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Alcanza Clinical Research logo

Research Assistant

Alcanza Clinical Research·Vestavia Hills, Alabama

Full Time·On Site·0-2 yrs·Posted 18 days ago
Practice for this role

About the role

The Research Assistant supports clinical research coordinators and investigators by performing clinical, lab, and administrative tasks. Key duties include patient screening, collecting vital signs, performing blood draws, and managing study data in EDC systems.

Research Assistant Department

  • Operations
  • Employment
  • Type:
  • Full
  • Time
  • Location:
  • Accel
  • Research
  • Sites -
  • Birmingham,
  • AL
  • Reporting To: Adrienne Hilliard

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.

Key Responsibilities Essential Job Duties

  • In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed.
  • Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws;
  • Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner. Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed; Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and Perform all other duties as requested or assigned.

Skills, Knowledge and Expertise

Minimum Qualifications

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.

Required Skills

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.

Benefits

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.

Requirements

A high school diploma and one year of administrative or clinical experience are required. Proficiency in Microsoft applications and strong organizational skills are essential, while clinical research experience and bilingual proficiency in Spanish are preferred.

  • high school
  • Written Communication
  • Verbal Communication
  • HIPAA Compliance
  • Phlebotomy
  • Electronic Health Records
  • Microsoft Office
  • Data Entry
  • Clinical Research
  • GCP
  • Patient Scheduling
  • Lab Procedures
  • Patient Screening
  • FDA Regulations
  • ICH Guidelines
  • Medical Record Tracking
  • ECG Operation

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Vestavia Hills, Alabama
Posted
Jul 9, 2026
Application
Employer website
Alcanza Clinical Research logo

Hiring organization

Alcanza Clinical Research

At Alcanza℠, we believe in the power of clinical research to move healthcare forward for all patients. Because research is the first step in bringing approved treatments to market, we encourage everyone to learn more about participating.

IndustryResearch Services
TypePrivately Held
Size201-500 employees
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Market context

Operations roles in Alabama labs

Operations roles in Alabama healthcare settings often stay tied to steady lab and clinical workflow needs, especially where facilities rely on trained staff to keep testing and reporting moving. These jobs can be competitive because employers look for candidates with a relevant science degree, ASCP-approved clinical training, and preferred ASCP registration, plus practical laboratory technology competency. Review the AI-summarized requirements and benefits on this platform, then compare your training against the ASCP and lab-tech expectations before applying.

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