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Location
Remote (Bulgaria)
Visa
Sponsors visas in United States; no register of this country names it
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 11, 2026. Premier Research scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Premier Research is a clinical research organization that runs clinical trials and drug and device development programs for biotech, medtech and specialty pharma companies, headquartered in Morrisville, North Carolina. Its services span full-service clinical research, functional service provider staffing, study design and start-up, monitoring, biostatistics, safety, medical writing and regulatory strategy consulting, with teams across North America, Europe, Latin America and Australia. It hires clinical research associates, clinical leads, project managers, business development directors and regulatory strategy specialists, plus IT security and training staff.
Premier Research is looking for a Associate Data Coordinator to join our Clinical Data Sciences team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

  • Your ideas influence the way we work, and your voice matters here.

  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What You will be Doing:

  • Assists in the preparation of documentation, such as CCGs, DMP, Data Report Specifications, External Data Transfer Specifications, etc.
  • Supports UAT on studies, including testing of edit checks, etc.
  • Assists in maintaining databases and supports DB updates
  • Performs data entry
  • Generates reports for data review
  • Reviews CRFs, data listings to ensure all data captured follow protocol, CCGs, DMP, etc.
  • Generates queries to appropriate internal or external personnel (e.g., investigational sites, Clinical Research Associates and client representatives) to resolve problematic data identified during various aspects of the data management process
  • Reviews responses to queries and resolves discrepancies
  • Assists with external data and/or serious adverse event reconciliation
  • May act as a Lead Data Coordinator or Safety Reviewer
  • Assists document submission to Trial Master File (TMF)
  • Supports TMF Quality Control (QC) activities
  • Supports database QC activities
  • Assists in QC of study reports, CRF archive files
  • Supports the Data Scientist and/or PM in reporting financial project stats, study metrics, dashboard updates, project status

What We Are Looking For:

  • Bachelor’s degree or above (preferably in a Life Science discipline)
  • 0-1 years of industry experience
  • Fluent in English (written and spoken)
  • Strong analytical, investigative, and problem-solving skills
  • Proven ability to learn, navigate, and leverage new systems quickly
  • Exceptional organizational skills, high attention to detail, and a customer-service mindset
  • Ability to multitask and balance competing priorities in a fast-paced environment
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