19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEDiseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced
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