Principal Clinical Scientist, Clinical Science Analytics & Insights

buscojobs España; Sevilla; A distancia; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company is seeking a Principal Clinical Scientist to manage clinical science functions remotely across several countries, including Spain. The role involves overseeing data insights and ensuring compliance with clinical standards, requiring extensive experience in clinical research and leadership.

Formación

• At least 8 years of clinical research experience.
• Minimum 1 year of leadership experience.

Responsabilidades

• Lead CSAI services implementation per study scope.
• Manage data cleaning processes to support study deliverables.
• Oversee Medical Monitor review of subject data.

Conocimientos

Leadership

Communication

Analytical Skills

Negotiation

Educación

Bachelor’s degree in a science or health-related field

Herramientas

EDC systems

Data visualization tools

Descripción del empleo

Principal Clinical Scientist, Clinical Science Analytics & Insights

Location: Remote, Spain

Precision for Medicine is seeking an experienced Principal Clinical Scientist to work remotely across Poland, Hungary, Serbia, Romania, Slovakia, Spain, or the UK.

Position Summary :

The Principal Clinical Scientist should possess a strong knowledge of medical and oncology standards relevant to clinical trials, especially in solid and liquid tumor areas. The role involves managing the operational clinical science functions from study start-up to database lock, focusing on scientific and indication-specific data insights, visualization, and data cleaning as part of the cross-functional review team. The candidate must have a medical-related degree (e.g., RN, OCN, RPH, PharmD).

Essential functions include but are not limited to :

1. Leading CSAI services implementation per study scope.
2. Providing scientific expertise in data capture, review, and cleaning.
3. Supporting process development for integrated data cleaning across departments.
4. Managing data cleaning processes to support study deliverables.
5. Overseeing Medical Monitor review of subject data.
6. Reviewing protocols from an operational scientific perspective.
7. Contributing to the development of study documentation such as eCRF specifications and edit checks.
8. Supporting data management activities, including UAT testing.
9. Facilitating cross-departmental communication regarding data review and updates.
10. Identifying and managing study risks and deficiencies.
11. Supporting project and budget management activities.
12. Ensuring proper documentation in eTMF.
13. Conducting scientific data reviews using programmed outputs and guidelines.
14. Managing queries and providing status updates on data review findings.
15. Developing and conducting UAT for CSAI outputs.
16. Providing training for CSAI team members and study sites.
17. Participating in study meetings and presentations.
18. Supporting study-specific committees and review processes.
19. Participating in candidate interviews and business development activities as needed.
20. Performing other duties as assigned.

Qualifications :

• Bachelor’s degree or equivalent in a science or health-related field with proficiency in medical terminology.
• At least 8 years of clinical research experience or equivalent competencies.
• Minimum 1 year of leadership experience.

Other Requirements :

• Experience in oncology, with knowledge of clinical standards and side effects.
• Experience across trial phases I-III.
• On-site monitoring or data review experience preferred.
• Proficiency with EDC systems and data visualization tools.
• Excellent command of English, both written and spoken.
• Knowledge of FDA and ICH/GCP regulations.
• Ability to travel domestically and internationally as needed.

Highly Preferred :

• Medical degree (RN, OCN, RPH, PharmD, etc.).
• Experience in database building.

Competencies and Skills :

• Advanced oncology and medical terminology knowledge.
• Continuous learner with self-research skills.
• Understanding of clinical trial regulations and processes.
• High ethical standards and integrity.
• Ability to independently manage operational functions globally.
• Strong communication, negotiation, and analytical skills.
• Self-motivated with remote work capability.
• Flexible, results-oriented, and accountable.
• Financial management skills at project level.
• Excellent presentation and communication skills.

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