Clinical Research Associate (REMOTE)

Expected Travel : Up to 25%

Requisition ID : 12473

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of peoples 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, QuikClot, LMA, Pilling, Rusch, 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 offers innovative medical devices that are used to diagnose and treat coronary and peripheral vascular diseases. We place a strategic emphasis on complex coronary and peripheral interventions, vascular access, bone access, specialty biologic treatments and cardiac assist. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner and Turnpike Catheters, AC3 Optimus Intra-Aortic Balloon Pump and OnControl Powered Bone Access System. With a strong R&D footprint and pipeline, our fast-growing Interventional business unit is poised to continue the development of new technologies to serve critically ill patients for years to come. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients lives.

The Clinical Research Associate (CRA) facilitates clinical investigations, builds relationships, and communicates results. Responsibilities span all phases of clinical studies, including initiation, enrollment, data analysis, and closure.
The CRA designs case report forms, monitoring plans, and study documents; manages data; performs monitoring; maintains study files; and supports site coordinators and investigators. They ensure compliance with regulations and policies, mentor junior staff, and lead projects.

Manage sites from start-up to closure.
Identify and resolve logistical and operational issues.
Conduct site training.
Perform on-site, remote, and centralized monitoring.
Assist with protocol design and data collection methods.
Develop and review essential study documents.
Ensure compliance with FDA and Teleflex requirements.
Oversee in-house study files and audit for compliance.
Assist with IRB submissions and renewals.
Maintain professional relationships with investigators and sites.
Recognize and resolve data discrepancies and compliance issues.
Report serious compliance issues and implement corrective actions.
Review data for completeness and accuracy.
Assist in writing FDA submissions and clinical reports.
Develop and implement study-specific databases.
Support study operations and communication with committees.
Provide input for new projects and departmental policies.
Anticipate and address study conduct issues.
Create and resolve queries and action items.
Complete and review Monitoring Visit Reports and Follow-up Letters.
Support team members in other trials.
Adhere to departmental SOPs and escalate discrepancies.

Bachelor's or Graduate degree in life sciences, nursing or other health related disciplines.
Minimum five years as a CRA in the medical device or pharmaceutical industry or with a CRO.

Demonstrated aptitude and knowledge in relevant therapeutic area (Electrophysiology, Vascular Interventional Cardiology and Neuromodulation) and ability to learn and integrate new or different therapeutic areas.
Strong working knowledge, understanding and ability to apply FDA regulations and ICH/GCP guidelines governing clinical trials.
Current certification as a Certified Clinical Research Associate (CCRA) or current Certified Clinical Research Professional (CCRP) is preferred.
Demonstrated ability to independently lead study or department projects
Demonstrated ability to maintain composure in difficult circumstances and to identify and adapt to shifting priorities and competing demands.
High attention to detail and accuracy.
Proficient knowledge of medical terminology.
Excellent time management and organizational skills.
Excellent professional writing and oral communication skills.
Excellent interpersonal skills.
Ability to work independently as well as part of a team.
Experience with word processing, spreadsheets, and databases applications (e.g., MS Word and Excel)
Ability to lift 25 or more pounds.

TRAVEL REQUIRED: 25%

The pay range for this position at commencement of employment is expected to be between $105,000- $115,000 however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired, employee will be in an at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

#LI-LM1

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 Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: ... or ....

Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rusch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
2025 Teleflex Incorporated. All rights reserved.