Neuroscience Clinical Scientist: Data Insights & Strategy

Worldwide Clinical Trials; Buenos Aires; On-site; ARS 119,283,000 - 237,056,000; Full time

Job summary

Worldwide Clinical Trials seeks a Clinical Scientist to lead the review and interpretation of clinical data, communicating findings to clients and study teams. You will work with the Medical Monitor and cross‑functional teams to ensure high data quality and CSR integrity, while contributing to study strategy.

Responsibilities include data review, safety monitoring collaboration, and presenting trends to stakeholders.

Qualifications

• Advanced clinical or scientific degree preferred (e.g., PharmD, PhD, MSN, MPH) with 8+ years of industry‑related neuroscience experience.
• Or Bachelor’s degree with 12+ years of relevant industry/research experience in neuroscience, including data review and interpretation.

Responsibilities

• Develop clinical data review plans for assigned studies.
• Collaborate with cross‑functional study team members to ensure protocol‑defined variables are collected and reported accurately.
• Conduct ongoing review and analysis of clinical data utilizing listings, tables, figures, graphs, and EDC as needed.
• Track and analyze potential safety events in collaboration with Pharmacovigilance and Medical Monitoring.
• Contribute to discussions on potential study or strategy modifications based on clinical data review.
• Create data summary slides for Safety Review Committee Meetings and Data Review Meetings with support from Director.
• Present key data trends and findings to the Medical Monitor, Study Team, and Client.
• Query data on EDC data during Clinical review with timely follow up and identify potential protocol deviations.
• Partner with vendors and study team members to ensure accurate endpoint reporting.
• Serve as a point of contact for site staff and monitors for protocol and clinical inquiries.
• Collaborate with Data Management on CRF design and data quality plans.
• Review data‑driven sections of regulatory and clinical reporting documents (CSRs, INDs, NDAs/BLAs, annual reports, IBs).
• Provide scientific writing support, including patient narratives, abstracts, posters, and presentations.
• Mentor and train junior staff.
• Utilize visual analytics tools to interpret and communicate data insights.

Skills

Clinical data analysis

GCP/ICH knowledge

Presentation skills

EDC proficiency

Data visualization

Travel willingness

Education

Advanced clinical or scientific degree

Bachelor's degree with extensive experience

Tools

EDC systems

MS Office

Data visualization platforms

Job description

Worldwide Clinical Trials seeks a Clinical Scientist to lead the review and interpretation of clinical data, communicating findings to clients and study teams. You will work with the Medical Monitor and cross‑functional teams to ensure high data quality and CSR integrity, while contributing to study strategy.

Responsibilities include data review, safety monitoring collaboration, and presenting trends to stakeholders.