Associate Director, Clinical Data Management

About the role

The Associate Director, Clinical Data Management will play a key role in the day-to-day management of Clinical Data Management (CDM) activities. They will represent RevMed CDM in Clinical Team meetings and collaborate closely with other functional leaders to ensure clinical trial success.

Responsibilities

• Timely and professional management of clinical trial data for all relevant phases
• Collaborates with other functional leaders to ensure clinical trial success
• Defines project-level data management strategy
• Identifies requirements for capturing and processing of clinical data ensuring accuracy, consistency, and completeness
• Manages and/or performs data management tasks according to strict quality standards including SAE reconciliation, third party vendor data reconciliation, medical coding processing, protocol deviation collection, query management to identify errors and inconsistencies in clinical data and ensure their resolution
• Provides CDM oversight of outsourced and partner-resourced clinical trials including scoping trials, project management, relationship management, approval of deliverables, and coordination of internal reviewers
• Plans, coordinates, and manages CDM tasks for clinical studies
• Participates and reviews CRO proposals
• Acts as primary liaison with CROs, third party data vendors, EDC vendors
• Reviews clinical protocols and cross functional plans
• Serves as primary reviewer or author of case report forms (CRFs) and CRF completion guidelines
• Oversees and participates in all aspects of EDC database development, testing, maintenance, and lock/unlock
• Ensures Data Management Plans are followed through the course of the studies
• Sets and manages Data Management project timelines
• Provides comprehensive status updates to project team members
• Addresses data issues identified by cross-functional team members, accountable for external data vendor documentation, management, and reconciliation
• Aids in defining and creating data listings, summary table validation, data specifications, and process data transfers in preparation for statistical review and data management audit
• Implements data standardization and maintains data model across projects
• Directly manages and mentors responsibilities for internal data management team members
• Leads department initiatives e.g., development of SOPs

Requirements

• MS, BS/BA degree, or other suitable qualification with relevance to the field
• 11 or more years’ direct experience of designing and running early-stage or late-stage clinical trials
• Knowledge of, and experience with, clinical databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures
• Good working knowledge of ICH, FDA, and GCP regulations and guidelines
• A demonstrable record of strong leadership and teamwork
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment
• Excellent written and verbal communication skills
• Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important
• Experience from industry is essential

Preferred Skills

• Oncology experience, especially in solid tumors
• 5 or more years’ direct line management experience

Benefits

Base Pay Salary Range: $186,000 - $233,000 USD

Pay

Base Pay Salary Range: $186,000 - $233,000 USD

Schedule

Full-time

Qualifications

Required:

• MS, BS/BA degree, or other suitable qualification with relevance to the field
• 11 or more years’ direct experience of designing and running early-stage or late-stage clinical trials
• Knowledge of, and experience with, clinical databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures
• Good working knowledge of ICH, FDA, and GCP regulations and guidelines
• A demonstrable record of strong leadership and teamwork
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment
• Excellent written and verbal communication skills
• Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important
• Experience from industry is essential

Preferred:

• Oncology experience, especially in solid tumors
• 5 or more years’ direct line management experience

Skills

• MS, BS/BA degree, or other suitable qualification with relevance to the field
• 11 or more years’ direct experience of designing and running early-stage or late-stage clinical trials
• Knowledge of, and experience with, clinical databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures
• Good working knowledge of ICH, FDA, and GCP regulations and guidelines
• A demonstrable record of strong leadership and teamwork
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment
• Excellent written and verbal communication skills
• Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important
• Experience from industry is essential
• Oncology experience, especially in solid tumors
• 5 or more years’ direct line management experience

Benefits

Base Pay Salary Range: $186,000 - $233,000 USD

Contact Information

To apply, please send your resume and cover letter to careers@revmed.com. For additional information, please contact privacy@revmed.com.