Clinical Research Associate- Wound Care

We are seeking a detail-oriented Clinical Research Associate with specialized experience in wound care clinical trials to support the successful execution and oversight of clinical research studies. In this role, you will independently manage site monitoring activities, safeguard data integrity, and ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. You will collaborate with sponsors, investigators, project managers, and cross-functional clinical teams to maintain study quality, address site challenges, and support effective trial delivery. Beyond monitoring, you will contribute to study planning, regulatory documentation, audit readiness, and patient recruitment oversight. You will also help strengthen team performance through mentoring, training, and consistent monitoring practices. This is an opportunity to contribute to meaningful clinical research in a collaborative, international, and innovation-driven environment, with remote work options and opportunities to engage with diverse stakeholders.

• Education: Bachelor's degree in Biology, Life Sciences, or a related scientific discipline.

• Wound care experience: At least 2 years of experience monitoring wound care clinical trials; this is a required qualification.

• Clinical research expertise: Strong knowledge of clinical research practices, ICH GCP, local regulatory requirements, and applicable regulatory and ethical standards.

• Independent monitoring capabilities: Demonstrated ability to manage clinical trial monitoring activities autonomously, prioritize tasks, and ensure quality and compliance throughout the study lifecycle.

• Technical proficiency: Good computer skills and experience using clinical trial management systems, clinical trial databases, and electronic data capture (EDC) platforms.

• Communication and relationship management: Excellent written and verbal communication skills, with the ability to establish and maintain positive working relationships with sponsors, clinical sites, investigators, and project team members.

• Language proficiency: Strong command of the local language, both written and spoken, in the country where monitoring activities are performed. English is also listed as a required language.

• Organization and analytical skills: Strong attention to detail, organizational skills, and the ability to manage multiple tasks in a fast-paced environment while maintaining high standards of accuracy.

• Problem-solving and leadership: Strong analytical, negotiation, meeting management, and cross-functional collaboration skills, along with the ability to resolve complex or ambiguous challenges and provide effective guidance to colleagues.

• Professional approach: Self-motivated, trustworthy, disciplined, adaptable, and comfortable working in a collaborative environment with evolving priorities.

• Travel flexibility: Willingness and ability to travel as needed for onsite monitoring visits and other study-related activities.

• Work location eligibility: The original posting lists remote opportunities in the Americas, including Boston. Candidates based in Brazil should confirm country-specific hiring eligibility and local employment arrangements during the application process.