Clinical Scientist Director - Late Development, Inflammation at Jobgether – Spain
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About This Position
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Scientist Director - Late Development, Inflammation in Spain.
This is a high-impact leadership role at the forefront of clinical development, focused on advancing innovative therapies in the field of inflammation. You will play a pivotal role in late-phase clinical programs, ensuring the translation of scientific strategies into high-quality clinical execution. Working within a dynamic, cross-functional environment, you will oversee trial integrity, data quality, and regulatory alignment. The position offers the opportunity to collaborate with global experts while contributing to life-changing treatments. With strong exposure to decision-making processes and strategic development, you will help shape the future of patient care. This role combines scientific expertise, operational excellence, and leadership in a fast-evolving healthcare landscape.
- Act as a scientific and clinical expert within the assigned therapeutic area, ensuring excellence in protocol execution and data integrity across late-stage clinical trials
- Translate clinical strategies into actionable study designs, including development of protocols, study documents, and operational plans
- Provide oversight and guidance on clinical trial execution, including collaboration with CROs, consultants, and cross-functional teams
- Lead clinical data review, analysis, and interpretation to ensure accuracy, completeness, and regulatory compliance
- Support medical monitoring activities, identifying trends, risks, and emerging issues at the patient and study level
- Ensure high standards of data quality through continuous monitoring, validation processes, and adherence to Good Clinical Practice
- Contribute to regulatory submissions, scientific publications, and presentations, effectively communicating complex clinical data
Requirements:
- Advanced degree in life sciences or healthcare (PhD, MD, PharmD, or equivalent), or relevant combination of education and experience
- Significant experience in clinical drug development, with a strong focus on late-phase trials, preferably within inflammation or related therapeutic areas
- Proven expertise in clinical trial design, execution, and data analysis in compliance with regulatory standards
- Strong understanding of clinical data management processes, including data cleaning, database lock, and reporting outputs
- Experience contributing to regulatory submissions and scientific publications
- Proficiency with clinical data analysis tools (e.g., Spotfire or similar) is highly desirable
- Excellent communication and presentation skills, with the ability to convey complex scientific information to diverse stakeholders
- Demonstrated ability to collaborate effectively in cross-functional, global teams
Benefits:
- Comprehensive and competitive total rewards package including healthcare, financial, and wellness benefits
- Flexible working arrangements to support work-life balance
- Opportunities for continuous learning, career progression, and internal mobility within a global organization
- Inclusive and diverse workplace culture that encourages innovation and collaboration
- Exposure to cutting-edge research and development in a purpose-driven environment
- Access to global teams and resources, fostering professional growth and impact