Principal Clinical Scientist, Clinical Science Analytics & Insights

Tbwa Chiat / Day Inc; Pamplona; A distancia; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in clinical research is seeking a Principal Clinical Scientist to manage clinical science functions for oncology trials. The role requires expertise in medical standards and strong leadership skills. The candidate will oversee data insights and ensure compliance with clinical guidelines while collaborating across departments. Ideal for experienced professionals with a background in clinical research and oncology.

Formación

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

Responsabilidades

• Leading CSAI services implementation on assigned projects.
• Managing data cleaning process to support study deliverables.
• Providing scientific input during protocol reviews.

Conocimientos

Oncology

Medical Terminology

Communication

Time Management

Negotiation

Conflict Resolution

Educación

Bachelor’s degree in science or health-related discipline

Medical degree such as RN, OCN, RPH, PharmD

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 in 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 tumors. They will manage the operational clinical science functions from study start-up to database lock for assigned projects, focusing on scientific and indication-specific data insights, visualization, and data cleaning as part of the cross-functional review team. The role requires serving as a subject matter expert in clinical knowledge, guidelines, and standards of care for clinical trial data review. A medical-related degree (RN, OCN, RPH, PharmD, etc.) is required.

Key Responsibilities include but are not limited to:

1. Leading CSAI services implementation per study scope on assigned projects.
2. Providing scientific input on data capture, review, and cleaning processes.
3. Supporting the development of process flows for integrated data cleaning across departments.
4. Managing the data cleaning process to support study data deliverables.
5. Reviewing subject data with Medical Monitors.
6. Providing scientific input during protocol reviews and in the development of study documentation.
7. Supporting EDC UAT and collaborating on cross-departmental communication.
8. Identifying and managing study risks and CSAI study-specific deficiencies.
9. Supporting project and budget management activities.
10. Ensuring proper documentation and supporting data review activities, including training and meetings.
11. Participating in review of TLFs and CSRs, and potentially in business development activities.

Qualifications:

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

Additional Requirements:

• Oncology therapeutic experience, with knowledge of clinical standards of care, biomarkers, and side effects.
• Experience across trial phases I-III.
• On-site monitoring or data review experience preferred.
• Experience with EDC systems and data visualization tools.
• Proficiency in computer skills and professional English communication.
• Knowledge of FDA & ICH/GCP regulations.
• Ability to travel domestically and internationally.

Preferred Qualifications:

• Medical degree such as RN, OCN, RPH, PharmD.
• Experience with database build.

Skills and Competencies:

• Advanced oncology and medical terminology knowledge.
• Continuous learner with research and self-education skills.
• Understanding of clinical trial processes and regulatory requirements.
• High integrity, independence, and strategic thinking.
• Excellent communication, time management, negotiation, and conflict resolution skills.
• Motivated, flexible, and results-oriented with financial acumen.

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