Senior Analyst
4 weeks ago
Confident decisions driven by deep expertise and tenacious research.
Everest Group is a research firm helping business leaders confidently navigate today's market challenges, driving maximized operational and financial performance and transformative experiences. Our deep expertise and tenacious research focused on software, technology, business processes, and engineering through the lenses of talent, sustainability, and sourcing delivers precise and action-oriented guidance. For more information, visit www.everestgrp.com.
Job Overview
The Clinical Development Technologies (ClinTech) team focuses on current and anticipated trends in life sciences (pharmaceuticals, biotechnology, and medical devices) clinical development and the impact of those trends on the software products and platforms. The ClinTech team advice life sciences enterprises and product/platform providers on how the clinical development technology stack should evolve. From our published reports to custom decision support, ClinTech team supports clients though its fact-based data and insights to analyse and assess market trends and topical issues (such as decentralized clinical trials, EHR to EDC, increased use of analytics, etc.) and product provider capabilities.
This is an exciting industry segment, and the Senior Analyst will be expected to analyse developments in the clinical development space due to changing regulations, cutting edge technologies, and new type of therapies (e.g., cell and gene therapies). The Senior Analyst is expected to contribute to the research program by delivering high quality, original research reports and custom advisory projects. This will require the candidate to maintain an ongoing dialog with senior industry executives on key issues, as well as help answer their queries. The candidate will be required to deliver custom research engagements within the clinical development area and occasionally in other areas in life sciences.
Key responsibilities
- Identify areas of research based on industry and client needs
- Problem solving and structure work to manage deliverables and timelines
- Contribute significantly to the published research agenda of the ClinTech practice
- Lead medium sized custom research engagements
- Actively develop domain expertise across ClinTech, leveraging subject matter experts, and external sources
- Support business development efforts through proposal writing and other initiatives
- Participate proactively in external market communication by responding to analyst inquiries, conducting executive conversations, and maintaining/growing long-term client relationships
Skills & Activities
- Strong problem-solving skills and analytical capability, and high levels of intellectual curiosity
- Strong oral and written communication skills with attention to detail
- Project management skills: self-motivated, ability to multi-task, work under pressure and successfully manage deadlines
- Ability to interact and effectively work with others in a team environment. Long term desire to contribute to business growth and build a career as a business leader
- Ability to pick up new areas in ClinTech and build expertise
- Desire to be in a non-hierarchical, entrepreneurial environment; comfort with ambiguity
- Proficient in Microsoft office (PowerPoint, Word, Excel, and Outlook)
Education & Experience
- Bachelor's degree, MBA preferred (preferably from Tier-1 B-School)
- Strong understanding of the clinical development value chain (how do clinical trials work, what are the processes involved, how do CROs come into the picture, etc.) Experience or understanding of clinical development products (e.g., EDC, CTMS, eCOA, etc.) is not mandatory but is a plus
- 1 to 4 years work experience as one of the following:
- Consultant advising pharma companies on product/platform selection in clinical development
- Individual contributor with primary experience working on pharma R&D projects and advising pharma companies on clinical trial processes (e.g., process optimization / mapping, R&D digital transformation, site selection strategy, accelerating clinical development, etc.)
- Experience with pre-sales solutioning and RFP responses to pharma R&D RFPs
- Experience with primary and secondary research focused on drug pipelines, pharma R&D intelligence, clinical trial therapeutic area trends, etc.
- History of excellence in academics, personal and vocational achievements
Everest Group complies with the GDPR, CCPA/CPRA and other data protection regulations. For more information on how Everest Group processes your personal information, please read our Privacy Notice (www.everestgrp.com/privacy-notice-for-applicants-employees-and-contractors/). By submitting this application, you indicate that you have read and understand our privacy terms and consent to the processing of your personal information by us. To exercise your data subject rights under GDPR, CCPA/CPRA you can fill in our form available at Data Rights – Everest Group (everestgrp.com). You can email your data protection request to privacy@everestgrp.com. Everest Group is an equal opportunity employer. We have a culture of inclusion, and we provide equal opportunities for all applicants and employees, including those with disabilities. We are committed to providing an environment that is free of all discrimination and harassment and to treating all individuals with respect.
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