Research Data Entry/Scheduler (Bilingual)

Arizona Liver Health
Tucson, AZ
On-siteCareer-pivot friendly

Who this role is best for

Geared toward bilingual professionals comfortable with scheduling and data entry in a clinical research setting, with a focus on attention to detail and regulatory compliance in Tucson, AZ.

Best fit for

  • Bilingual individuals with experience in clinical research and strong attention to detail
    — “Bilingual - Spanish speaking required”
  • Candidates with prior experience managing medical records and coordinating appointments
    — “Process/requests medical records for study subjects in a timely manner and presents to Investigator”

Things to consider

  • The role requires handling sensitive medical data and maintaining strict compliance standards
    — “Adhere to IRB approved protocols”
  • Candidates must be prepared for on-site work and some interoffice travel
    — “Some interoffice travel may be required with use of company vehicle or mileage reimbursement”

How to stand out

  • Emphasize prior experience in medical centers or private practices with clinical research
    — “Clinical research experience or experience working in a medical center or private practice”
  • Showcase ability to manage multiple tasks with strong attention to detail and sound judgment
    — “Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail”
  • Demonstrate knowledge of good clinical practice and regulatory compliance in your background
    — “Understand good clinical practice (GCP) and regulatory compliance”
Pace · Fast PacedCollaboration · MediumAutonomy · MediumDecision Impact · Team

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • timely processing of medical records
  • effective communication with research subjects
  • accurate reconciliation of data
Typical background
clinical research experiencemedical center experienceCTMS system experience

Skills & requirements

Required

Clinical ResearchData EntrySchedulingCommunicationProblem-solvingOrganizational SkillsGCP ComplianceCTMS SystemEDC Program

Preferred

Spanish

Stack & domain

CTMS SystemEDC ProgramCommunicationProblem-solvingMulti-taskingOrganizational SkillsClinical ResearchHealthcare

About the role

Original posting from Arizona Liver Health

About Us:

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.

Job Summary:

Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Research Data Entry/Scheduler position in Tucson.  

Title: Research Data Entry/Scheduler (Bilingual) 

Compensation: $19 - $27 per hour, depending on experience

Status: Full-time, Non-exempt

Essential job functions/duties

Reasonable accommodation(s) may be made to enable individuals with disabilities to perform these essential functions.

Process/requests medical records for study subjects in a timely manner and presents to Investigator

Schedule all necessary procedure and research appointments for study subjects

Liaison with vendors to ensure that procedure appointments as well as medical requests are processed in a timely manner

Coordinates on-site monitor visits and responds to requests within 48 hours

Process subject stipends per ICF daily and checks to ensure that stipends have been paid out each month

Communicates with research subjects in a professional manner about stipend of card issues.

Reconcile data daily and monthly on CTMS: unsubmitted visits, unpaid stipends, overdue visits

Audit research trials and filing as needed

Adhere to IRB approved protocols

Comply with institutional policies, standard operating procedures (SOPs) and guidelines

Knowledge/Skills/Abilities Required 

Excellent communication and problem-solving skills

Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail

Understand good clinical practice (GCP) and regulatory compliance

Ability to multi-task.

Excellent organizational skills.

Ability to communicate effectively both orally and in writing.

Relevant subject matter knowledge.

Bilingual - Spanish speaking required

Supervisory responsibilities

None

Work environment

Clinic setting

Physical demands

Able to lift at least 15 lbs.

Able to sit for long periods (at least 50%)

Able to type and do computer work for long periods

Travel Requirements

Some interoffice travel may be required with use of company vehicle or mileage reimbursement

Education, credentials, and/or trainings required

High School Diploma or GED required

Clinical research experience or experience working in a medical center or private practice

Experience using CTMS system and EDC program

Benefits & Perks:

Health, Dental, Vision (with HSA plans and employer contribution)

2 weeks PTO

5 days Sick Time

7 Company Holidays + 2 Company Half-days

401K with company match

Short & Long Term Disability

Educational Assistance

Shared company vehicles for required travel

EEO statement

It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. 

Notice to Staffing Agencies: It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent and pushy inquires may also be blocked across our network as spam. Thank you for your understanding and cooperation.

Source: Arizona Liver Health careers

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