Clinical Research Associate in United States at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Research Associate in United States.

This role plays a key part in advancing ophthalmic clinical research by ensuring the successful execution, quality, and compliance of clinical trials across multiple study sites. You will build and maintain strong relationships with investigators and site teams while overseeing study conduct in alignment with ICH-GCP guidelines, regulatory requirements, and study protocols. Working within a collaborative and science-driven environment, you will contribute to the development of innovative ophthalmic therapies that aim to improve patient outcomes globally. The role combines field-based monitoring with cross-functional coordination, offering exposure to all phases of clinical trial execution. You will also help ensure data integrity, patient safety, and operational excellence throughout the study lifecycle. This is an impactful opportunity to contribute directly to advancing vision science and global healthcare innovation.

• Conduct remote and on-site monitoring visits (initiation, interim, evaluation, and close-out) to ensure compliance with study protocols and regulatory standards
• Develop and maintain strong relationships with clinical sites, ensuring consistent communication and operational alignment throughout trials
• Review and verify clinical data to ensure accuracy, completeness, and adherence to Good Clinical Practice (GCP) guidelines
• Support site selection, feasibility assessments, and study start-up activities in coordination with internal teams
• Collect, review, and manage essential regulatory and study documentation across CTMS, eTMF, and related systems
• Identify, assess, and escalate site performance, compliance, or quality issues as needed
• Collaborate with investigators and site staff to address protocol deviations, recruitment challenges, and study-related inquiries
• Ensure timely and accurate reporting of monitoring findings and study visit documentation

• Bachelor’s degree with at least 2 years of Clinical Research Associate experience or equivalent combination of education and experience
• Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and site monitoring practices
• Experience in clinical site monitoring, including source data verification and regulatory documentation review
• Ability to interpret clinical protocols and ensure adherence to study requirements
• Strong attention to detail with excellent organizational and documentation skills
• Proficiency with clinical systems such as CTMS and EDC, as well as Microsoft Excel
• Strong communication and interpersonal skills with the ability to build effective site relationships
• Ability to manage multiple site visits and prioritize tasks in a fast-paced environment
• Ophthalmology clinical research experience is highly preferred
• Multilingual abilities are considered a plus

• Competitive salary aligned with experience and market standards
• Comprehensive medical, dental, and vision insurance starting from day one
• Flexible PTO policy with unlimited sick time and paid company holidays
• 401(k) retirement plan with employer matching contributions
• Paid parental leave, fertility support, and adoption assistance
• Life and disability insurance fully covered by the employer
• Remote work support and wellness reimbursement programs
• Career development opportunities within a global clinical research environment
• Inclusive, mission-driven culture focused on scientific innovation and patient impact