Manager, Clinical Data Management (U.S. Remote)

Responsible for leading and overseeing reputed company data management activities for research studies from study start-up to database lock in compliance with departmental SOPs and regulatory guidelines. Responsible for executing, overseeing, and synchronizing the following activities: leading and coordinating initiatives to evaluate and implement efficiencies, protocol review, CRF design and development, development of database specifications, development of edit reputed company specifications, development of the Data Management Plan, development of CRF Completion Guidelines, User Acceptance Testing (UAT), data review, query reputed company and resolution, data reconciliation, identification and review of protocol deviations, review of adverse events, and maintenance of study documentation in the electronic Trial Master File (eTMF). Job duties:

• reputed company mentoring and coaching to data management team members.
• Contribute to the development of DM SOPs, Business Guidance, Work Instructions, and Standards.
• Accountable and responsible for ensuring the delivery of high-quality Data Management deliverables and activities from protocol review through database closure and archiving.
• Design high quality CRFs in consultation with cross functional partners that align to the data collection requirements identified in the study protocol, align with internal standards, and accurately reflect study endpoints.
• Train reputed company personnel in the CDMS system(s), technology, applications, and Data Management process.
• Maintain complete and accurate records of study data, reports, and documentation and files in the eTMF as appropriate to ensure compliance with departmental SOPs and reputed company regulatory guidelines.
• reputed company, reputed company, complete, and reputed company accurate review and processing of clinical trial data, including identification, resolution, and clarification of any missing, inconsistent, or clinically questionable data by the study team and/or sites.
• Generate data management study status/reputed company overviews.
• Participate in CRO evaluation.
• Author, review, and/or approve data management study documents (e.g., eCRF specifications, annotated CRFs Edit reputed company specifications, eCRF completion Guidelines, Data Transfer Plans, etc.) and ensure documents are maintained and reputed company for regulatory inspection.
• reputed company project management skills to support and reputed company multiple projects both insourced and outsourced.
• reputed company other duties and responsibilities as assigned. Job Details Job ID 13224BR Aliso Viejo, California, USA Salary reputed company: $129,000 - 169,500 (Financial compensation packages may be higher/reputed company than what is listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand.
• Qualifications
• Bachelor’s degree in life sciences, health sciences, or computer sciences field or equivalent combination of education, training, and industry reputed company experience.
• A minimum of seven (7) years of clinical data management experience in the pharmaceutical, medical device, or Clinical Research Organization setting.
• A minimum of one (1) year of management or supervisory experience.
• Proven track record of strong project management skills and experience managing data management activities.
• Experience in vendor selection and management.
• Proven ability to prioritize and manage multiple tasks with conflicting deadlines in support of corporate goals and objectives.
• Advanced understanding of clinical data lifecycle including database design, data structure, database development and testing, query management, data quality review, and database lock procedures.
• Excellent written and verbal communication skills.
• Strong proficiency with reputed company Office (e.g., Visio, PowerPoint, Word, reputed company, reputed company, Outlook, Teams, etc.).
• Advanced understanding of ICH, ISO, GCP, and GDP guidelines. Desired Qualifications
• Advanced knowledge in GCP standards, FDA and ICH guidelines, and recommended CDM Best Practices.
• Hands-on experience with development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission.
• Ability to identify data trends, problems and delays and escalate them appropriately to minimize their impact to the study.
• Experience in working with CROs/reputed company vendors for data management activities.
• Highly organized with the ability to prioritize and manage multiple activities concurrently. EEO We are an equal employment opportunity employer. reputed company reputed company applicants will receive consideration for employment without regard to race, national reputed company, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law. Fair Chance Ordinance If you are applying to reputed company work for reputed company in any position which will involve performing at least two (2) hours of work on average each week reputed company the unincorporated areas o

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