REGULATORY CLINICAL STRATEGY SUBMISSIONS jobs in UNITED KINGDOM, United Kingdom #3

regulatory strategy for the UK. Ensuring full regulatory and company compliance, and provide regulatory expertise to support... to licensing, regulatory changes, and submissions to MHRA. Contributing to a Brand Team representing Regulatory Affairs...

to build a true end-to-end gene therapy offering. This includes our pre-clinical centre of excellence and CMC team acquired... motivated and ambitious Strategy Associate to support us in the next phase of our growth journey. In this role, you will work...

are determined to make life better for people around the world. Director/Snr Director - Statistics - HTA Data Strategy Location... most efficient or innovative approach in economic modeling, (network)-meta-analysis and indirect comparisons, clinical trials...

, and monitors the Data Management strategy for one or more clinical studies in Ipsen portfolio. The Study Lead is responsible...Title: Clinical Data Management Study Lead Company: Ipsen Bioscience, Inc. Job Description: Clinical Data...

of our portfolio in oncology and help to define the broader clinical development strategy. You will interface with sites, CROs... to IND, NDA, PMA submissions via overseeing medical documentation and active participation in meetings with regulatory...

clinical sites (including feasibility and site selection), support ethics committee and regulatory submissions, ensuring... to join one of the largest UK Cancer Research Collaboration (UKCRC) registered clinical trials unit in the country. The Cancer Research...

. Successful candidate would also participate in regulatory submissions and response to regulatory queries. The candidate will directly... contribute to Company success by increasing the strength of study designs, interpret-ability of results, regulatory strategy...

are used to support drug applications and regulatory submissions to health authorities globally. Trial Data Management (TDM... and experience in the Clinical Trials domain to help us implement our vision and strategy to enable the software products within the...

. Successful candidate would also participate in regulatory submissions and response to regulatory queries. The candidate will directly... contribute to Company success by increasing the strength of study designs, interpret-ability of results, regulatory strategy...

, CSR and clinical sections of regulatory submissions. Incorporates HEOR requirements into protocol design Presents various..., you will be accountable for designing and conducting a global medical program resulting in quality regulatory submissions and act as the...

agencies (FDA, EMA) to support clinical trial regulatory submissions Liaise with other functions to enable quality clinical..., MA) The Clinical Development Lead will primarily focus on study design strategy for the development of clinical study...

, product specialists, marketing, regulatory and medical, and inputs as required with key wording and collation of clinical... is to educate and support both HCPs and internal teams on clinical aspects of Ostomy care. To support with education from diagnosis...

, product specialists, marketing, regulatory and medical, and inputs as required with key wording and collation of clinical... is to educate and support both HCPs and internal teams on clinical aspects of Ostomy care. To support with education from diagnosis...

adherence to regulatory and ICH GCP requirements. Key Tasks & Accountabilities Reporting into the Head of Clinical Trials... successful delivery of Clinical Trials: Study Set Up Significant input in the development of study design, protocol, and strategy...

U.K.- and U.S.-based biotechnology hub locations. Our comprehensive capabilities and teams include preclinical research, clinical... submissions. The candidate will be expected to design, execute and analyse experiments in the laboratory within a team setting...

U.K.- and U.S.-based biotechnology hub locations. Our comprehensive capabilities and teams include preclinical research, clinical... submissions. The candidate will be expected to design, execute and analyse experiments in the laboratory within a team setting...

submissions ensuring the coordination and integration of the scientific, medical, and regulatory input from development team... members. Implements regulatory documentation standards that support speed and consistency of regulatory submissions...