Clinical Research Associate II

As a Clinical Research Associate II, you will contribute to the successful delivery of clinical trials across a range of therapeutic indications. You will conduct on-site monitoring activities, support study startup, and help ensure that clinical research is performed in accordance with established quality standards. Working closely with clinical sites, investigators, internal project teams, vendors, and regulatory specialists, you will help maintain effective communication and study progress. Your responsibilities will span monitoring visits, source document verification, clinical data review, and query resolution. You will also support feasibility activities and the preparation of regulatory submission documentation. This opportunity offers exposure to different therapeutic areas, allowing you to strengthen your clinical research expertise and continue developing your career in a quality-focused international environment.

• Conduct and document all types of on-site clinical monitoring visits, ensuring study activities meet applicable quality standards and requirements.

• Participate in study startup activities and feasibility research to support effective site selection and study preparation.

• Perform Case Report Form (CRF) reviews, source document verification, and clinical data query resolution.

• Manage site communications and relationships, maintaining effective coordination with investigators and site personnel.

• Serve as a point of contact for internal support services and external vendors, helping address study-related needs.

• Communicate regularly with internal project teams regarding site activities, study progress, and relevant issues.

• Collaborate with regulatory teams to prepare and gather documentation required for clinical study submissions.

• Support the consistent and timely execution of clinical research activities across assigned studies and therapeutic indications.

• College or university degree in Life Sciences, or an equivalent combination of education, training, and professional experience.

• Independent on-site clinical monitoring experience in Argentina, as specified in the original posting.

• Experience conducting all types of monitoring visits for Phase II and/or Phase III clinical trials.

• Full professional working proficiency in both English and Spanish.

• Proficiency in Microsoft Office applications.

• Strong planning and organizational skills, with the ability to manage responsibilities in a dynamic team environment.

• Effective communication and collaboration skills, with the ability to work with clinical sites, internal teams, and external partners.

• Strong analytical thinking and problem-solving abilities.

• Willingness and availability to travel as required by clinical study activities.

• Experience in oncology is preferred.