Clinical Data Monitor, Phase I - Dallas, TX

FortreaDallas, TX
16hOnsite

About The Position

As one of the largest Clinical Research Organizations globally, we operate Early Phase Clinical Research Units in both the United States and the United Kingdom. We are currently seeking a Clinical Data Monitor to join our Dallas, TX team in a full‑time, office‑based role. The Clinical Data Monitor supports core clinical data management activities by ensuring accuracy, completeness, and regulatory compliance throughout the study lifecycle. This role is key in maintaining study documentation, performing accurate data entry, and assisting with operational tasks across multiple projects. In this position, you will contribute to early‑phase clinical trials that evaluate the safety and pharmacokinetics of investigational drugs. You’ll collaborate with teams conducting studies for leading pharmaceutical, biotechnology, and medical device companies, gaining valuable exposure to new therapies and emerging medical technologies.

Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, or related field preferred
  • Relevant experience may be considered in lieu of degree
  • 1–2 years of experience in a research environment or related setting
  • Strong attention to detail and accuracy
  • Effective communication and organizational skills
  • Ability to work collaboratively within a team
  • Experience in clinical research is a plus

Nice To Haves

  • Experience coordinating people or processes; customer‑service experience helpful.

Responsibilities

  • Follow project guidelines for scanning, indexing, data entry, tracking, and administrative tasks
  • Scan, index, and manage study documents, including CRFs and essential records
  • Enter and verify clinical data with high accuracy
  • Assist with EDC account setup, updates, and deactivations
  • Support decommissioning activities (PDF/media QC, shipment prep, and tracking)
  • Maintain project files in eTMF/TMF per SOPs, GCP, and ICH requirements
  • Perform archiving duties for paper and electronic records
  • Complete additional tasks as needed to support study operations

Benefits

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO)
  • Employee recognition awards
  • Multiple ERG’s (employee resource groups)
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