Clinical Trial Assistant

Overview

Support study start-up, maintenance, and close-out for clinical trials.

Key Responsibilities

• data collection
• query resolution
• document development
• study start-up
• regulatory prep
• supply management

Tasks

-Support data collection and query resolution. -Assist in the development and review of study-related documents (e.g., protocols, ICFs, CRFs, monitoring plans). -Support study start-up, maintenance, and close-out activities across multiple clinical trials. -Assist in the preparation of regulatory documents, ethics committee applications, and study start-up materials as needed. -Track and manage clinical supplies, shipments, and site communications. -Coordinate with CROs, clinical sites, and vendors to ensure timely delivery of study milestones. -Participate in internal and external meetings, including meeting minutes and following up on action items.

Requirements

• bachelor's
• cta experience
• ivdr
• excel
• clinical utility
• post‑market

What You Bring

-Bachelor’s degree in life sciences, healthcare or related field. -3–5 years of experience as a CTA in biotech, diagnostics, or medical device industry. -Knowledge of clinical utility and performance evaluation studies. -Prior involvement in post-market surveillance activities. -Experience supporting Class C IVD studies under IVDR. -Proficient Excel, Word and PowerPoint skills.

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Benefits

-Employee Assistance Program -Short and long-term disability -Time Off/Leave (PTO, Vacation or Sick Leave) -Medical, dental & vision -Life Insurance (Voluntary Life & AD&D for the employee and dependents) -Critical Illness, Accident, and Hospital -Health Spending Account (HSA) -Transportation benefits -401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available

About Actalent

-Born in July 2021 by merging Aerotek’s engineering & sciences arm with EASi, Actalent emerged as a focused engineering-and-science partner. -Backed by Allegis Group, it drives scale and speed to market via contract, managed, and technical services. -Headquartered in Maryland with global reach, it deploys specialized teams across North America, Europe, and APAC on Fortune 500 projects. -Typical engagements span EV design, vaccine development, lab services, clinical research, and infrastructure systems. -Expertise covers a wide spectrum: aerospace, defense, healthcare, manufacturing, software systems, environmental and civil engineering.

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