Clinical Research Associate- Wound Care Experience Required

We are seeking an experienced Clinical Research Associate with a strong background in wound care clinical trials to support high-quality clinical research and ensure the successful execution of clinical studies. In this role, you will independently oversee clinical trial site monitoring activities, safeguard data integrity, and ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. You will work closely with sponsors, investigators, project managers, and cross-functional clinical teams to resolve site challenges, support recruitment, and maintain study timelines and quality standards. Your responsibilities will span site qualification, initiation, interim, and close-out visits, as well as regulatory documentation, safety reporting, and audit preparation. You will also contribute to team development by mentoring colleagues, supporting onboarding, and promoting consistent monitoring practices. This opportunity offers the chance to contribute to meaningful healthcare research within a collaborative, international environment that values accountability, innovation, and professional growth.

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

• Wound care monitoring experience: At least 2 years of experience monitoring wound care clinical trials. This is a mandatory requirement for the role.

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

• Independent execution: Proven ability to autonomously manage clinical trial monitoring activities, prioritize responsibilities, and maintain high standards of quality and compliance.

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

• Communication and relationship management: Excellent communication and interpersonal skills, with the ability to build positive, productive relationships with sponsors, clinical sites, investigators, and project teams.

• Language proficiency: English proficiency and a strong command of the local language, both written and spoken, in the country where monitoring activities are performed.

• Organization and attention to detail: Strong organizational skills, meticulous documentation practices, and the ability to manage multiple responsibilities effectively in a fast-paced environment.

• Analytical and problem-solving skills: Ability to analyze complex issues, resolve ambiguous challenges, negotiate solutions, and manage priorities and time effectively.

• Leadership and collaboration: Strong meeting management and cross-functional teamwork skills, with the ability to mentor colleagues, provide constructive guidance, and promote consistency across monitoring teams.

• Professionalism and adaptability: Self-motivated, trustworthy, disciplined, and able to manage stress while maintaining a professional, service-oriented approach.

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

• Location eligibility: The original posting lists remote opportunities in Boston and across the Americas. Candidates based in Brazil should confirm country-specific hiring eligibility, local language requirements, and employment arrangements with the hiring team.