CK Group are recruiting for a Clinical Affairs Specialist on behalf of a medical diagnostic company. This role will be based at their site in Gateshead and is a permanent role with Mon-Fri day time working hours.
Role: This position will be responsible for ensuring thatproducts and training materials are developed and maintained in line with current medical analytical and regulatory guidelines.
Job Specification Responsibilities:- Develop an in-depth technical understanding and expert knowledge of the clinical use of the entire product range.
- Promote the distribution of clinical knowledge throughout the company.
- Perform and maintain comprehensive literature reviews for entire product range.
- Generate and maintain IVDR compliant technical documentation.
- Produce maintain and curate technical training materials.
- Take ownership of predefined projects such as clinical studies and development projects.
- Provide occasional onsite support at customer sites in the UK and internationally.
Your Background:- Educated to degree level or above in Biomedical and Biological Sciences with an understanding of In Vitro Diagnostics and how they affect patient care.
- Experience in a field such as Medical writing Risk assessment training diagnostics laboratory IVDR ISO15189 or ISO13485 or Medical Statistics.
- The ability to produce high quality technical documentation is essential.
- Excellent presentation skills.
- Ability to have high level technical conversations and convey a clear message to a range of healthcare professionals and business colleagues.
- Self-motivated with excellent time management and organisational skills.
Apply: For more information or to apply for this Clinical Affairs Specialist position please contact Mary Bolt on . Please quote job reference 159073 in all correspondence.
It is essential that applicants hold entitlement to work in the UK.
CK Group are recruiting for a Clinical Affairs Specialist on behalf of a medical diagnostic company. This role will be based at their site in Gateshead and is a permanent role with Mon-Fri day time working hours. Role: This position will be responsible for ensuring thatproducts and training material...
CK Group are recruiting for a Clinical Affairs Specialist on behalf of a medical diagnostic company. This role will be based at their site in Gateshead and is a permanent role with Mon-Fri day time working hours.
Role: This position will be responsible for ensuring thatproducts and training materials are developed and maintained in line with current medical analytical and regulatory guidelines.
Job Specification Responsibilities:- Develop an in-depth technical understanding and expert knowledge of the clinical use of the entire product range.
- Promote the distribution of clinical knowledge throughout the company.
- Perform and maintain comprehensive literature reviews for entire product range.
- Generate and maintain IVDR compliant technical documentation.
- Produce maintain and curate technical training materials.
- Take ownership of predefined projects such as clinical studies and development projects.
- Provide occasional onsite support at customer sites in the UK and internationally.
Your Background:- Educated to degree level or above in Biomedical and Biological Sciences with an understanding of In Vitro Diagnostics and how they affect patient care.
- Experience in a field such as Medical writing Risk assessment training diagnostics laboratory IVDR ISO15189 or ISO13485 or Medical Statistics.
- The ability to produce high quality technical documentation is essential.
- Excellent presentation skills.
- Ability to have high level technical conversations and convey a clear message to a range of healthcare professionals and business colleagues.
- Self-motivated with excellent time management and organisational skills.
Apply: For more information or to apply for this Clinical Affairs Specialist position please contact Mary Bolt on . Please quote job reference 159073 in all correspondence.
It is essential that applicants hold entitlement to work in the UK.
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