• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. • Collaborating with investigators and site staff to facilitate smooth study conduct. • Performing data review and resolution of queries to maintain high-quality clinical data. • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

• As a freelance contributor, you will work on a project basis, delivering high-quality analytical insights across several areas, including: Company Profiling: Analysing businesses by collecting and processing financials, and synthesising business, market, and M&A track record overviews • Deal Opportunity Mapping: Forming integrated views on platform and add-on deal opportunities for leading PE clients, supported by our proprietary technology • Sector Research: Contributing to research initiatives and niche sector analyses regularly • Platform Insights: Providing feedback and support for ad-hoc projects aimed at enhancing platform data and project efficiency

• Support clinical trial site feasibility and site selection process • Conduct all aspects of clinical monitoring for clinical trials including conduct of site qualification visits, site initiation visits, routine monitoring visits and close-out visits at clinical trial sites • Support the maintenance of the Investigator Site Files and sponsor Trial Master Files • Conduct all aspects of site management as prescribed in the clinical trial specific functional plans • Prepare accurate and timely trip visit reports • Review progress of clinical trials, especially patient recruitment and clinical trial data capture, and initiates appropriate actions to achieve objectives • Organize and make presentations at Investigator Meetings • Participate in the development of Case Report Forms and clinical trial documents • Act as primary contact for clinical trial supplies and other suppliers (vendors) • Participate in regular clinical trial team meetings • Mentor less experienced or new CRA colleagues • Perform CTM tasks as appropriate and as delegated by the CTM • Proactively contributes to continuous improvement of Clinical Operation specific processes, procedure and templates

• Conduct in-depth research, analysis, interpretation, and evaluation of scientific data, focusing on publications, patents, presentations, and clinical trial results, to contribute to articles on drug discovery topics • Prepare comprehensive articles and reports that detail drug discovery efforts or related developments, ensuring clarity and coherence in presentation • Produce high-quality content with a focus on accuracy and detail, requiring minimal edits before publication • Quickly and accurately prepares chemical schemes, tables, figures, and illustrations using chemical drawing software such as ChemDraw, in line with Drug Hunter’s visual identity • Maintain a general understanding of scientific concepts within organic and medicinal chemistry, biochemistry, molecular biology, pharmacology, and a sense of what is state-of-the-art in each field • Possess an awareness of new developments in industries involved in novel drug discovery, such as the pharmaceutical and biotech industries • Maintain a general familiarity with the biopharma industry, including an understanding of the R&D process from target discovery to commercialization and key players in the industrial ecosystem (key companies, CROs, CDMOs, regulatory bodies, regulatory actions, and commercialization case studies) • Writes and speaks in tones of voice appropriate for audiences of different levels, from students to early-career scientists to industry professionals and investors, with empathy for the underlying needs of the audience • Engage and build relationships with the industrial and academic scientific communities • Develops, prototypes, and deploys concepts for a new series of content and content formats based on reader feedback and industry needs • Fosters a positive culture within the industry and editorial team aligned with the mission and values of the company, prioritizing facts, community, clarity, helpfulness, teamwork, and accountability • Perform other related tasks as necessary to support the ongoing needs of the Scientific Content Team and associated functions