Role: Clinical Research Associate II specializing in Oncology monitoring.

Responsibilities Conduct site qualification, initiation, monitoring, and close-out visits.

Ensure protocol adherence, data integrity, and patient safety.

Collaborate with investigators and site staff to facilitate study progress.

Perform data review and resolve queries to maintain high-quality data.

Assist in preparing and reviewing study documentation, including protocols and reports.

Qualifications & Skills Bachelor's degree in a scientific or healthcare field.

At least 2 years of clinical trial monitoring experience, specifically in Oncology.

Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Strong organizational, communication, and attention to detail.

Ability to work independently and as part of a team.

Willingness to travel (~60%).

Additional Info: The role offers competitive compensation, health benefits, retirement plans, and opportunities for professional development. The organization values diversity, inclusion, and accessibility in the workplace.