• Interact with biotechnology and pharma clients over email and create specific regulatory and supporting documentation as required • Manage, fact-check and enter data across various research related systems • Respond to any regulatory document requests by looking up the info in our local repository and sending emails back • Organize documentation, and get e-Signatures from respective parties if required • Any administrative tasks which might come up

• Conduct bottom-up fundamental research in innovative, publicly traded healthcare and insurance companies worldwide • Responsible for idea generation, news coverage and data monitoring in your sectors, proactively identifying and calling out opportunities for alpha generation • Perform financial modeling and valuation, using all available data sources to better understand and forecast company KPIs • Cultivate relationships with key sector experts and management teams and participate in major conferences and events • Make BIT Capital’s alternative data, artificial intelligence & quantitative capabilities an integral part of your research process, and identify opportunities to improve such capabilities • Collaborate with other investment team members, such as biotech

• Prepare regulatory and analytical documents, including testimony, schedules, work papers, information requests, and briefs. • Review numeric and non-numeric datasets to identify key data points, trends, and issues. • Perform data sorting and cleaning to identify critical information and discovery issues. • Communicate data analysis through detailed and high-level presentations, including data visualization. • Use public data and data from discovery to perform causational, trend, and risk analysis. • Maintain detailed records of documents, notes, and references for deliverables. • Conduct comparative benchmarking analyses using industry data. • Perform administrative tasks related to projects, such as preparing progress reports, compiling report sections, and updating project schedules. • Other responsibilities as assigned.

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.