Clinical Research Assistant
Alcanza Clinical Research·Woodstock, New York
Alcanza Clinical Research·Woodstock, New York
Provides clinical, lab, and administrative support to the research team to ensure the successful operation of clinical trials. Key duties include patient screening, collecting vital signs, performing lab procedures, and maintaining study documentation in compliance with regulations.
Description Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.
Skills, Knowledge and Expertise
A High School diploma and 1 year of administrative / clinical experience is required. 1 year or more years of clinical research or clinical experience is preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm). Must possess strong organizational skills and attention to detail. Well-developed written and verbal communication skills. Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers. Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. Must be professional, respectful of others, self-motivated, and have a strong work ethic. Must possess a high degree of integrity and dependability. Ability to work under minimal supervision, identify problems and implement solutions. Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
Requires a high school diploma and at least one year of administrative or clinical experience. Proficiency in computer applications and strong organizational and communication skills are essential.
Market context
Clinical Research Assistant roles in New York are often competitive because employers look for hands-on patient-facing experience plus research compliance knowledge. This posting is especially selective with phlebotomy proficiency, Spanish bilingualism, and familiarity with GCP and FDA regulations, so candidates should match their experience closely and highlight any clinical documentation or specimen-collection work. Job requirements and benefits on this platform are AI-summarized from the original job description, saving you research time.
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