Lead Clinical Data Manager

Katalyst CRO; Durham (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading contract research organization is seeking a Clinical Data Manager to oversee oncology trials. The role includes leading data management activities, developing data management plans, and collaborating with various teams to ensure project success. Candidates should have at least 7 years of experience in clinical data management, a Bachelor's degree in Life Sciences or a related field, and expertise in Medidata Rave EDC. Strong analytical and communication skills are also essential. This position is based in Durham, NC.

Qualifications

• 7+ years of clinical data management experience in biotechnology or pharmaceutical industry.
• Experience in managing oncology clinical trials including oncology-specific data challenges.
• Expertise in Medidata Rave EDC with form design and configuration skills.

Responsibilities

• Lead data management activities ensuring project timelines and quality standards.
• Develop and implement data management plans and case report forms.
• Collaborate with cross-functional teams to align data management strategies.

Skills

Clinical data management

Project management

Analytical skills

Communication

Problem-solving

Team collaboration

Education

Bachelor's degree in Life Sciences or related field

Advanced degree preferred

Tools

Medidata Rave EDC

Microsoft Office Suite

Statistical software (e.g., SAS, R)

Job description

Overview

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.

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.
• A 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)