Clinical Research Coordinator — Wound Care Trials

SerenaGroup, Inc; Monroeville (Allegheny County); On-site; USD 60,000 - 80,000; Full time

Job summary

SerenaGroup, Inc is seeking a Clinical Research Coordinator in Monroeville to oversee crucial aspects of clinical trials focused on advanced wound care and hyperbaric medicine. You will coordinate trials ensuring compliance, support high-quality patient care, and engage with various stakeholders to meet study goals.

The ideal candidate has a Bachelor’s degree and 1-3 years of relevant experience, with strong organizational skills and proficiency in data management systems. Certifications in clinical research are a plus.

Qualifications

• 1–3 years of experience in clinical research or healthcare setting, preferably in wound care.
• Experience with clinical trial protocols and regulatory requirements.
• Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) preferred.

Responsibilities

• Coordinate day-to-day clinical trial activities from start-up to close-out.
• Schedule and conduct study visits according to protocol requirements.
• Maintain study documentation and ensure informed consent is obtained.
• Monitor patient safety and educate patients on study protocols.
• Accurately enter study data into EDC systems.

Skills

Strong organizational and time management skills

High attention to detail and accuracy in documentation

Excellent interpersonal and communication skills

Ability to manage multiple studies

Proficiency in EDC systems

Proficiency in Microsoft Office Suite

Education

Bachelor’s degree in life sciences, healthcare, or related field

Job description

SerenaGroup, Inc is seeking a Clinical Research Coordinator in Monroeville to oversee crucial aspects of clinical trials focused on advanced wound care and hyperbaric medicine. You will coordinate trials ensuring compliance, support high-quality patient care, and engage with various stakeholders to meet study goals.

The ideal candidate has a Bachelor’s degree and 1-3 years of relevant experience, with strong organizational skills and proficiency in data management systems. Certifications in clinical research are a plus.