Clinical Research Scientist (MDR)
- Recruiter
- Hobson Prior
- Location
- United Kingdom
- Salary
- Competitive
- Posted
- 21 Jun 2022
- Closes
- 08 Jul 2022
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Hobson Prior are looking for a Clinical Research Scientist (MDR) to join a brilliant pharmaceutical corporation on a contract basis. Our client is focused on producing a healthier community.
Please note that to be considered for this role you must have the right to work in this location.
*Key Responsibilities: *
* For this role, you will be responsible for analysing briefs of clinical evidence and PMCF methods in any other areas of the technical documents for precision and accomplishment.
* You will uphold a comprehension of developing post-market evidence needs under the EU medical device guidelines.
* To obtain contributions into study design, review study viability, and recognise sites for study implementation or data gathering, you will nurture relations with surgeons, hospitals and research teams when needed.
* To guarantee implementation of all study arrangements in a timely manner and consistent payments for completed indicators and deliverables, you will collaborate with contracts and payments team.
* The ideal candidate will enable clinical evidence evaluations with cross functional teams to be in line with clinical evidence methods, papers / track verdicts and hazards, and scribe PMCF plans.
* Accountable for evolving and scribing high quality post-market clinical follow-up (PMCF) plans and documents while under minimal observation.
* Any other assigned duties.
*Requirements:*
* Educated to a degree level in a biological science or similar field, with at least 4 years of experience within a medical device or healthcare organisation.
* Technical writing abilities, with familiarity with writing PMCF plans and documents.
* Prior involvement operating in the post market stage.
* Acquaintance with end project management with the ability to handle various projects concurrently such as study procedures, regulatory scribing, EUMDR, data assessment, etc.
* Medical devices experience within the spine, neuro, joint and jaw reconstruction divisions.
* Familiarity with evolving methods to produce clinical evidence such as CERs (Clinical Evidence Report).
* Communication abilities both verbally and written.
* Fluency in the English language.
*Apply now*:
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
Please note that to be considered for this role you must have the right to work in this location.
*Key Responsibilities: *
* For this role, you will be responsible for analysing briefs of clinical evidence and PMCF methods in any other areas of the technical documents for precision and accomplishment.
* You will uphold a comprehension of developing post-market evidence needs under the EU medical device guidelines.
* To obtain contributions into study design, review study viability, and recognise sites for study implementation or data gathering, you will nurture relations with surgeons, hospitals and research teams when needed.
* To guarantee implementation of all study arrangements in a timely manner and consistent payments for completed indicators and deliverables, you will collaborate with contracts and payments team.
* The ideal candidate will enable clinical evidence evaluations with cross functional teams to be in line with clinical evidence methods, papers / track verdicts and hazards, and scribe PMCF plans.
* Accountable for evolving and scribing high quality post-market clinical follow-up (PMCF) plans and documents while under minimal observation.
* Any other assigned duties.
*Requirements:*
* Educated to a degree level in a biological science or similar field, with at least 4 years of experience within a medical device or healthcare organisation.
* Technical writing abilities, with familiarity with writing PMCF plans and documents.
* Prior involvement operating in the post market stage.
* Acquaintance with end project management with the ability to handle various projects concurrently such as study procedures, regulatory scribing, EUMDR, data assessment, etc.
* Medical devices experience within the spine, neuro, joint and jaw reconstruction divisions.
* Familiarity with evolving methods to produce clinical evidence such as CERs (Clinical Evidence Report).
* Communication abilities both verbally and written.
* Fluency in the English language.
*Apply now*:
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.