[Hiring] Senior Clinical Data Manager @Precision Medicine Group

Role Description

We are hiring a Clinical Data Manager II or Senior Clinical Data Manager to join our global team. We can consider candidates based in Poland, Hungary, Romania, Serbia, or Slovakia.

The Clinical Data Manager II/Senior Clinical Data Manager is responsible for managing all aspects of the clinical trial data management process from study start-up to post-database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs), regulatory directives, study-specific plans, and guidelines will be followed. This position will also oversee and/or perform database development and testing.

• Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring back-up, continuity, responsiveness, and timely task performance.
• Oversee project data entry process including development of data entry guidelines, training, data entry quality, and resourcing.
• May perform quality control of data entry.
• Provide input, assess, and manage timelines. Ensure clinical data management deadlines are met with quality.
• May develop CRF specifications from the clinical study protocol and coordinate review/feedback from stakeholders.
• Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.
• May specify requirements for all edit check types (e.g., electronic, manual data review, edit checks). Oversee development of edit check specifications and manual data review specifications.
• Responsible for creating, revising, appropriate versioning, and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
• Train clinical research personnel on the study-specific CRF, EDC, and other project-related items as needed.
• Review and query clinical trial data according to the Data Management Plan.
• Perform line listing data review based on guidance from the sponsor and/or Lead DM.
• Run patient and study level status and metric reporting.
• Perform medical coding of medical terms to ensure medical logic and consistency.
• Coordinate SAE/AE reconciliation.
• Liaise with third-party vendors such as external data and EDC vendors in a project manager capacity in support of timelines and data-related deliverables.
• May assist with SAS programming and quality control of SAS programs used in the Data Management department.
• Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and stakeholders.
• May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP), and Clinical Study Reports (CSRs), if required by the project.
• Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities.
• May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, and potential client engagement meetings.
• May review Request for Proposals (RFP), proposals, and provide project estimates.
• Provide leadership for cross-functional and organization-wide initiatives, where applicable.
• Train and ensure that all data management project team members have been sufficiently trained.
• Communicate with study sponsors, vendors, and project teams regarding data, database, or other relevant project issues.
• May present software demonstrations/trainings, department/company training sessions, and present at project meetings.
• May require some travel.
• Perform other duties as assigned.

Qualifications

• Bachelors and/or a combination of related experience.
• 8+ years’ experience as a Sr. Clinical Data Manager or 5+ years as a Clinical Data Manager II working for a Clinical Research Organisation, Pharmaceutical, or Biotech company.
• Set up and Database migrations experience.
• Oncology experience preferred.
• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
• Excellent organizational and communication skills.
• Professional use of the English language; both written and oral.
• Experience in utilizing various clinical database management systems.
• Broad knowledge of drug, device, and/or biologic development and effective data management practices.
• Strong representational skills, ability to communicate effectively orally and in writing.
• Strong leadership and interpersonal skills.
• Ability to undertake occasional travel.

Company Description