candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinicaltrials on a global scale. Join our highly.... We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical...
candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinicaltrials on a global scale. Join our highly..., and supervision of clinicaltrials in hemato-oncology. You will contribute to study design, regulatory submissions, data review...
to date on clinicaltrials, both investigator initiated and external studies, that can be used to improve clinical and health economic... with hypertension. The company is focused on investing in high quality product development efforts, as well as rigorous clinical studies...
, creative approaches and implement them with quality and excellence. We are WorldwideClinicalTrials, and we are a global... and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference...
’s project team in the execution of early clinicaltrials. Joining our team offers the opportunity to work on innovative projects... clinicaltrials in early clinical development for both Sponsor and Study site. Support Clinical Trial Leaders, Clinical Trial...
, we are a global innovation leader with more than 300 clinicaltrials across over 20 different cancer types and therapies reaching... paths, and continuously learn. In an international environment and our vibrant culture, over 50,000 employees worldwide...
, we are a global innovation leader with more than 300 clinicaltrials across over 20 different cancer types and therapies reaching... paths, and continuously learn. In an international environment and our vibrant culture, over 50,000 employees worldwide...
that appropriate regulatory requirements for market clearance or clinicaltrials are built into project plans. Developing regulatory..., LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow...
in clinicaltrials, ensuring adherence to regulatory and ethical standards. Plan and conduct internal and external audits... environments (e.g., clinicaltrials) Knowledge of quality standards and regulatory requirements (e.g., ICH GCP, EU GMP...
, and format a wide range of documents (of low to high complexity) required for research, non-clinical, clinical development... in BioNTech-relevant indications. drafting alone new or updated CTPs and CSRs required for Phase I-III trials. drafting low...