Planet Pharma
Overview
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Sr. Biostatistician
role at
Planet Pharma . Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program. Collaborate with program partners and stakeholders to deliver statistical deliverables for one or more clinical trials and contribute to HA submissions. Report to a franchise team leader within the Biostatistics and Statistical Modelling organisation. Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements. Responsibilities
Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program. Collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions. Report to a franchise team leader, within the Biostatistics and Statistical Modelling organisation. Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements. Education And Experience
You have a master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 5 years experience (which may include doctoral research in field of biostatistics) (Master is a required qualification). You have expertise in drug development, with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials. Demonstrates ability to plan, supervise, implement and monitor the statistical processes for multiple clinical trials. You are proficient in statistical software (SAS and/or R). You are able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials. You can clearly explain complex statistical concepts in written and spoken English. You are a team-player with focused attitude. You are able to work autonomously as part of a cross-disciplinary team in a dynamic environment of a fast growing biotech company with challenging timelines. Knowledge, Skills And Abilities
eCRT and Define knowledge Proactive in nature Project Lead abilities – experience of working with cross functional teams and managing TA experience is preferable (Immunology) Exposure to regulatory related work Exposure to latest Stat models and design approaches will be preferred Proactive communication CO/NY candidates may not be considered Equal Employment Opportunity: The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Job Details
Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Staffing and Recruiting Note: The original posting contained references to application timing and other postings. This refined description focuses on the Sr. Biostatistician role and its requirements without duplicative or unrelated content.
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Join to apply for the
Sr. Biostatistician
role at
Planet Pharma . Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program. Collaborate with program partners and stakeholders to deliver statistical deliverables for one or more clinical trials and contribute to HA submissions. Report to a franchise team leader within the Biostatistics and Statistical Modelling organisation. Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements. Responsibilities
Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program. Collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions. Report to a franchise team leader, within the Biostatistics and Statistical Modelling organisation. Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements. Education And Experience
You have a master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 5 years experience (which may include doctoral research in field of biostatistics) (Master is a required qualification). You have expertise in drug development, with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials. Demonstrates ability to plan, supervise, implement and monitor the statistical processes for multiple clinical trials. You are proficient in statistical software (SAS and/or R). You are able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials. You can clearly explain complex statistical concepts in written and spoken English. You are a team-player with focused attitude. You are able to work autonomously as part of a cross-disciplinary team in a dynamic environment of a fast growing biotech company with challenging timelines. Knowledge, Skills And Abilities
eCRT and Define knowledge Proactive in nature Project Lead abilities – experience of working with cross functional teams and managing TA experience is preferable (Immunology) Exposure to regulatory related work Exposure to latest Stat models and design approaches will be preferred Proactive communication CO/NY candidates may not be considered Equal Employment Opportunity: The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Job Details
Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Staffing and Recruiting Note: The original posting contained references to application timing and other postings. This refined description focuses on the Sr. Biostatistician role and its requirements without duplicative or unrelated content.
#J-18808-Ljbffr