Clinical Research Associate (All levels) - North East, USA

Evestia Clinical•Florida, FL

9d•Hybrid

About The Position

Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology. Here, you become a vital part of a global team delivering life-changing impact through clinical excellence. Our foundation is built on principles that define our identity. Innovation drives us to seek new solutions, while Excellence ensures high standards in every project. This is balanced by genuine Care, fostering a supportive culture for both our patients and our people. Above all, we champion Partnership, believing that working together— with trust and flexibility —is the key to our collective success. Our approach is agile and personalized, empowering you to find creative solutions. We offer a welcoming culture that values belonging, ensuring you have the environment needed to thrive and grow. If you are ready to change lives worldwide, join our team. Evestia Clinical is looking Clinical Research Associate (II or Senior), in the North East, to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source.

Requirements

Substantial previous experience independently monitoring and performing all types of site visits
Understanding the principles of Good Clinical Practice (GCP) and clinical trial regulations
Both written and verbal communication and presentation skills
Understanding of medical terminology and human physiology
Proficiency with information technology (computer skills)
Excellent customer service skills
Demonstrated flexibility and adaptability
Ability to work in a team environment and independently as needed
Ability to travel nationally and internationally as required
Organizational and time management skills, able to prioritize tasks and work within timelines

Nice To Haves

Ideally based in the North East

Responsibilities

Performing all and any visit types while ensuring regulatory and protocol compliance
Participate in all aspects of a clinical trial from development and planning to study closure
Comply with applicable regulations, ICH/GCP and Evestia Clinical or sponsor SOPs to assess the safety and efficacy of investigational products (drugs, biologics or devices)
Maintain key performance metrics in accordance with company standards and timelines, ensuring compliance with established monitoring and reporting expectations
Ensure assigned sites are in compliance with the study protocol objectives
Work in project teams and under supervision, reporting to a Clinical Team Lead and/or Project Manager
Liaise effectively between sponsors, investigators and project teams
Completes all administrative tasks (expense and time reporting) within company guidelines
Perform any other duties as assigned