Clinical Specialist – Post-Market Surveillance - Franklin Lakes, New Jersey, United States

This position participates in Post Market Surveillance (PMS) activities with customers.The Clinical Specialist – Post-Market Surveillance associate will demonstrate technical skills in disciplines of clinical laboratory science such as specimen collection, · clinical chemistry, · ...

This role ensures Stryker's medical devices meet the highest standards after they reach the market. You'll drive patient safety and product excellence while influencing global compliance and improving product performance. · Develop and maintain Post Market Surveillance documentat ...

Drive patient safety and product excellence in this remote role ensuring Stryker's medical devices meet the highest standards after they reach the market. · ...

+Job summary · This position participates in Post Market Surveillance (PMS) activities with customers. The Clinical Specialist – Post-Market Surveillance associate will demonstrate technical skills in disciplines of clinical laboratory science such as specimen collection,Addition ...

This position participates in Post Market Surveillance (PMS) activities with customers. · * Conducts customer surveys for BD products following the BD Vacutainer Tube Products Post Market Surveillance Quality Plan.* Report product issues from customers to the BD complaints team a ...

The Market Surveillance Analyst will work with Compliance and Technology teams to design an enterprise surveillance and research repository. · Data Integrity and Monitoring: Responsible for the timely analysis of trade based alerts leading to the detection and prevention of marke ...

The Head of Market Integrity and Surveillance Compliance (Internal Audit) will manage the internal audit activities for OKX's Markets Compliance function. · This role ensures that the organization's risk management and market integrity frameworks are robust, effective, · and alig ...

We are seeking a Head of Market Integrity and Surveillance Compliance (Internal Audit) to manage our internal audit activities for OKX's Markets Compliance function. · Ensure that our risk management and market integrity frameworks are robust, effective, and aligned with regulato ...

The Head of Market Integrity and Surveillance Compliance (Internal Audit) will manage the internal audit activities for OKX's Markets Compliance function. This role ensures that the organization's risk management and market integrity frameworks are robust, effective, · and aligne ...

Manage internal audit activities for OKX's Markets Compliance function to ensure risk management and market integrity frameworks are robust, effective, and aligned with regulatory expectations. · ...

+Job Summary · We are seeking a skilled and detail-oriented Global Post Market Complaint Reporting Specialist to join our Post Market Surveillance team. · +Assess individual complaints for adverse events using sound judgment, product and clinical knowledge · Authors and submits h ...

The Clinical Project Leader (CPL) has the responsibility to define and implement the safety and efficacy (S&E) requirements for current and proposed products. · ...

The Medical Writer in Client Medical Pharmaceutical Systems Medical Affairs is responsible for generating and developing documents relating to Clinical and Human Factors assessments. · Within this role, the Medical Writer will write and update Clinical Development Plans, · Human ...

The Clinical Research Associate (CRA) is responsible for planning, negotiating, conducting, monitoring, and reporting on clinical trials.The CRA is responsible for protocol development, site selection and qualification, preparing Informed Consent materials, contracting, training, ...

The Clinical Project Leader has the responsibility to define and implement the safety and efficacy requirements for current and proposed products. · ...

The Medical Writer in client Medical Pharmaceutical Systems Medical Affairs is responsible for the generation and development of documents relating to Clinical and Human Factors assessments, · evaluations and post market surveillance summaries. The medical writer is a pivotal rol ...

The Associate Director serves as BD's global process owner for the Field Action process. · This position partners with Business Units, Regions, Regulatory Compliance, Post Market Quality,and other functions to ensure consistent application of the global process. · The role streng ...

This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices. · Applies laboratory knowledge to manage complaint testing through design of testing methods. · Provides input ...

This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices. · Possess a technical competence and works with human blood in clinical laboratory disciplines such as phleboto ...

The Associate Director serves as BD's global process owner for the Field Action process. · Maintains process standards · Serves as process expert during audits · ...