Associate Director Data Intelligence
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Job Location:
Rio de Janeiro - Brazil
Monthly Salary:
Not Disclosed
Posted on:
07-11-2025
Vacancies:
1 Vacancy
Job Summary
The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.
ROLE AND RESPONSIBILITIES
- Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Disease so as to maximize Ergomeds revenue and reputation by ensuring that relevant data from available data sources are researched aggregated and available to the Directors of Operational Strategy (DOSs) in the timelines required to prepare and deliver high quality well-research proposals to Ergomeds potential clients.
- Assists with RFP RFI proposal review and response as directed by developing strategically targeted feasibility and related data packages including relevant graphics that support the Win Strategy for new business opportunities.
- Analyzes trial protocols study designs and other project details to determine feasibility within the organizations capabilities and knowledge base and leverages those analyses when presenting feasibility data package.
- Evaluates potential risks challenges and constraints associated with proposed projects with a focus on any potential impact on feasibility activities and recruitment rate projections.
- Researches and analyzes the 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 StrategyOncology 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 preaward 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. Attends bid defense preparation and bid defense meetings as requested.
- Develops cases studies and reports as requested.
- Supports SVP Strategic Solutions and Patient Centricity and/or direct supervisor as needed on projects and activities.
Qualifications :
Degree 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 skill
- 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 Information :
Why 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.
Remote Work :
Yes
Employment Type :
Full-time
Key Skills
- Program assessment
- FDA Regulations
- Manufacturing & Controls
- Program Evaluation
- budget forecast
- Research Experience
- Operations Management
- Research & Development
- Strategic Planning
- Contract Management
- Leadership Experience
- negotiation
About Company
Ergomeds fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. ... View more
