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Research Scientist

Michael Bailey Associates - UK Contracts

Posted on Mar 25, 2022 by Michael Bailey Associates - UK Contracts

Zuchwil, Solothurn, Switzerland
Research
1 Apr 2022
Annual Salary
Contract/Project

A medical device company in Switzerland is looking for a Research Scientist to join their clinical trials team for Neurovascular Medical Devices. Below is a list of some requirements and responsibilities. To find out more details do not hesitate to submit your application and we will contact you!

Responsibilities:

- Primary performs the role of Clinical Study Lead, and may perform other roles including Clinical Operations Lead.
- Manage low complexity, non-regulated studies (Investigator Initiated, Registries, or company sponsored Postmarket studies).
- Assist with high complexity or regulated studies (IDE, HDE, Post-Approval, 522), and may manage components.
- Complete required templates and documents, and maintain records related to assigned projects.
- Develops an understanding of the roles and responsibilities of other functional areas including Franchise Clinical Operations, Biostatistics and Data Management, Medical Affairs, Evidence Based Medicine, Regulatory Affairs, Legal, Health Care Compliance, Research and Development, and Marketing.
- Complete clinical tasks related to product development activities; may participate in Project Core Team (PCT).
- Assist in Front End activities related to clinical feasibility, including literature reviews.
- Assist with the development of materials to be used by Clinical Operations for study execution (Investigator Brochures, training materials, etc.).
- Verify milestones and track payments for assigned Operating Company-managed projects.
- Responsible for technical writing, which may include drafting of components of protocols, study reports, reports to regulatory bodies, or summaries of clinical literature.
- Support the implementation of new clinical systems/processes.
- Keep management informed of key developments and issues that impact clinical strategy and portfolio management.
- Ensure the completion of required templates and documents, and maintenance of records.
- Develop high standards of critical thinking, analysis, collaboration, and communication for the advancement of clinical programs.
- Develop an understanding of the Operating Company product portfolio and pipeline.

Requirements:

- BS/BA or equivalent, preferably in Life Sciences, Biomedical Engineering, or related field required.
- Advanced medical science or medical degree is desirable.
- Desirable minimum durations of relevant experience: BSc with 3 years; Masters with 1 year; PhD/MD/PharmD with 0 to 1 year.
- Previous clinical research or related technical experience required.
- Experience with medical devices is desirable.
- Certification from a recognized professional organization (ie, CCRA, RAC, CDE) is desirable
- English Fluent spoken and written; German a strong asset

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

Reference: 1541763570

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