Job Title: Clinical Research Associate
Company: ProPharma Group
About ProPharma:
For the past 20 years, ProPharma has been at the forefront of improving patient health and wellness by providing expert advice and services. As the world’s largest Research Consulting Organization (RCO), we empower biotech, medical device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies. Through our advise-build-operate model, we support clients across the entire product lifecycle with deep expertise in regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology. Our customizable consulting solutions are designed to de-risk and accelerate high-profile drug and device programs.
Job Summary:
The Clinical Research Associate (CRA) will be responsible for overseeing clinical monitoring for assigned protocols and investigational sites. This role ensures that studies are conducted and documented in accordance with study protocols, standard operating procedures (SOPs), Good Clinical Practices (GCP), and other applicable regulatory requirements.
Essential Functions:
Necessary Skills and Abilities:
Educational Requirements:
Experience Requirements:
Diversity and Inclusion:
ProPharma celebrates diversity and is committed to creating an inclusive workplace where every individual can be their authentic self. We encourage employees to unleash their innovative, collaborative, and entrepreneurial spirits. As an Equal Opportunity Employer, we provide a safe space where all employees are empowered to succeed.
Application Instructions:
ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please refrain from calling or emailing regarding this posting.
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