Jessica Claire
  • , , 100 Montgomery St. 10th Floor
  • H: (555) 432-1000
  • C:
  • Date of Birth:
  • India:
  • :
  • single:
Successful and experienced competitive intelligence professional with extensive drug development knowledge in numerous therapeutic areas. Fifteen years experience in pharmaceutical CI with a background in research both academic and industry. Organized and efficient, accustomed to working in a fast-paced environment on multiple projects within tight deadlines to produce high quality reports on time, within budget.
  • Pharmaceutical competitive intelligence
  • Primary/secondary research
  • Drug development/brand & commercialization strategy
  • Global medical conference coverage
  • Evaluation of key issues & market trends/development
  • Expert proficiency Word, Excel, Power Point
  • Academic, Reporting
  • Ad, Research
  • Analyst, Scientific
  • API, Strategy
  • Budgets, Strategy development
  • Budget, Strategic
  • Business development, View
  • Competitive, Website
  • Competitive intelligence, Workshops
  • Contracts
  • Clients
  • Client
  • Delivery
  • Editing
  • Edit
  • Focus
  • Forms
  • Functional
  • Leadership
  • Market
  • Materials
  • Messaging
  • Excel
  • Power Point
  • Word
  • Positioning
  • Presenting
  • Presentations
  • Project management
  • Proposals
  • Proposal
  • Quality
  • Quick
  • Relationship management
Senior Consultant, IP & Life Sciences, 12/2014 - Current
Clarivate Analytics City, STATE,
  • Contribute to overall global pharmaceutical life sciences solutions portfolio with focus on competitive intelligence in all therapeutic indications.
  • Lead and support client relationship management, lead generation and business development, proposal and solution methodology development, project delivery, project management, thought leadership, licensing, API and generic strategy and monitoring and group strategy development and implementation.
  • Work with global internal and external cross functional teams to deliver actionable intelligence with the most comprehensive and accurate view of the competition in the highest quality reports to clients.
  • Key Achievements.
  • Major projects include competitive landscape and strategy projects, requiring coordination of a global team, external vendors, extensive primary and secondary research, generic competition and monitoring
  • Created in depth competitive landscapes and commercial assessments in all therapeutic indications
  • Developed and created target product profiles
  • Evaluated and assessed key catalysts and deals for market entry and drug development strategy
  • Managed and supported global teams to develop strategy and solutions for clients
  • Brought in house FTE contract from major pharmaceutical company; embedded as team member for oncology
  • Mentored junior team members to ensure top quality client deliverables
  • Prepared proposals, bids and capabilities presentations.
  • Introduced new department offerings and capabilities
  • Developed and maintained relationships with industry experts
  • Created interview guides and conducted primary research with KOLs, payers and industry experts
  • Managed multiple projects on tight timelines while delivering high quality reports.
  • Main point of contact for client from project inception to delivery and follow up
  • Developed extensive knowledge of key issues and trends as they relate to current and future development in the pharmaceutical and healthcare industries
Associate Director of Oncology Projects, 06/2006 - 08/2013
Pennside Partners City, STATE,
  • Provide scientific input and commercial insights and competitive intelligence to clients at major pharmaceutical companies.
  • Develop brand specific strategy, product positioning and messaging consistent with client needs.
  • Use primary and secondary research to create and present top quality CI reports for all levels of medical/pharmaceutical professionals.
  • Manage multiple projects within tight and evolving timelines.
  • Manage and coordinate team members to complete medical conference coverage and reporting.
  • Developed KITs and KIQs for projects according to client objectives.
  • Key Achievements.
  • Promoted to higher level positions three times over a seven year period.
  • Established and maintained relationships with global key opinion leaders, investigators, academic researchers.
  • Broad knowledge in numerous therapeutic indications with a strong science background providing a high level of expertise to clients.
  • Managed client interactions to ensure successful completion of projects within budget and timelines.
  • Coordinated project team to ensure that goals and deliverables are met and align with client requirements.
  • Performed top line executive analysis of primary and secondary data of marketed drugs and drugs in development highlighting their potential to affect the medical treatment paradigm and commercial success.
  • Managed global primary and secondary market and scientific research.
  • Integrated primary and secondary research to provide strategic recommendations to product and brand teams.
  • Developed and maintained extensive competitive landscapes in oncology, endocrinology, neurology, etc.
  • Created educational materials for workshops and war games.
  • Provided therapeutic background material for client proposals and work orders.
  • Led and conducted client presentations.
  • Created an expansive bibliography of sources from extensive secondary research including literature searches, analyst reports, medical conference proceedings.
  • Managed and coordinated external contractors for team expansion as needed.
  • Held leadership role in the redesign of the company website and blog resulting in significantly increased traffic and acquisition of new clients.
  • Routinely performed ad hoc client requests with 24 hour turn around time.
  • Identified in-licensing opportunities.
  • Excellent track record of creating and presenting high quality reports resulting in renewed contracts and acquisition of new clients.
Clinical Documents Specialist, 02/2004 - 06/2006
BMA Associates City, STATE,
  • Full responsibility of reviewing, editing and writing regulatory documents for of all phases clinical trials.
  • Therapeutic areas include oncology, infectious disease, endocrinology, cardiology Key Achievements.
  • Developed system to efficiently review clinical trial consent forms enabling the group to review, edit and negotiate language revisions with sites for a quick turnaround.
  • Incorporate requested revisions to consent forms and contracts.
  • Negotiated contracts between sponsor and sites, editing language as necessary.
  • Negotiated budgets with clinical trial sites within tight guidelines on behalf of sponsor.
  • Acted as a liaison between the sponsor and the site staff for clinical trial documents.
Education and Training
: , Expected in
Pennsylvania College of Podiatric Medicine - Philadelphia, Pennsylvania
Masters: , Expected in
Tarleton state University - Stephenville, Texas
BA: Biology, Expected in
Russell Sage College - Troy, New York

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Resume Overview

School Attended

  • Pennsylvania College of Podiatric Medicine
  • Tarleton state University
  • Russell Sage College

Job Titles Held:

  • Senior Consultant, IP & Life Sciences
  • Associate Director of Oncology Projects
  • Clinical Documents Specialist


  • Masters
  • BA

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