Advance your career in clinical research with Alcanza as a Clinical Research Coordinator. This role focuses on the management of studies, patient interactions, and ensuring compliance with industry standards.In this dynamic role, you'll play a key part in managing clinical trials across multiple therapeutic areas including neurology and dermatology. You will ensure effective execution of research protocols while prioritizing patient consent and maintaining accurate documentation throughout study phases. Engage with a team-oriented team to enhance trial effectiveness and participant experiences.Key Responsibilities:Obtain informed consent from study participantsFollow up with patients during trial intervalsManage data entry and query responses in EDCMonitor and resolve study-related issues timelyEnsure compliance with HIPAA and GCP guidelinesRequirements:Minimum 5 years in clinical research or relevant experienceProficiency in basic clinical proceduresStrong organizational and communication abilitiesSelf-motivated and capable of minimal supervisionMust be willing to travel extensivelyUtilize your clinical expertise and organizational skills to contribute to impactful research at Alcanza.

📌 Join Alcanza As Clinical Research Coordinator (Burlington)
🏢 ActivMed Practices & Research
📍 Burlington