The Principal Clinical Scientist at DELFI Diagnostics will drive scientific planning, strategy, and clinical management of studies, ensuring effective execution and compliance with regulatory standards.
In Short
Lead clinical protocol execution and external research collaborations.
Manage study design, execution, analysis, and reporting.
Oversee vendor selection and management.
Ensure compliance with GCP and ICH guidelines.
Collaborate with cross-functional teams for study success.
Identify and resolve clinical study issues proactively.
Contribute to the generation of Standard Operating Procedures (SOPs).
Maintain audit readiness and compliance.
Establish rapport with external partners and vendors.
Support scientific design and publication of studies.
Requirements
Master’s degree or higher in a science or health-related discipline.
8 years of experience with a Master’s degree or 5 years with a PhD.
Experience in clinical trials and research projects.
Strong analytical skills to interpret data.
Excellent communication and organizational skills.
Ability to manage multiple priorities.
Willingness to travel 10-15% of the time.
Knowledge of medical device clinical trial design preferred.