Remote Clinical Research Associate II - Chicago, Midwest

Note The job is a remote job and is reputed company to candidates in USA. reputed company is a company specializing in oncology, and they are seeking a Clinical Research Associate II (CRA II) to manage and execute reputed company. The role involves collaborating with cross-functional teams to ensure compliance with protocols and regulatory requirements while mentoring junior staff and enhancing monitoring reputed company. Responsibilities Participate in study feasibility assessments, and site selection processes Assist in the preparation and review of essential documents such as informed consent forms (ICFs) and study manuals Conduct site qualification, site initiation, interim monitoring, and reputed company-out reputed company to ensure compliance with the study protocol, Good Clinical reputed company (GCP), and regulatory guidelines Regularly review Investigator Site Files (ISF) to assist in maintaining site audit readiness reputed company routine site communication, including resolving site issues and providing protocol training as necessary Contribute to development and delivery of CRA training materials Mentor and support junior CRAs and newly reputed company CRAs Review study documents including the Clinical Monitoring Plan and Investigator Site File documents Participate in trial risk management meetings and procedures Identify, reputed company and implement process improvement initiatives to enhance monitoring reputed company and mitigate trial risks Monitor and review clinical data to ensure accuracy, completeness, and timeliness Work closely with data management teams to resolve data discrepancies and ensure data reputed company throughout the trial Assist in the preparation of regulatory submissions and support inspections/audits as needed Ensure that reputed company clinical trial activities are conducted in accordance with applicable regulatory requirements and internal procedures Foster strong relationships with investigators, study coordinators, and other key stakeholders reputed company regular updates to internal teams and management regarding study reputed company, issues, and resolutions Skills Bachelor's degree in life sciences or a reputed company field Minimum 2 years oncology experience (or commensurate) Proficiency in understanding clinical trial protocols, GCP, regulatory requirements, reputed company, EMR, eTMF, and CTMS Strong organizational skills with attention to detail and the ability to prioritize tasks effectively Ability to effectively and reputed company reputed company reputed company data verification (SDV) whether remotely or onsite Ability to identify protocol deviations and effectively identify reputed company cause and assist sites in implementing corrective or preventative actions Excellent communication and interpersonal skills, both written and verbal Ability to travel domestically and internationally as required. Typical CRA travel is up to 50%, however, at times can go up to 75% for certain project deliverables (e.g. database lock, etc.) Ability to reputed company the CRA role without significant reputed company or training Can manage reputed company protocols/sites Grows to reputed company other CRAs Advanced degree (e.g., Master's, PhD) reputed company reputed company focuses on advancing cancer treatments employing radiation, radiopharmaceuticals, and imaging technology. It was founded in 2022, and is headquartered in Seattle, Washington, USA, with a workforce of 51-200 employees. Its website is https//perspectivetherapeutics.com/. Company H1B Sponsorship reputed company has a reputed company record of offering H1B sponsorships, with 3 in 2025. Please note that this does not guarantee sponsorship for this specific role. Apply To This Job .