CDM Strategy Lead for Global Oncology Trials

Summit Therapeutics Inc.; Palo Alto (CA); Hybrid; USD 174,000 - 205,000; Full time

Benefits offered by this job

Competitive compensation

Job summary

Summit Therapeutics Inc. is seeking an Associate Director, Clinical Data Management to lead data management for diverse clinical trials. You will design eCRFs, oversee databases, and ensure high-quality data for analyses, collaborating with biostatistics, clinical, and regulatory teams across global studies.

The role requires a strong background in CDM, regulatory requirements (FDA/ICH), and extensive leadership of data management staff and CRO partners.

Qualifications

• Bachelor’s degree in Life Sciences, Computer Science, or relevant field of study.
• Minimum of 10+ years of Clinical Data Management experience, oncology preferred.
• Experience with various EDC systems and regulatory coding processes.
• Strong line management and leadership skills; CRO oversight experience is a plus.

Responsibilities

• Lead data management components across small to large global trials.
• Oversee CDM staff, CROs, and vendors; ensure data quality and timely delivery.
• Design and manage eCRF, data standards, and data transfer agreements.
• Collaborate with Clinical Operations, Biostatistics, Regulatory, and IT to ensure regulatory compliance.

Skills

Data management

CDM leadership

Regulatory knowledge

EDC systems

Team leadership

Education

Bachelor’s degree in Life Sciences or related field

Tools

EDC systems

MedDRA/WHODRUG coding

Job description

Summit Therapeutics Inc. is seeking an Associate Director, Clinical Data Management to lead data management for diverse clinical trials. You will design eCRFs, oversee databases, and ensure high-quality data for analyses, collaborating with biostatistics, clinical, and regulatory teams across global studies.

The role requires a strong background in CDM, regulatory requirements (FDA/ICH), and extensive leadership of data management staff and CRO partners.