Principal Clinical Scientist, Clinical Science Analytics & Insights

Tbwa Chiat / Day Inc; Málaga; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A healthcare research organization is seeking an experienced Principal Clinical Scientist to manage clinical science functions remotely from Spain. In this role, you will oversee data collection and scientific insights for oncology clinical trials, requiring a solid background in medical standards and at least 8 years of a clinical research experience. A Bachelor’s degree in a relevant field is essential. This position demands strong leadership and communication skills, with opportunities for professional growth.

Formación

• Minimum 8 years of clinical research experience or equivalent competencies.
• At least 1 year of leadership experience is required.
• Good command of English, both written and spoken.

Responsabilidades

• Lead CSAI services for assigned projects.
• Support project teams with scientific data review.
• Manage data cleaning processes for study deliverables.
• Conduct scientific data reviews using programmed outputs.

Conocimientos

Project management

Clinical data review

Oncology standards knowledge

Communication skills

Time management

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 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. The role involves managing the operational clinical science functions from study start-up to database lock, focusing on data collection, visualization, and supporting scientific insights. The candidate will serve as a subject matter expert in clinical data review, applying clinical guidelines and standards of care. A medical-related degree (RN, OCN, RPH, PharmD, etc.) is required.

Key Responsibilities:

• Lead CSAI services per study scope for assigned projects.
• Support project teams with scientific data review and cleaning.
• Develop and implement processes for integrated data cleaning across departments.
• Manage data cleaning processes to support study deliverables.
• Oversee Medical Monitor review of subject data.
• Review protocols from a scientific operational perspective.
• Contribute scientific input to data management, including eCRF specifications and UAT.
• Coordinate communication across departments regarding data review and updates.
• Identify and manage study risks and deficiencies.
• Assist in project and budget management activities.
• Ensure documentation compliance in eTMF.
• Conduct scientific data reviews using programmed outputs and review queries.
• Provide training and participate in study meetings and presentations.
• Support study-specific committees and review reports as needed.
• Participate in candidate interviews and business development activities.

Qualifications:

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

Additional Requirements:

• Experience in oncology and clinical data review.
• Involvement in Phase I-III trials.
• On-site monitoring or data review experience preferred.
• Proficiency with EDC systems and data visualization tools.
• Good command of English language, both written and spoken.
• Knowledge of FDA and ICH/GCP regulations.
• Willingness to travel domestically and internationally.

Preferred Qualifications:

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

Skills and Competencies:

• Advanced oncology and medical terminology knowledge.
• Commitment to ongoing learning in oncology standards.
• Understanding of clinical trial regulations and processes.
• High ethical standards and integrity.
• Ability to manage operations independently in a global environment.
• Strong time management, negotiation, and communication skills.
• Self-motivated, flexible, and results-oriented.
• Financial management skills at project level.

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