Clinical Trials Coordinator

Arkana LaboratoriesLittle Rock, AR
1dOnsite

About The Position

As the Clinical Trials Coordinator is an entry-level role that supports a team of coordinators and technical staff in delivering renal pathology services for clinical trials. Reporting directly to the Clinical Trials Specialist Lead, this position is vital to the daily operations of the Clinical Trials Department and works collaboratively across all Arkana departments. Key responsibilities include: Ensuring accurate chain-of-custody for samples Accessioning and processing samples Slide scanning and document management Performing other tasks as assigned by the department lead to ensure seamless departmental function This role offers a pathway to a career in histopathology and/or client services, encouraging growth into specialized technical, client-facing, or leadership roles. The selected candidate will play a critical part in the team’s success and is expected to attain Good Clinical Laboratory Practice (GCLP) certification.

Requirements

  • Education: Associate or bachelor’s degree
  • Experience: No experience is required. Candidates with work experience and up to three (3) positive references will receive preference
  • Computer Skills: Proficient in Microsoft Office and ability to gain proficiency in specialized inventory management software.
  • Ability to read, write, and speak English is required.
  • Ability to develop proficiency in medical terminology is required
  • Schedule: Monday-Friday 8am-5pm, onsite at the main office in Little Rock, AR. This is an onsite position at our main office in Little Rock, Arkansas, applicants must live within 1 hour drive of the main office in Little Rock.

Responsibilities

  • Collaborate with the CT Specialist Lead to support the Department in daily operations
  • Receive and accession Clinical Trials' samples using specialized software
  • Conduct archiving duties including scanning documents
  • Participate in the management of a de-identified clinical trials digital archive
  • Assist in the creation of forms (e.g. trial-specific scoring forms and related documentation)
  • Follow trial-specific instructions to assist with the upload of time-sensitive materials
  • Ensure delivery of samples within departments at Arkana
  • Deliver slides to specific departments or pathologists as needed
  • Assist other Clinical Trials Coordinators with all duties related to daily clinical trials operations
  • Complete subject tracking and document management
  • Assist with the return materials to clinical trials sponsors
  • Provide administrative support as needed to maintain daily operations within the Clinical Trials Department
  • Other duties as assigned

Benefits

  • Competitive salary
  • Generous paid time off and Paid Holidays
  • Minimal cost health insurance for you and affordable options for your family
  • 401(k) with immediate eligibility and match
  • Company-paid life insurance
  • Company-paid long term disability coverage
  • Affordable vision and dental plans
  • Flexible Spending Account or Health Savings Account availability
  • Wellness plan and complimentary yoga classes
  • Monthly in-office massages and employer-sponsored lunches
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service