Hiring.Camp

Research Associate I for Scientific Data Curation

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·

Yesterday

Location
Bulgaria, Sofia · France, Lyon
Workplace
Onsite
Type
Full-time
Department
Education
Seniority
Entry
Visa
Not sponsored
Source
Workday

Description

Research Associate I for Scientific Data Curation - Home or office based

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Research Associate I in the MRT Database Team at ICON, you will help maintain and develop high-quality scientific content within the ePROVIDE™ platform. You will curate structured data across three key databases: PROQOLID™, which describes Clinical Outcome Assessments (COAs); PROLABELS™, which captures COA-related endpoint strategies and claims reflected in regulatory labels; and PROINSIGHT™, which describes clinical guidelines and agency recommendations relevant to COAs, endpoint selection, drug development, and health technology assessment.

What You Will Do:

In this role, you will support the accuracy, consistency, and scientific value of ePROVIDE™ by sourcing, reviewing, extracting, and curating information from scientific literature, regulatory labels, clinical guidelines, agency publications, client requests, and internal knowledge sources.

  • Curating accurate, structured scientific data into the ePROVIDE™ platform across PROQOLID™, PROLABELS™, and PROINSIGHT™.
  • Identifying, sourcing, and screening relevant information on COAs, COA endpoint strategies, regulatory label claims, clinical guidelines, and agency recommendations.
  • Extracting and summarising information from scientific publications, regulatory labels, Summary of Product Characteristics documents, public assessment reports, clinical guidelines, and agency-published documents.
  • Applying database-specific rules, scope criteria, taxonomy, and quality standards to ensure scientific consistency, traceability, and data integrity across the platform.
  • Collaborating with internal Database Team members and cross-functional colleagues to support the client-facing and internal use of ePROVIDE™ data.
  • Supporting database updates, quality checks, documentation, and continuous improvement activities to keep ePROVIDE™ content reliable, relevant, and up to date.

Your Profile:

You ideally bring a scientific background, strong attention to detail, and an interest in clinical outcome assessment, endpoint strategy, and structured data curation.

  • Bachelor’s or Master’s degree in a relevant scientific discipline, for example psychology, public health, life sciences, health sciences, pharmacy, biomedical sciences, or a related field.
  • Previous experience in clinical research, health outcomes research, scientific literature review, data curation, or a related field; experience in a pharmaceutical, biotechnology, CRO, academic, or health research environment is an advantage. 
  • Ability to read, interpret, and summarise scientific, clinical, and regulatory information with accuracy and appropriate scientific judgement.
  • Strong attention to detail, consistency, and documentation, with the ability to follow defined rules and quality standards.
  • Flexibility to apply rules consistently while adapting scientific judgement when justified exceptions arise.
  • Good organisational skills and ability to manage several curation tasks or database updates in parallel while respecting timelines.
  • Proactive, independent, locus of control
  • Strong communication and collaboration skills, with the ability to work effectively in a team-based, cross-functional environment.
  • Comfort working with digital platforms, structured databases, and data extraction tools; familiarity with COAs, regulatory labels, clinical guidelines, or endpoint strategy is an asset.
  • Ability to work fully in English within an international department and team environment.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

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