Associate Director, Clinical Data Management – Oncology

Summit-Therapeutics

Palo Alto (CA)

On-site

USD 174,000 - 204,000

Full time

14 days+

Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

Summit Therapeutics is seeking an Associate Director of Clinical Data Management to lead data management across global oncology trials, ensure high data quality, integrity, and timely delivery. You will collaborate with Clinical Operations, Biostatistics, Regulatory, and IT to drive standardized processes, manage CROs and staff, and optimize study outcomes.

The role requires 10+ years in CDM, strong regulatory knowledge, and a strategic mindset to advance late-phase programs in a fast-paced

Qualifications

Excellent interpersonal, communication, and leadership skills.
CRO and vendor oversight experience preferred.
Strong knowledge of clinical research, FDA & ICH, GCP, and related regulatory requirements.

Responsibilities

Lead the data management components of a clinical trial from early to late phase.
Direct planning, implementation, and direction of CDM activities including CRF/eCRF design and database lock.
Oversee CROs and vendors, ensuring data quality, integrity, and regulatory compliance.
Develop and implement data standards, data management plans, and data transfer agreements.
Collaborate with cross-functional teams (Clinical Operations, Biostatistics, IT) to achieve study objectives.