Field Clinical Research Associate At Denver Co Jobs in Maryland , Employment

Are you looking for an exciting opportunity to join a leading clinical research team in Denver, CO? We are seeking a Field Clinical Research Associate to join our team and help us develop innovative treatments for patients. In this role, you will be responsible for conducting on-site clinical research activities, including patient recruitment, data collection, and monitoring of clinical trials. If you have a passion for clinical research and are looking for a challenging and rewarding career, this could be the perfect opportunity for you!

Overview A Field Clinical Research Associate (FCRA) at Denver Co is responsible for providing clinical research support to the company’s clinical research studies. This position requires the FCRA to travel to various sites to conduct clinical research activities, such as patient recruitment, data collection, and study monitoring. The FCRA must ensure that all research activities are conducted in accordance with applicable regulations and guidelines. Detailed Job Description

The Field Clinical Research Associate (FCRA) at Denver Co is responsible for providing clinical research support to the company’s clinical research studies. This position requires the FCRA to travel to various sites to conduct clinical research activities, such as patient recruitment, data collection, and study monitoring. The FCRA must ensure that all research activities are conducted in accordance with applicable regulations and guidelines. The FCRA will be responsible for the following duties:

• Developing and maintaining relationships with clinical research sites

• Coordinating and conducting patient recruitment activities

• Collecting and entering data into the company’s clinical research database

• Monitoring clinical research studies to ensure compliance with applicable regulations and guidelines

• Assisting with the preparation of regulatory documents

• Assisting with the preparation of study reports

• Assisting with the development of study protocols

• Assisting with the development of study budgets

• Assisting with the development of study materials

• Assisting with the development of study timelines

• Assisting with the development of study procedures

• Assisting with the development of study training materials

• Assisting with the development of study monitoring plans

• Assisting with the development of study closure plans

Job Skills Required

• Knowledge of clinical research regulations and guidelines

• Knowledge of clinical research databases

• Knowledge of clinical research processes and procedures

• Knowledge of patient recruitment techniques

• Knowledge of data collection and entry techniques

• Knowledge of study monitoring techniques

• Knowledge of regulatory document preparation

• Knowledge of study report preparation

• Knowledge of study protocol development

• Knowledge of study budget development

• Knowledge of study material development

• Knowledge of study timeline development

• Knowledge of study procedure development

• Knowledge of study training material development

• Knowledge of study monitoring plan development

• Knowledge of study closure plan development

• Excellent communication and interpersonal skills

• Excellent organizational and time management skills

• Ability to work independently and as part of a team

• Ability to travel to various sites

Job Qualifications