CRF Specialist, Early Phase Clinical Research- Dallas, TX

Fortrea•Dallas, TX

1d•Onsite

About The Position

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a CRF Specialist, to be responsible for transcribing and managing study data, ensuring accuracy, and collaborating with various stakeholders to meet project timelines and quality standards. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.) This is a full-time, office-based position in Dallas, TX. If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug. Many Specialists are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.

Requirements

High school diploma or equivalent. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
1-2 years’ experience in a research environment or related experience.
Strong attention to detail and accuracy.
Excellent communication and organizational skills.
Ability to work collaboratively with a team.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Nice To Haves

Experience in clinical research or related field is a plus.
Experience coordinating people or processes; customer‑service experience helpful.

Responsibilities

Transcribe and enter study data into case report forms using Metadata.
Collaborate with quality control and project management teams to ensure timely completion.
Address data questions and classifications during sponsor monitoring visits.
Resolve sponsor-generated data queries promptly.
Communicate effectively with data managers and CRAs, adhering to study protocols and SOPs.
All other duties as needed or assigned.