Clinical Data Management Specialist (Remote, MA, US)

About this role

Expected Travel: Up to 10%
Requisition ID: 13976
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Interventional – The Interventional business unit at Teleflex develops innovative medical devices used to diagnose and treat coronary and peripheral vascular diseases. We focus strategically on coronary and peripheral interventions, vascular and bone access, and large-bore closure solutions.
Our portfolio includes a broad range of clinically relevant products, such as the GuideLiner™ and Turnpike™ Catheters; the Orsiro™ Mission™ Drug-Eluting Stent; the PK Papyrus™ Covered Coronary Stent; the Ringer™ Perfusion Balloon Catheter; the Pulsar™ -18 T3 Self-Expanding Stent; Passeo™ Balloon Catheters; and the OnControl™ Powered Bone Access System.
Backed by a strong R&D pipeline, our rapidly growing Interventional business unit is well positioned to continue advancing new technologies that support the treatment of critically ill patients. Join a dynamic team dedicated to delivering innovative medical solutions that make a meaningful difference in patients’ lives.

Position Summary

As an integral member of the Clinical Operations team, the Clinical Data Management Specialist supports all Clinical data management functions within timeline and quality objectives, from study start-up through close-out. With oversight from management, this position partners to develop and execute Data Management Plans (DMPs) and builds and validates Electronic Data Capture (EDC). This position requires strong knowledge of EDC experience in clinical trials and related regulations, and the ability to perform at a high level in a fast-paced, dynamic environment.

Principal Responsibilities

• Review and contribute to the authorship of protocols and other study documentation, promoting consistency across and within the business unit.
• Effectively communicate Data Management requirements, strategies, timelines, and deliverables.
• Develop Electronic eCRFs, program edit/rule checks, query logic, and generate database specifications using systems such as Veeva CDMS Vault (or equivalent EDC platforms).
• Lead the process for study team review of the following: eCRF Screen review(s), Edit/Rule review, including EDC 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.
• Develop eCRF Completion Guidelines according to study design, promoting quality data.
• Develop 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-stream data cleaning and validation for in-house studies, accounting for Interim Analysis, abstract deliverables, and final database locks, while supporting data analysis and reporting.
• Generate study metric reports related to Query Management, site performance, and SDV, but not limited to these activities.
• Oversee, review, and approve Contract Research Organization (CRO) Data Management Plans, CRF Completion Guidelines, external 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 EDC training to internal teams and sites and develop 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 external 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 collaborative, respectful, transparent, ethical, efficient, high-achieving, and fun!

Education / Experience Requirements

• 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 within the medical device industry.
• Advanced proficiency in Excel for complex 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 out-of-the-box and custom.
• Understanding of business process improvement and the tools and data requirements for supporting an effective business process improvement practice.
• Preferred: Familiarity with clinical data standards (e.g., CDISC, CDASH) to support regulatory submissions.

Specialized Skills / Other Requirements

• Ability to make independent decisions and take responsibility for one's own actions within a fast-moving…