Pharma IT Validation and Compliance Professional

IT Compliance Lead with exp in GxP and Pharma preferred The IT Compliance Lead is responsible for defining and executing Validation and qualification strategy for the development and implementation of Genetics Analysis Platform, a Non-GxP SaaS solution, and subsequently another upcoming solution. The IT Validation and Compliance Partner is responsible for...

About the RoleWe are seeking an experienced IT Compliance Lead to develop and implement a validation strategy for our Genetics Analysis Platform.This role requires strong analytical and communication skills, with the ability to deliver high-quality documentation and assess IT risks.The ideal candidate will have experience working in GxP and Pharma...

We are looking for a Regulatory Compliance Lead to join our team at Macure Pharma. As a key member of our Regulatory Affairs department, you will be responsible for ensuring compliance with regulatory requirements and guidelines. Your expertise in eCTD publishing and regulatory submission workflows will be instrumental in shaping our digital regulatory...

Senior / Principal Clinical Project Management Consultants Pharma IT is hiring Senior & Principal Clinical Project Management Consultants to join our Clinical Science & Trial Operations Team In this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries. In this position, you will work on-site at the...

Job OverviewThe IT Compliance Lead is responsible for developing and executing a validation strategy for the Genetics Analysis Platform, a Non-GxP SaaS solution.This role involves delivering end-to-end documentation and performing assessments such as supplier evaluation, IT risk assessment, and functional assessments.The IT Compliance Lead will ensure that...

**Key Responsibilities**As a Senior Clinical Project Management Consultant at Pharma IT, you will be responsible for:Leading the development and execution of clinical projects from initiation to closure.Ensuring adherence to project timelines, budget, and scope.Developing comprehensive project plans, including outsourcing plans, risk management, sponsor...

Job SummaryThe IT Compliance Lead will be responsible for defining and executing a validation strategy for the Genetics Analysis Platform.This role involves working closely with cross-functional teams to deliver high-quality documentation and ensuring system compliance with regulatory requirements.The ideal candidate will have experience working in GxP and...

As a Senior Regulatory Publisher & Submission Manager at Macure Pharma, you will play a key role in shaping regulatory processes and implementing our new Submission Publishing Tool.Your responsibilities will include:Compiling, formatting, and validating regulatory submissions in eCTD.Implementing and optimizing our digital document management system to...

We are seeking an experienced IT Validation and Compliance Partner to join our team at Ubique Systems. In this role, you will be responsible for delivering end-to-end documentation and performing various assessments to ensure the quality and integrity of our systems.About the Role:Develop and implement validation and qualification strategiesWrite and deliver...

**About the Role**We are seeking a highly skilled Clinical Project Manager Consultant to join our team at Pharma IT. As a senior member of our Clinical Science & Trial Operations Team, you will be responsible for leading clinical projects from initiation to closure, ensuring adherence to project timelines, budget, and scope.As a consultant, you will work...

As a Senior Project Manager at Anzurra, you will have the opportunity to work on challenging and rewarding projects in the Pharma industry. You will be responsible for leading a team of PMs to deliver successful projects, while also developing and implementing project plans, ensuring compliance with regulations, and maintaining strong relationships with...

Project Lead Clinical OperationsWe are seeking an experienced Project Lead Clinical Operations to join our Clinical Science & Trial Operations Team at Pharma IT.As a Project Lead Clinical Operations, you will be responsible for leading the development and execution of clinical projects, from initiation to closure, ensuring adherence to project timelines,...

Clinical Project ManagerWe are seeking an experienced Clinical Project Manager to join our Clinical Science & Trial Operations Team at Pharma IT.As a Clinical Project Manager, you will be responsible for managing the development and execution of clinical projects, from initiation to closure, ensuring adherence to project timelines, budget, and scope.Your key...

Principal Clinical Research ManagerAre you looking for a challenging role that combines your clinical expertise with business acumen?We are seeking an experienced Principal Clinical Research Manager to join our Clinical Science & Trial Operations Team at Pharma IT.As a Principal Clinical Research Manager, you will be responsible for leading the development...

Senior Consultant Clinical TrialsPharma IT is a leading provider of clinical project management services to the pharmaceutical, biotechnology, and medical device industries.We are seeking an experienced Senior Consultant Clinical Trials to join our team. As a Senior Consultant Clinical Trials, you will work closely with cross-functional teams to develop and...

This is an exciting opportunity for a seasoned professional to take on a leadership role in our Global Audits & Development Quality team. If you are passionate about quality management and have a proven track record in the pharmaceutical industry, we encourage you to apply.About the ResponsibilitiesDelivering inputs to define the Global Quality business...

Select how often (in days) to receive an alert: Medical Writing and Clinical Disclosure Professional Field of work: Clinical Development Posting Date: 12 Mar 2025 Role Description Are you a skilled professional with a passion for medical writing and clinical disclosure? LEO Pharma is seeking a talented Medical Writing and Clinical Disclosure Professional to...

Macure Pharma is seeking a Publisher & Submission Manager to join our Regulatory Affairs team. In this role, you will be responsible for compiling, formatting, and validating regulatory submissions in eCTD format. You will also play a key role in the implementation of our new Submission Publishing Tool, leveraging your expertise in EDMS systems and workflow...

Job DescriptionThe Compliance Professional will be responsible for designing, implementing, and continuously optimizing best-in-class policies and compliance procedures to comply with regulatory requirements and ethical standards.You will oversee the compliance efforts in AIP, focusing on protecting our business and our employees and maintaining a good...

The IT Compliance Lead will play a key role in ensuring that Ubique Systems' systems are compliant with relevant regulatory requirements. Key responsibilities include developing and implementing a comprehensive validation strategy, coordinating supplier assessments, and ensuring data integrity.About Us:We are a leading provider of Genetics Analysis Platform...