Clinical Country & Site Associate – Clinical Trial Manager

This is a fully remote position, open to applicants in South Korea.

📋 Description

• Conducts site qualification, site initiation, interim monitoring, site management activities, and close-out visits (either on-site or remotely) to ensure adherence to regulatory standards, ICH-GCP, Good Pharmacoepidemiological Practices (GPP), and protocol compliance.

• Utilizes judgment and experience to assess the overall performance of the site and its staff, providing recommendations for site-specific actions as necessary.

• Maintains an up-to-date understanding of ICH/GCP Guidelines, other relevant regulations, and company SOPs/processes.

• Confirms that the process of obtaining informed consent has been thoroughly executed and documented for each subject/patient.

• Evaluates factors that could impact the safety of subjects/patients and the integrity of clinical data at an investigator/physician site, including protocol deviations/violations and pharmacovigilance concerns.

⛳️ Requirements

• A Bachelor’s degree or RN in a related field, or an equivalent combination of education, training, and experience.

• Familiarity with Good Clinical Practice/ICH Guidelines and other relevant regulatory requirements.

• Strong computer skills and a willingness to adapt to new technologies.

• Outstanding communication, presentation, and interpersonal skills.

• Willingness to manage travel requirements of up to 75% on a regular basis.

🏝️ Benefits

• We are committed to the growth of our employees through career development and progression opportunities.

• Supportive and engaged line management.

• Comprehensive technical and therapeutic area training.

• Peer recognition and a total rewards program.

• An inclusive culture that encourages you to be your authentic self.