Sr. Director/Director Data Intelligence

OverviewThe Sr. Director/Director, Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis. ResponsibilitiesSupports overall operational strategy globally, with a focus on Oncology and Rare Disease, ensuring that relevant data from available sources is researched, aggregated, and available to the Directors of Operational Strategy (DOSs) in the timelines required to prepare and deliver high quality, well-researched proposals to Ergomed’s potential clients. Assists with RFP, RFI, proposal review and response by developing strategically targeted feasibility and related data packages, including graphics that support the Win Strategy for new business opportunities. Analyzes trial protocols, study designs, and other project details to determine feasibility within the organization's capabilities and knowledge base, and leverages those analyses when presenting feasibility data packages. Evaluates potential risks, challenges, and constraints associated with proposed projects, focusing on potential impact on feasibility activities and recruitment rate projections. Researches and analyzes current market trends, competitive landscape, and therapeutic area dynamics relevant to each proposed project. Develops and maintains feasibility summaries including relevant graphics for specific indications as requested by the direct supervisor or the SVP, SSPC to minimize rework (e.g., landscape summaries for certain oncology indications as determined by the Director of Operational Strategy Oncology, the Senior Director of Operational and Clinical Intelligence and/or the SVP, SPCC). Documents which feasibility activities and search criteria have been used when transferring pre-award feasibility data packages internally in case of absence to minimize rework or at project handover to post-award feasibility team. Supports the development of processes and solutions to maximize pre-award feasibility package development and integration into the larger win strategy. Tracks and provides information on potential data sources, including return on investment, to support executive investment decisions regarding acquisition of or access to future data sources. Develops materials for bid defenses and attends bid defense preparation and bid defense meetings as requested. Develops case studies and reports as requested. Supports SVP, Strategic Solutions and Patient Centricity and/or direct supervisor as needed on projects and activities. QualificationsDegree educated in Life Sciences or equivalent Clinical research experience in Rare Disease and/or Oncology Global feasibility experience Experience managing external partners Previous experience in a CRO environment Report writing and presentation skills Ability to handle multiple tasks to meet deadlines Ability to access, aggregate and distill data to create targeted data packages to support strategic goals. Additional InformationWhy PrimeVigilance We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer: Training and career development opportunities internally Strong emphasis on personal and professional growth Friendly, supportive working environment Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships Come and join us in this exciting journey to make a positive impact in patients’ lives. We look forward to welcoming your application. #J-18808-Ljbffr