanding of regulatory standards, including Good Clinical Practices (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Familiarity with medical terminology.
- Strong organizational abilities and meticulous attention to detail.
- Effective interpersonal and communication skills, both written and verbal.
- Availability to work night shifts is mandatory.