Are you a detail-driven scientific writer with a passion for turning complex clinical data into clear, compelling evidence? We're partnering with a forward-thinking medical devices company to find a Clinical Evaluation Writer who will play a pivotal role in supporting regulatory success and patient safety across a diverse portfolio on a 6 month contract. As a Clinical Evaluation Writer, you'll take ownership of developing and maintaining key clinical and regulatory documentation. You'll analyse global clinical data, interpret findings, and translate them into robust, compliant reports that support product lifecycle management. Key Responsibilities Collect, review, and interpret clinical data from a range of post-market and clinical follow-up sources Produce and maintain Clinical Evaluation Reports and associated documentation Manage timelines for ongoing updates across multiple devices Develop and refine Clinical Evaluation Plans and safety/performance summaries Collaborate with cross-functional teams to identify evidence gaps and support follow-up strategies Contribute to Post-Market Surveillance and Post-Market Clinical Follow-Up activities Requirements Proven experience writing Clinical Evaluation Reports for medical devices Strong ability to interpret and present clinical data clearly and effectively Solid understanding of clinical evaluation processes and regulatory expectations Experience critically reviewing scientific literature Confident working independently while collaborating across teams Strong organisational skills with the ability to manage competing priorities Proficiency in Microsoft Word and Excel 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.
Mar 19, 2026
Contractor
Are you a detail-driven scientific writer with a passion for turning complex clinical data into clear, compelling evidence? We're partnering with a forward-thinking medical devices company to find a Clinical Evaluation Writer who will play a pivotal role in supporting regulatory success and patient safety across a diverse portfolio on a 6 month contract. As a Clinical Evaluation Writer, you'll take ownership of developing and maintaining key clinical and regulatory documentation. You'll analyse global clinical data, interpret findings, and translate them into robust, compliant reports that support product lifecycle management. Key Responsibilities Collect, review, and interpret clinical data from a range of post-market and clinical follow-up sources Produce and maintain Clinical Evaluation Reports and associated documentation Manage timelines for ongoing updates across multiple devices Develop and refine Clinical Evaluation Plans and safety/performance summaries Collaborate with cross-functional teams to identify evidence gaps and support follow-up strategies Contribute to Post-Market Surveillance and Post-Market Clinical Follow-Up activities Requirements Proven experience writing Clinical Evaluation Reports for medical devices Strong ability to interpret and present clinical data clearly and effectively Solid understanding of clinical evaluation processes and regulatory expectations Experience critically reviewing scientific literature Confident working independently while collaborating across teams Strong organisational skills with the ability to manage competing priorities Proficiency in Microsoft Word and Excel 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.
Our client, a global pharmaceutical company, is currently looking for a Payroll Analyst to join their team in Chester on a full time, 6-month temporary basis (35 hours per week - hybrid working). As a Payroll Analyst, you will be responsible for the end-to-end processing of payroll for the UK region. This is a great opportunity to build your experience within an international business. Key Responsibilities Oversee payroll processes for the UK region including timesheet management, setting up new employees on the system, pay processing and reports in a timely and efficient manner Manage payroll data relating to any tax changes, bonuses and statutory payments Resolve payroll queries that may rise whilst maintaining excellent customer service Liaise with HR and Finance departments to ensure payroll is run efficiently Requirements Previous experience in processing end-to-end payroll particularly within a shared services environment Knowledge of UK payroll as well as their legislation is desirable Great understanding of payroll systems is highly advantageous Experience with Workday and SAP Highly organised and detailed oriented individual with excellent communication skills Park Street People Ltd does not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and complies with all relevant UK legislation. We are acting as an Employment Business in relation to this role.
Oct 09, 2025
Seasonal
Our client, a global pharmaceutical company, is currently looking for a Payroll Analyst to join their team in Chester on a full time, 6-month temporary basis (35 hours per week - hybrid working). As a Payroll Analyst, you will be responsible for the end-to-end processing of payroll for the UK region. This is a great opportunity to build your experience within an international business. Key Responsibilities Oversee payroll processes for the UK region including timesheet management, setting up new employees on the system, pay processing and reports in a timely and efficient manner Manage payroll data relating to any tax changes, bonuses and statutory payments Resolve payroll queries that may rise whilst maintaining excellent customer service Liaise with HR and Finance departments to ensure payroll is run efficiently Requirements Previous experience in processing end-to-end payroll particularly within a shared services environment Knowledge of UK payroll as well as their legislation is desirable Great understanding of payroll systems is highly advantageous Experience with Workday and SAP Highly organised and detailed oriented individual with excellent communication skills Park Street People Ltd does not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and complies with all relevant UK legislation. We are acting as an Employment Business in relation to this role.
Are you passionate about regulatory affairs and eager to help life-changing medical products reach the market? Our client is looking for a Regulatory Affairs Officer to support their team in guiding pharmaceutical, medical device, cosmetics and life sciences companies through complex regulatory landscapes. Whilst part of a team, you will work independently. Aside from regulatory submissions, you will engage with clients providing regular updates and advice on projects. This is a great opportunity to further develop your regulatory knowledge and consulting skills. Key Responsibilities Assist in preparing and submitting regulatory documents for UK, EU and US markets mainly on medical devices Support clinical trial processes, registries and Post-Market Clinical Follow-up studies Research evolving regulatory frameworks to keep strategies cutting-edge Provide updates, presentations and regular communication with clients across multiple time lines Work alongside senior consultants to develop tailored compliance solutions Requirements A degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related field An understanding of clinical trials, registries, and PMCF requirements Experience liaising with regulatory authorities and clients and presenting detailed reports to them Familiarity with global regulatory bodies and frameworks Strong IT skills and attention to detail Excellent communication and problem-solving abilities 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.
Oct 06, 2025
Full time
Are you passionate about regulatory affairs and eager to help life-changing medical products reach the market? Our client is looking for a Regulatory Affairs Officer to support their team in guiding pharmaceutical, medical device, cosmetics and life sciences companies through complex regulatory landscapes. Whilst part of a team, you will work independently. Aside from regulatory submissions, you will engage with clients providing regular updates and advice on projects. This is a great opportunity to further develop your regulatory knowledge and consulting skills. Key Responsibilities Assist in preparing and submitting regulatory documents for UK, EU and US markets mainly on medical devices Support clinical trial processes, registries and Post-Market Clinical Follow-up studies Research evolving regulatory frameworks to keep strategies cutting-edge Provide updates, presentations and regular communication with clients across multiple time lines Work alongside senior consultants to develop tailored compliance solutions Requirements A degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related field An understanding of clinical trials, registries, and PMCF requirements Experience liaising with regulatory authorities and clients and presenting detailed reports to them Familiarity with global regulatory bodies and frameworks Strong IT skills and attention to detail Excellent communication and problem-solving abilities 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.
