CRF Specialist I - Part Time / Daytona Beach, FL (On-Site)

Fortrea•Daytona Beach, FL

18h•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 I / Part-Time, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. 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/clinic-based job in Daytona Beach, FL. 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 are drawn to this 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 have a close face-to-face relationship with participants, and as you continue 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
1-2 years experience specific to CRF data and case reporting, industry experience, sponsor experience
Comfortable working in an environment that is fast paced, has changing priorities, is technology based.

Nice To Haves

Clinical Research experience is preferred
Teamwork and people skills are essential for the study to run smoothly.

Responsibilities

Transcribe study data into case report form
Enter data into the computer using the currently defined data management software.
Work in conjunction with study coordinators, quality, and project manager to ensure that case report form completion timelines are met.
Work with sponsors during monitoring visits to ensure all data questions and clarifications are answered.
Timely follow-up and resolution to all sponsor generated data queries
Constantly look for ways to improve the efficiency and quality of unit work processes.
Perform other related duties as assigned.