Description
Our FSP team is currently seeking a CRA 2 with 2 years of monitoring experience. This is a hybrid role requiring 8-10 days on site per month, primarily in the Las Vegas, NV area, with a focus on Oncology.
You will utilise your skills, knowledge, and clinical judgement to provide high-quality care for participants in clinical trials and respond to emergency situations based on clinical research standards.
Responsibilities:
- Manage all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.
- Liaise with vendors and perform other duties as assigned.
- Ensure study staff receive proper materials and instructions to safely enter patients into the study.
- Verify that informed consent procedures and protocol requirements are adhered to according to regulatory requirements.
- Protect the integrity of data submitted on Case Report Forms (CRFs) or other data collection tools.
- Perform CRF review, query generation, and resolution against established data review guidelines.
- Assist with training new employees and coordinate designated clinical projects as a Local Project Coordinator.
Requirements:
- University or college degree, or certification in a related allied health profession.
- 2 years of Clinical Monitoring experience.
- Ability to work in a fast-paced environment with changing priorities.
- Strong teamwork and people skills.
- Proficiency with technology-based data collection.
Work Environment:
- Office environment with exposure to electrical office equipment.
- Frequent travel to clients/site locations, including occasional domestic and international travel.
Physical Requirements:
- Ability to sit for extended periods and operate a vehicle safely.
- Repetitive hand movement and ability to make fast, simple, repeated movements.
- Occasional crouching, stooping, bending, and twisting.
- Light to moderate lifting and carrying.
Salary: $100-112K per year