Post Market Surveillance Analyst
other jobs Park Street People
Added before 5 Days
- England,South East,Surrey,Epsom and Ewell
- Full Time, Permanent
- Competitive salary
Job Description:
Our client, an innovative company in their field is currently looking for a Post Market Surveillance Analyst to join their team on a full time, permanent basis.
This is a key clinical role supporting the ongoing safety, performance and compliance of the medical device portfolio.
Key Responsibilities
*Collecting, analysing and trending global PMS and PMCF data (complaints, adverse events, feedback, literature) and presenting clear insights to internal stakeholders
*Developing, maintaining and improving clinical documentation including PSURs, study protocols, reports, clinical evaluations and technical file content
*Supporting vigilance and risk management activities, including regulatory reporting, health hazard evaluations and benefit-risk assessments
*Working directly with CROs, distributors and internal teams to ensure compliant, high-quality clinical data collection
Requirements
*Hands-on experience with Post-Market Surveillance and PMCF in the medical device industry
*Proven background in clinical documentation (protocols, study reports, regulatory clinical files)
*Experience working with CROs, databases and clinical data collection systems
*Strong MS Office skills, particularly Excel and Word, with the ability to present data clearly
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
This is a key clinical role supporting the ongoing safety, performance and compliance of the medical device portfolio.
Key Responsibilities
*Collecting, analysing and trending global PMS and PMCF data (complaints, adverse events, feedback, literature) and presenting clear insights to internal stakeholders
*Developing, maintaining and improving clinical documentation including PSURs, study protocols, reports, clinical evaluations and technical file content
*Supporting vigilance and risk management activities, including regulatory reporting, health hazard evaluations and benefit-risk assessments
*Working directly with CROs, distributors and internal teams to ensure compliant, high-quality clinical data collection
Requirements
*Hands-on experience with Post-Market Surveillance and PMCF in the medical device industry
*Proven background in clinical documentation (protocols, study reports, regulatory clinical files)
*Experience working with CROs, databases and clinical data collection systems
*Strong MS Office skills, particularly Excel and Word, with the ability to present data clearly
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Job number 3361880
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Company Details:
Park Street People
Company size: 10–19 employees
Industry: Recruitment Consultancy
Park Street People is one of the Thames Valley’s longest-running recruitment consultancies. We have more than 25 years’? experience recrui...