Bachelor's degree in Life Sciences or related field; advanced degree preferred.
7+ years of clinical data management experience in biotech or pharma.
Experience managing data for oncology clinical trials.
Expert-level proficiency with Medidata Rave EDC.
Strong knowledge of clinical research processes and regulatory guidelines.
Demonstrated experience in CRO and vendor oversight.
Strong analytical, problem-solving, and project management skills.
Responsibilities
Lead and manage clinical data management for oncology trials to meet project timelines and quality standards.
Provide oversight to CRO teams managing clinical data for assigned studies.
Develop and implement comprehensive data management plans and validation protocols.
Oversee database design and validation using Medidata Rave EDC.
Conduct thorough data reviews to identify trends or issues affecting study outcomes.
Collaborate with cross-functional teams to align data strategies with clinical goals.
Manage and oversee performance of external data management vendors.
Benefits
Maintain SOPs and best practices for data management processes.
Opportunity to work with cutting-edge technologies in oncology trials.
Involvement in high-impact clinical studies with direct implications for patient care.
Full Job Description
Responsibilities:
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards.
Provide strategic oversight and direction to CRO clinical data management teams for assigned studies.
Develop and implement data management plans, case report forms (CRFs), edit checks, and data validation plans in alignment with study protocols and regulatory requirements.
Oversee the design, build, and validation of clinical databases using Medidata Rave EDC, ensuring optimal configuration and functionality.
Conduct thorough reviews of clinical data, identifying trends, inconsistencies, and potential issues that may impact data quality or study outcomes.
Collaborate with cross-functional teams including Biostatistics, Clinical Operations, Safety, and Regulatory to ensure alignment of data management strategies with overall clinical development goals.
Provide oversight, and performance management of external data management vendors.
Maintain SOPs, guidelines, and best practices for clinical data management processes.
Represent the Clinical Data Management function in internal and external meetings, providing expert guidance on data-related matters.
Stay current with industry trends, regulatory requirements, and technological advancements in clinical data management, particularly in the oncology field.
Requirements:
Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred.
minimum of 7+ years of clinical data management experience in the biotechnology or pharmaceutical industry.
Experience managing oncology clinical trials data, including a deep understanding of oncology-specific data requirements and challenges.
Expert-level proficiency with Medidata Rave EDC, including system configuration, form design, and edit check programming.
Strong knowledge of clinical research processes, FDA & ICH guidelines, GCP, GCDMP, and CDISC standards.
Demonstrated experience in CRO and vendor oversight.
Excellent project management skills with the ability to manage multiple studies simultaneously.
Strong analytical and problem-solving skills with meticulous attention to detail.
Outstanding communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders.
Proficiency in Microsoft Office Suite and familiarity with statistical software (e.g., SAS, R) is a plus.
CCDM® (Certified Clinical Data Manager) certification.
Experience with risk-based monitoring in oncology studies.
Knowledge of emerging technologies in clinical data collection and management (e.g., ePRO, wearables, AI/ML applications).
