Clinical Data Manager

Teleflex; Zürich; Hybrid; CHF 110.000 - 140.000; Vollzeit

Benefits dieser Stelle

Flexible working hours

Mobile Working up to 40%

25 days holidays

Paid absence day on Ascension Friday

Training and development opportunities

Company canteen with options

Public transport discounts / parking

Zusammenfassung

Teleflex Incorporated in Switzerland is seeking a Clinical Data Management Specialist to support data management from start-up through close-out, ensuring high-quality data on time. You will develop and validate DMPs and drive EDC initiatives with a focus on regulatory standards.

The role requires knowledge of CDISC/SDTM, SAS programming, and collaboration within a fast-paced environment. Fluency in English and willingness to learn German are valued assets.

Qualifikationen

• Master’s degree preferred in medicine, life sciences, natural sciences, mathematics or computer science.
• Bachelor’s degree acceptable with relevant experience.
• 2–3 years of professional experience in clinical data management.
• CDISC/SDTM implementation is an advantage.
• GCP, ISO 14155, MDR and 21 CFR Part 11 compliance knowledge is required.
• Fluent in written and spoken English; basic German is a plus.

Aufgaben

• Review study protocols and contribute to documentation for consistency.
• Develop and maintain electronic CRFs and edit/rule checks in EDC.
• Implement CDISC/SDTM standards for data consistency and compliance.
• Perform validation tasks using SAS programming and data processing.
• Create UAT scripts and coordinate testing with study teams.
• Develop Data Management Plans and CDISC-compliant guidelines.
• Oversee data cleaning, validation, and data delivery milestones.
• Produce study metric reports on query management and SDV.

Kenntnisse

Fluent English

Ausbildung

Master’s degree preferred

Bachelor’s degree acceptable

Tools

SAS

SQL

R

Python

Jobbeschreibung

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.

Expected Travel: None

Requisition ID: 14183

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.

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 business unit(s).
• Develop Electronic eCRFs, program edit/rule checks, query logic and generate database specifications using EDC.
• Implements CDISC/SDTM standards within eCRFs to ensure compliance and data consistency.
• Performs additional validation or data processing tasks using SAS programming.
• 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, validation, for in-house studies, accounting for Interim Analysis, abstract deliverables, 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 Data Management Plans, CRF Completion Guidelines, external data transfer agreements and other study documentation as applicable.
• 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.
• Conducts regular reviews of clinical trial data in conjunction with monitoring teams and ensures compliance with GCP, 21 CFR Part 11, ISO 14155, and MDR requirements.

Education / Experience Requirements

• Master’s degree preferred (e.g., in medicine, life sciences, natural sciences, mathematics, or computer science); Bachelor’s degree acceptable with relevant experience.
• Two to three years of professional experience in clinical data management or a closely related field.
• Proficiency in CDISC/SDTM implementation (is an advantage).
• Programming knowledge in SAS, with working knowledge of SQL, R, and Python (is an advantage).
• Experience developing and maintaining data validation plans and documentation.
• Strong understanding of GCP, ISO 14155, MDR and 21 CFR Part 11 compliance (required)
• Fluent in written and spoken English, basic proficiency in German is considered as a plus.

What We Offer

• Flexible working hours
• Mobile Working up to 40%
• At least 25 days of holidays
• Friday after Ascension is a paid absence day
• Training and further development opportunities
• Company canteen with various options
• Discounts for public transportation or affordable parking options

Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.

If you require accommodation and support to apply for a position, please contact us at [e-mail]

Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, QuikClot™, LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.

© 2026 Teleflex Incorporated. All rights reserved.