Associate Director, Clinical Scientist

Responsibilities

• Active Data Surveillance: Conduct daily reviews of the clinical trial data to monitor specific data entries, including patient diary scores, and relevant laboratory markers.
• Data Integrity & Resolution: Identify missing data points or clinical anomalies and proactively coordinate with internal teams and clinical sites to ensure timely resolution and data accuracy.
• Visualization & Reporting: Export and compile data in high-quality visual representations (e.g., Excel, GraphPad, or similar) to track patient progress and treatment patterns.
• Clinical Narrative Development: Synthesize information from various sources, including clinical data, background therapies, and patient history to develop comprehensive longitudinal narratives for individual study participants.
• Strategic Collaboration: Present data findings and analytical "thought constructs" to the clinical leadership team to stimulate discussion and inform development strategy.
• Site Engagement: Facilitate targeted communication with investigators and study sites to clarify clinical observations and ensure the appropriate management of patient transitions on or off therapy.

Qualifications And Experience

• Advanced degree (PhD, PharmD, or MD) in a scientific or life sciences discipline.
• Minimum of 5 years of clinical development experience within the biopharmaceutical industry; a strong understanding of clinical trial methodology and the analysis of clinical data is required.
• Demonstrated expertise in data visualization and analysis.
• Must be highly proficient in Excel and capable of creating professional-grade figures and presentations for internal stakeholders.
• Strong ability to identify trends, ask probing questions, and look beyond the surface of the data to understand the underlying clinical story.