What You'll Do
Lead monitoring activities for clinical trials using both on-site and remote methods to uphold standards in data quality, regulatory compliance, and protocol adherence. You will play a key role in maintaining the integrity of clinical study execution across international sites.
Develop standardized tools such as monitoring checklists, reporting templates, and quality procedures to enhance consistency and efficiency. Support the design and refinement of clinical protocols and contribute to the implementation of best practices in trial management.
Supervise and mentor junior team members, providing training on monitoring techniques and regulatory expectations. Oversee daily site operations, ensuring accurate documentation, timely reporting, and resolution of data discrepancies. Collaborate with data management, biostatistics, and regulatory teams to support end-to-end trial delivery.
Identify and resolve issues affecting trial conduct or data validity, applying strong analytical skills to maintain compliance with Good Clinical Practice (GCP) and applicable regulations. Prepare detailed monitoring reports and support submissions to regulatory authorities.
Requirements
Hold a bachelor’s degree in a relevant discipline and bring at least 3–5 years of experience in clinical research or a closely related field. Demonstrate solid understanding of clinical trial workflows, GCP guidelines, and regulatory standards.
- Proven ability to manage multiple priorities with precision and organization
- Strong problem-solving capabilities and attention to detail
- Excellent written and verbal communication skills
- Proficiency with clinical trial management systems and related software
- Ability to work independently and collaboratively within cross-functional teams
Preferred Qualifications
- Certified Clinical Research Professional (CCRP) or equivalent credential
Benefits
Access structured career development paths and ongoing training in therapeutic and technical domains. Work in an environment that values authenticity, diverse perspectives, and professional growth.
Receive support through comprehensive resources, peer recognition programs, and a culture that encourages initiative and inclusion. Gain exposure to emerging science and technologies while collaborating with industry experts.
Be part of a team focused on advancing therapies efficiently and meaningfully, with integration into customer success frameworks and functional specialty groups.
