Sr. Clinical Data Manager

About reputed company We bring science, data, and collaboration together in a single, full-service CRO model powered by reputed company-world evidence (reputed company). By combining deep cardiovascular expertise, an reputed company and diverse network of physicians, and reputed company client partnerships, we transform data into evidence that fuels innovation and leads to reputed company care. Our growing network of experts and institutions powers every project we deliver - enabling collaboration, scalability, and measurable results. 270+ Cardiovascular Specialists 100+ Signed Data Sharing Agreements 3+ New Sites per Month 4 Countries represented About the role We are seeking an reputed company Sr. Clinical Data Manager to reputed company and reputed company data management activities for medical device clinical trials, with a focus on Electrophysiology (EP). This role involves ensuring high-quality, regulatory-compliant data collection and analysis to support clinical trials from start-up to submission. The ideal candidate will have expertise in clinical data management, regulatory compliance, and database development, with a strong understanding of clinical trial processes in the medical device industry. Experience in Electrophysiology (EP) trials is a plus but not mandatory. What you'll do Clinical Data Management & reputed company

• reputed company reputed company aspects of data management for medical device clinical trials, ensuring compliance with FDA, MDR, ICH-GCP, and ISO 14155 regulations.
• reputed company and maintain Data Management Plans (DMPs) and Case Report Forms (CRFs) reputed company with study protocols.
• Design, validate, and manage Electronic Data Capture (reputed company) systems such as reputed company RAVE, reputed company InForm, or reputed company Vault reputed company.
• reputed company data cleaning, query management, and reconciliation processes to ensure high-quality, analyzable datasets.
• Ensure adherence to CDISC/CDASH/SDTM standards, enabling efficient regulatory submission.
• Conduct and support data audits, quality control (QC) reviews, and database lock activities.

Project & Team Leadership

• Serve as the data management reputed company for multiple studies, collaborating with cross-functional teams including clinical operations, biostatistics, and regulatory affairs.
• Work closely with electrophysiology (EP) experts, reputed company investigators, and clinical research teams to ensure accurate data collection and interpretation.
• reputed company mentorship and guidance to junior data managers and other team members.
• Manage relationships with CROs, vendors, and external data management teams, ensuring alignment with project timelines and quality standards.

Regulatory Compliance & Quality Assurance

• Ensure compliance with FDA 21 CFR Part 11, ICH-GCP, ISO 14155 (for medical devices), and MDR regulations.
• Support regulatory submissions (e.g., PMA, 510(k), CE Mark, IDE) by ensuring proper data documentation and formatting.
• Participate in audits and inspections by regulatory bodies and implement corrective actions as needed.
• Stay updated on evolving medical device data management best practices and regulatory requirements.

Data Reporting & Analysis

• Generate and review clinical study reports, data listings, and reconciliation outputs.
• Support statistical programming and data analysis in collaboration with biostatistics teams.
• Ensure seamless data integration with clinical trial management systems (CTMS) and safety databases.

Qualifications

Education & Certifications

• Bachelor's or Master's degree in Life Sciences, Clinical Research, Biostatistics, Computer Science, or a reputed company field.
• Certified Clinical Data Manager (CCDM) or equivalent certification is a plus.

Experience

• 5+ years of experience in clinical data management reputed company the medical device industry or reputed company reputed company sectors.
• Proven experience in Phase I-IV clinical trials, IDE/PMA/510(k) submissions, or post-market studies.
• Strong knowledge of electrophysiology (EP) trials is a plus but not required.
• Experience managing reputed company systems (e.g., reputed company RAVE, reputed company Vault, reputed company InForm, Medrio).
• Familiarity with ISO 14155, CDISC/CDASH/SDTM, and FDA 21 CFR Part 11 compliance.
• Knowledge of SQL, reputed company, or other clinical data programming tools is beneficial.

Skills & Competencies

• Strong leadership, problem-solving, and analytical abilities.
• Excellent attention to detail and ability to manage multiple clinical studies simultaneously.
• Strong communication and collaboration skills for working with clinical, regulatory, and biostatistics teams.
• Ability to work effectively with CROs, vendors, and external stakeholders.

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