Regulatory Affairs Manager

Join our TeamPlanet Pharma is looking for a skilled professional to fill the role of Regulatory Affairs Manager. As a key member of our team, you will support scientific publications, trial process and compliance. This position offers a great opportunity for growth and development in a dynamic environment.Responsibilities• Manage trial process and...

At Planet Pharma, we are looking for a Regulatory Affairs Specialist to join our team. In this role, you will be responsible for supporting the scientific support and trial process for our client, a leading global pharmaceutical company.Estimated salary: £52,000 per year (dependent on location)Job Overview:The successful candidate will be responsible for...

About UsLloyds Banking Group is committed to creating an inclusive and diverse workplace where everyone feels valued and empowered to succeed. As a global financial services provider, we strive to make a positive impact on customers, businesses, and communities.We are looking for a talented Personal Support Officer to join our Litigation and Regulatory...

About the RoleWe are seeking an experienced Project Coordinator to join our team at Planet Pharma. In this critical position, you will provide crucial support to the Project Manager in managing clinical trials, ensuring that all processes run smoothly and efficiently.Your primary responsibilities will include coordinating the engagement with regulatory...

Key ResponsibilitiesIn this challenging and rewarding role as a Regulatory Affairs Specialist, you will be responsible for ensuring that our client's pharmaceutical products comply with regulatory requirements. Your primary duties will include:Coordinating the submission of scientific publications and postersSupporting the team in engaging with regulatory...

Scientific Support OpportunityWe are seeking a talented individual to join our team as a Clinical Trial Specialist. In this role, you will support scientific support, trial process and compliance at Planet Pharma. With a strong background in life sciences and project management, you will drive digital health technologies and regulatory affairs forward.Key...

Job DescriptionAs a highly skilled Project Manager at Planet Pharma, you will play a vital role in supporting the scientific process and trial compliance for our client, a leading global pharmaceutical company.The successful candidate will be responsible for coordinating the submission of scientific publications, including posters and peer-reviewed articles,...

We are seeking a Senior Clinical Trial Manager to join our team at Planet Pharma. In this role, you will be responsible for supporting the scientific support and trial process for our client, a leading global pharmaceutical company.Estimated salary: £55,000 per year (dependent on location)Job Description:The successful candidate will be responsible for...

Aimée Willow Connex seeks a seasoned Compliance Risk Manager to oversee the firm's compliance framework, ensuring adherence to regulatory requirements and fostering a positive compliance culture. Job Description:We are looking for a highly experienced professional with extensive knowledge of the relevant regulatory landscape, particularly FSMA, CCA, and FCA...

We have an exciting opportunity for a Corporate Affairs Director to join our team at the Countess of Chester Hospital NHS Foundation Trust. As a key member of the senior management team, you will play a critical role in ensuring the Trust's governance structure is fit for purpose.About the TrustThe Countess of Chester Hospital NHS Foundation Trust provides...

Our pharmaceutical client seeks a talented Project Manager for a 12-month contract with the opportunity to extend.Key Responsibilities:Draft and coordinate submission of scientific publications, including posters and peer-reviewed articlesSupport engagement with regulatory agenciesCreate presentations and figures/visualsSustain trial process and...

About the Role:This User Acceptance Testing (UAT) Professional role is part of our Transaction Reporting team based in Chester. As a key member of our team, you will be responsible for ensuring the smooth execution of UAT for large change operations regulatory change programs. This involves working closely with teams across multiple locations, including...

Job OverviewA highly skilled Project Coordinator is sought to support scientific publications, trial process and compliance at Planet Pharma. This 12-month contract offers long-term opportunities for a Life-science graduate with project management experience in the public or private sector.About the RoleThe ideal candidate will have strong digital...

Job DescriptionWe are seeking a Senior Benefits Operations Expert to join our team in Chester, UK. This is an initial 12-month contract on a 50/50 hybrid basis.Key Responsibilities:End-to-end management of benefits programmes.Effective communication of benefit plan provisions and processes to staff.Documentation of all processes and activities.Implementation...

About the RoleAs a Regulatory Assurance Specialist at IDEX Consulting, you will play a vital role in ensuring regulatory excellence and compliance within our advisory operations. With a strong focus on integrity and accountability, this position is ideal for those who are motivated by driving results and shaping future standards in financial planning.Key...

About the RoleWe are looking for a highly skilled Regulatory Affairs Specialist to join our team in Chester. As a key member of our engineering team, you will be responsible for ensuring that all products meet the necessary regulatory standards.Salary: Up to £55,000 + BenefitsThe successful candidate will have a strong understanding of regulatory standards...

About the Role:The Transaction Reporting Specialist will be responsible for designing, preparing, executing, and closing UAT for large change operations regulatory change programs. This role requires strong analytical and problem-solving skills, as well as the ability to work effectively in a team environment. You should have a deep understanding of Global...

About the JobWe are seeking an experienced Senior Benefits Operations Specialist to join our team in Chester. This is an exciting opportunity to work with a leading client, executing the administration of their benefits and retirement program.The successful candidate will be responsible for ensuring the effective end-to-end operation of benefits programs for...

Job DescriptionWe are seeking a highly skilled Regulatory Reporting Operations Professional to join our team in Chester. This role will involve engagement on key issues relating to GTT Controls with various stakeholders, including the Business, Internal & External Audit, Legal, Compliance, Enterprise Testing, and others.The successful candidate will have...

EA Technology is at the forefront of designing and manufacturing LV monitoring and fault restoration products, supporting Electricity Distribution Network Operators (DNOs) as they transition to Net Zero.About the Role:Ensure product compliance with mandatory approvals and legislative standards across relevant regions, including FCC, UL, CE, LVD, EMC, RoHS,...