Angelo Parra

Background

About Angelo Parra

With a background in Biology and Psychology and 3+ years of hands-on experience in clinical operations at Castle Biosciences, I bring a cross-functional skill set ideal for roles in clinical trial coordination, regulatory affairs, and biotech project management. I’ve supported cross-team initiatives spanning clinical services, problem resolution, and compliance within a regulated biotech environment. Currently serving as the informal lead and primary point of contact for a specialized internal team, I coordinate execution, escalate barriers, and support stakeholder communication. My foundation in clinical workflows, combined with past roles in operational analysis, operations management, marketing strategy, and quality assurance, allows me to bridge communication between stakeholders, support project execution, and maintain high standards of compliance and care. I thrive in hybrid settings where I can contribute to fast-paced, mission-driven teams in biotech, healthcare, or clinical operations and I’m actively pursuing opportunities aligned with that vision. I’m also willing to travel for roles that require in-person collaboration or site visits. Let’s connect if you’re hiring for:• Clinical Trials Coordinator / Project Associate• Regulatory Affairs Associate / Coordinator• Biotech Project Manager• Clinical Operations Specialist• Hybrid roles in clinical or biotech project execution I’m also open to opportunities outside of these core titles if you believe I’d be a strong fit for a role that benefits from my skills and background, I’m happy to explore it!