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Position: ContractClinical Science Specialist

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Contract duration: 6+ months

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Location: Spain (Remote)

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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.

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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.

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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.

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Key Responsibilities:

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- 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.

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Requirements:

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- 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 general teams.

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Why Join?

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- 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. xcskxlj

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If this could be of interest, feel free to reach out directly or apply for a confidential discussion.

Postúlate en Kit Empleo: kitempleo.es/empleo/5t2wnm

📌 Contract Clinical Science Specialist (Almería)
🏢 AL Solutions
📍 Almería