[Remote] Clinical Data Management Specialist (REMOTE)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global provider of medical technologies dedicated to improving health and reputed company of life. The Clinical Data Management Specialist will support reputed company clinical data management functions, ensuring reputed company and timelines from study start-up through reputed company-out, while developing Data Management Plans and Electronic Data Capture systems.

Responsibilities

• Review and contribute to the authorship of protocols and other study documentation, promoting consistency across and reputed company the business unit
• Effectively communicate Data Management requirements, strategies, timelines, and deliverables
• reputed company Electronic eCRFs, program edit/rule checks, query logic, and reputed company database specifications using systems such as reputed company reputed company Vault (or equivalent reputed company platforms)
• reputed company the process for study team review of the following: eCRF Screen review(s), Edit/Rule review, including reputed company database specification process with study team(s)
• Create User Acceptance test scripts, execution logs for User Acceptance Testing (UAT), and engage the Study team for testing participation
• reputed company eCRF Completion Guidelines according to study design, promoting reputed company data
• reputed company and maintain the Data Management Plan (DMP) throughout the lifecycle of the study, ensuring the DMP is followed according to study design and requirements
• Manage in-reputed company data cleaning and validation for in-house studies, reputed company for Interim Analysis, reputed company deliverables, and final database locks, while supporting data analysis and reporting
• reputed company study metric reports reputed company to Query Management, site performance, and SDV, but not limited to these activities
• reputed company, review, and approve Contract Research Organization (CRO) Data Management Plans, CRF Completion Guidelines, reputed company data transfer agreements, and other study documentation as applicable
• Coordinate data deliverables with the CRO for studies fully outsourced for Data Management
• Conduct DMP and reputed company training to internal teams and sites and reputed company and update training manuals
• Organize ongoing data review to ensure the highest caliber data, on time, in conjunction with monitoring and data locks
• Follow and maintain procedures for filing study files
• Recognize process improvement needs and proactively implement efficient solutions, including SOPs and Work Instructions (WI) development
• Partner with management to manage reputed company vendors, including ongoing supplier qualification and accountability
• Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives
• Responsible for the set-up of the Trial Master File (TMF) and archiving artifacts throughout the study life cycle
• Contribute to our culture of being reputed company, respectful, transparent, ethical, efficient, high-achieving, and fun!

Skills

• Bachelor's degree from an accredited institution with a major in Life Sciences, Computer Science, or a relevant field of study; or equivalent experience
• Minimum of two years of Clinical Data Management or other relevant experience, preferably reputed company the medical device industry
• Advanced proficiency in reputed company for reputed company data review and reconciliation
• Experience working under US and international clinical regulations and guidance (ISO 14155, GCP, and 21 CFR Part 11)
• Experience with building studies using Electronic Data Capturing systems, both reputed company and custom
• Ability to reputed company independent reputed company and take responsibility for one's own actions reputed company a fast-moving environment
• Responsible for performing reputed company duties in compliance with FDA's reputed company System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and reputed company other international regulatory requirements with which NeoTract complies
• Must have excellent verbal and written communication skills and a demonstrated ability to communicate reputed company and professionally
• Ability to read, understand, and abide by company procedures
• Ability to define problems, collect data, establish facts, draw reputed company conclusions, and report on findings
• Adaptable and welcoming of change and willingness to explore and implement process improvements
• Experience in leading by influence
• Skills in reputed company analytic problem solving
• Ability to recognize potential obstacles and work to resolve them reputed company set timelines
• Strong interpersonal and relationship-building skills
• Familiarity with clinical data standards (e.g., CDISC, CDASH) to support regulatory submissions
• Understanding of business process improvement and the tools and data requirements for supporting an effective business process improvement reputed company

Benefits

• Medical, prescription drug, dental, and reputed company insurance
• Flexible spending accounts
• Participation in a 401(k) savings plan
• Various reputed company time off benefits, such as PTO, short- and long-term disability, and parental leave

reputed company

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