Clinical Research Associate II - East Coast

Evestia Clinical • Florida, FL

1d • Hybrid

About The Position

Evestia Clinical is seeking a Clinical Research Associate II to support clinical trials on the East Coast. The role helps protect the rights, safety, and well-being of trial participants and ensures collected clinical data are accurate, complete, and verifiable against source documents and applicable requirements. Depending on experience, the associate may contribute from study start-up and site initiation through routine monitoring, close-out, and study completion. The position is part of a collaborative global clinical research environment focused on quality, compliance, and patient impact.

Requirements

• Degree in life sciences, nursing, pharmacy, or a related field; equivalent education and clinical research experience may be considered.
• Working knowledge of Good Clinical Practice (GCP), clinical trial regulations, and research ethics.
• Understanding of medical terminology, human physiology, and clinical trial processes.
• Strong written, verbal, and presentation skills.
• Proficiency with information technology and clinical trial systems.
• Excellent customer service, communication, and relationship-building skills.
• Flexibility, adaptability, and attention to detail.
• Ability to work effectively both in a team environment and independently as needed.
• Organizational and time management skills, including prioritizing tasks and meeting project timelines.
• Ability to travel nationally and internationally as required.
• Ideally based on the East Coast or within reasonable access to East Coast clinical trial sites.

Nice To Haves

• Previous experience in clinical research, clinical operations, healthcare, or a related field; experience requirements vary by level.
• For experienced CRA candidates, previous independent monitoring experience and ability to perform applicable site visit types.

Responsibilities

• Perform site management and monitoring activities appropriate to experience, including site qualification, initiation, interim monitoring, and close-out visits.
• Participate in clinical trials from development and planning through study closure.
• Ensure assigned sites comply with study protocols, applicable regulations, ICH/GCP, and Evestia Clinical or sponsor SOPs.
• Review source documentation and clinical data for accuracy, completeness, and consistency.
• Monitor participant safety, informed consent processes, investigational product accountability, and protocol compliance.
• Identify, document, escalate, and support resolution of issues, including protocol deviations and data queries.
• Maintain key performance metrics in accordance with company standards, project requirements, and timelines.
• Prepare monitoring reports and other required study documentation accurately and on time.
• Collaborate with Clinical Team Leads, Project Managers, sponsors, investigators, site personnel, and cross-functional project teams.
• Build and maintain effective relationships with clinical research sites and study stakeholders.
• Complete administrative activities, including expense and time reporting, within company guidelines.
• For more experienced candidates, mentor and guide less experienced team members and provide subject matter support.
• Perform other duties as assigned.

Benefits

• Health insurance, 99% employer-paid.
• Dental and vision insurance, 100% employer-paid.
• Short-term and long-term disability coverage, 100% employer-paid.
• Life insurance policy.
• 401(k) retirement plan with a 3% employer contribution.
• Flexible and hybrid work options.
• Unlimited PTO for salaried staff.
• 12 corporate holidays.
• Employee Assistance Program (EAP).
• Wellness program.
• Learning and development stipend that increases with tenure.
• Charitable match program.
• Catered Wednesday lunches in-office.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level