Associate Director Data Intelligence

Ergomed; Teletrabalho; BRL 160.000 - 200.000; Tempo integral

Resumo da oferta

A global clinical research organization is seeking a Sr. Director/Director of Data Intelligence in Rio de Janeiro. The role involves supporting pre-award feasibility strategies focused on Oncology and Rare Disease, requiring strong clinical research expertise and experience managing external partners. The candidate should have a Life Sciences degree and the ability to distill complex data into actionable insights. Remote work is available, promoting a diverse and inclusive environment.

Serviços

Training and career development opportunities

Friendly supportive working environment

Strong emphasis on personal and professional growth

Qualificações

• Degree educated in Life Sciences or equivalent.
• Clinical research experience in Rare Disease and/or Oncology.
• Global feasibility experience.

Responsabilidades

• Support overall operational strategy globally focusing on Oncology and Rare Disease.
• Assist with RFP RFI proposal review and response.
• Analyze trial protocols and study designs to determine feasibility.

Conhecimentos

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

Formação académica

Degree educated in Life Sciences or equivalent

Descrição da oferta de emprego

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.

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

EXPERIENCE

years

VACANCY

1