Operations Manager Clinical Regulatory Writing

Regulatory Clinical Trial Application Submission ManagerRegulatory Clinical Trial Application Submission ManagerDuties: Manages regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious...

Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...

Regulatory Clinical Trial Application Submission Manager Zabki, Masovian Voivodeship Duties:Managesregulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease)Ensures that the...

Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...

Duties:Managesregulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease)Ensures that the required regulatory intelligence is in place to comply with country-specific requirements...

Do you want to be part of a dynamic team, working in an international environment that drives clinical trial activities? Do you want to develop further as a people manager within the clinical trials field? Then keep reading - we may have just the right job for you Clinical Development Centre (CDC) Poland is expanding and is looking for a new Clinical...

The Clinical Transparency & Data Sharing team is within CMO office and leads the AstraZeneca Group of Companies, Clinical Trial Transparency Position Globally. We are responsible for clinical data sharing, clinical document sharing and clinical transparency patient engagement activities such as the Lay Summaries and Thank you cards. The CTT Anonymization...

Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic focus on...

equire anassociated Typical Accountabilities and required competencies Create Anonymized Clinical Documents following best practices and established SOPs. Contribute to the Anonymization Report for the reports created. Be a system expert in the use of Technology Tool for delivery of Anonymized Clinical Documents. Perform System User Acceptance...

Do you want to be part of a dynamic team, working in an international environment that drives clinical trial activities? Do you want to develop further as a people manager within the clinical trials field? Then keep reading - we may have just the right job for you Clinical Development Centre (CDC) Poland is expanding and is looking for a new Clinical...

As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute, manage and monitor regional, single modality or therapeutic area clinical research projects. Utilizing existing templates, processes and programs as a guide, he or she will adapt/develop, implement, monitor and be accountable for project protocols, operational...

Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular,...

Job DescriptionThis position plays a key role in managing the performance and project execution of assigned protocols in a specific country while ensuring compliance with regulations and company standards.The Clinical Research Manager (CRM) may oversee studies across multiple countries within a cluster.Responsibilities include:Acting as the Main Point of...

Job DescriptionThis position plays a key role in managing the performance and project execution of assigned protocols in a specific country while ensuring compliance with regulations and company standards.The Clinical Research Manager (CRM) may oversee studies across multiple countries within a cluster.Responsibilities include:Acting as the Main Point of...

At AstraZeneca, we are committed to pioneering scientific advancements that revolutionize cancer treatment and positively impact the lives of patients. Our Oncology division is dedicated to eradicating cancer fatalities through cutting-edge research and development. Join us in our mission to drive innovation and shape the future of cancer care. ...

Job Description At PSI, Proposal Manager coordinates all phases of PSI's proposal process while maintaining the company's win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks. You will partner with global teams of subject matter experts from Feasibility, Medical Affairs, Project Management, Clinical...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a...

Hobson Prior is seeking a Senior Manager for Regulatory Operations. This role will be the primary contact for Regulatory Affairs in business projects that involve or impact data, systems, and processes. The successful candidate will ensure data compliance, accuracy, and usability, and will also provide support and training for the relevant community. This...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...