Clinical Scientist: Oncology Data Review

CellCentric Limited; United Kingdom; Remote; GBP 45,000 - 65,000; Full time

Job summary

CellCentric Limited is seeking a Clinical Scientist with expertise in clinical data review to enhance our clinical development programs. The successful candidate will be responsible for analyzing clinical data, identifying trends, and ensuring quality oversight. You will collaborate with various teams to support data interpretation and contribute to the success of key study deliverables.

The ideal candidate will possess a strong background in life sciences or medicine, with relevant experience in clinical trial settings, and be adept at working within cross-functional teams.

Qualifications

• Strong scientific or medical background with experience reviewing clinical trial data.
• Experience in haematological oncology, preferably in multiple myeloma.
• Strong understanding of clinical trial conduct, GCP, medical terminology, and clinical data standards.

Responsibilities

• Review clinical, safety, and efficacy data to identify trends and discrepancies.
• Support preparation and review of data listings and dashboards.
• Collaborate with cross-functional teams to support high-quality data review.

Skills

Clinical data interpretation

Collaboration

Attention to detail

Communication skills

Analytical mindset

Education

Degree in life sciences, medicine, pharmacy, or related discipline (MD, PhD, PharmD, or MSc preferred)

Tools

Clinical data review tools

EDC systems

Data visualization outputs

Job description

CellCentric Limited is seeking a Clinical Scientist with expertise in clinical data review to enhance our clinical development programs. The successful candidate will be responsible for analyzing clinical data, identifying trends, and ensuring quality oversight. You will collaborate with various teams to support data interpretation and contribute to the success of key study deliverables.

The ideal candidate will possess a strong background in life sciences or medicine, with relevant experience in clinical trial settings, and be adept at working within cross-functional teams.