Clinical Research Assistant

Accel Research Sites

Birmingham (AL)

On-site

USD 36,000 - 48,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental, vision
Life insurance
401k with match
HSA

Job summary

Accel Research Sites in Birmingham, AL is seeking a Clinical Research Assistant/Medical Assistant to support CRCs, Site Manager, and investigators in accordance with GCP, ICH, HIPAA and FDA SOPs. The RA performs clinical, lab and administrative tasks to help the site run smoothly.

You will assist with patient screening, follow-up visits, data entry in EDC, obtain vital signs and possibly blood draws, manage logs and charts, and coordinate study visits.

Qualifications

  • High School diploma and 1 year admin/clinical experience required.
  • 1 year or more clinical research or clinical experience preferred.
  • Bi-lingual (English/Spanish) proficiency a plus.
  • Proficiency with MS Office, email, EHRs, web apps; typing 40+ wpm.
  • Strong organizational, written and verbal communication skills.
  • Interpersonal skills; ability to work independently and with others.
  • Ability to manage multiple tasks and adapt to changing workloads.
  • Demonstrates integrity and dependability; HIPAA compliant.

Responsibilities

  • Assist CRCs, Site Manager and investigators by performing duties per study protocol.
  • Screen patients for enrollment and schedule visits; assist with follow-ups.
  • Document in source charts; enter data in EDC; respond to data queries.
  • Obtain vital signs and ECGs; may perform blood draws and basic lab procedures.
  • Maintain study logs, charts and filing; coordinate patient visits and reminders.
  • Ensure confidentiality of patient and company information per HIPAA.

Skills

Administrative skills
Clinical assistance
HIPAA compliance
Bilingual English/Spanish
Data entry
Communication
Attention to detail
Time management

Education

High School diploma

Tools

Microsoft Office
Electronic health records
EDC

Job description

Clinical Research Assistant/ Medical Assistant

Department: Operations

Employment Type: Full Time

Location: Accel Research Sites - Birmingham, AL

Reporting To: Jessica Fellows

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.
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