Position: ContractClinical Science SpecialistContract duration: 6+ monthsLocation: Spain (Remote)Start date: Immediately
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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 global 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.
Key Responsibilities: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 .Support development of core clinical documentation including protocols, CRFs, informed consent forms, and clinical study reports .Contribute to regulatory documentation and responses to health authority queries .Assist in preparation of investigator meeting materials, presentations, and study communications .Support scientific engagement activities, including interactions with Key Opinion Leaders (KOLs), congress preparation, and publications.Maintain deep scientific expertise in the relevant therapeutic area, monitoring emerging data and competitive landscape.Contribute to continuous improvement of clinical development processes and systems .
Requirements:MSc or PhD in a scientific discipline (life sciences or related field).Experience working within biotech or pharmaceutical drug development environments .Direct experience supporting Phase II and/or Phase III clinical trials .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 .
Why Join?Join a high-growth biotech at a pivotal stage of development .Work on innovative immunology programs addressing significant unmet medical needs .Collaborate with an experienced leadership team and globally recognized scientific experts .Opportunity to play a high-impact role in late-stage clinical development and regulatory milestones. xiphteb
If this could be of interest, feel free to reach out directly or apply for a confidential discussion.