Job Summary
Ctifacts is looking for an experienced Senior Clinical Research Associate to join our team in a remote capacity within the United States. This position demands a candidate with substantial hands-on experience in clinical monitoring and a relevant academic background in nursing or a related field.
Responsibilities
- Oversee and ensure the integrity of clinical trials by monitoring study sites.
- Collaborate closely with research teams to guarantee compliance with protocols and regulations.
- Provide guidance and support to investigators and site staff during study execution.
- Document findings and prepare reports to communicate progress and issues encountered during trials.
- Maintain updated knowledge of clinical research practices and industry standards.
Qualifications
- A minimum of 1 year of experience in on-site clinical monitoring.
- A bachelor’s degree in a relevant field, preferably in nursing or a related discipline.
- Strong analytical and problem-solving abilities.
- Excellent communication skills to work effectively with diverse teams.
- Demonstrated ability to manage time and prioritize tasks in a fast-paced environment.
Ctifacts provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
