Contract Clinical Science Specialist
Contract duration: Spain (Remote)
Immediately
George Higginson is partnered with a fast-growing late-stage biotech company developing innovative therapies in immunology and inflammatory diseases is looking to appoint a Clinical Science Specialist to join their Development team.
With multiple programs progressing through late Phase II and Phase III clinical trials, the business is entering a pivotal stage of growth and is expanding its Clinical Development group to support ongoing general studies and future regulatory milestones.
Reporting to a Senior Medical Director, this individual will play a key role in clinical trial design, study oversight, data interpretation, and cross-functional collaboration across global development programs.
Provide strategic clinical science support across assigned clinical studies and development programs.
Contribute to clinical trial design and protocol development for global Phase II–III studies.
Conduct clinical review and interpretation of study data, identifying trends, outliers, and protocol deviations.
Act as a key liaison between clinical development, clinical operations, CROs, and medical monitoring teams.
Maintain deep scientific expertise in the relevant therapeutic area, monitoring emerging data and competitive landscape.
MSc or PhD in a scientific discipline (life sciences or related field).
Experience working within biotech or pharmaceutical drug development environments.
Strong understanding of GxP and global regulatory requirements within clinical development.
Demonstrated ability to interpret clinical data and communicate insights to cross-functional stakeholders.
Excellent communication and organizational skills with the ability to work independently and collaboratively in global teams.
Join a high-growth biotech at a pivotal stage of development.
Opportunity to play a high-impact role in late-stage clinical development and regulatory milestones .