Biostatistician • usa
Location: Remote Cambridge, MA.Duration: 12+ months with potential extension.Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical dev... Show more
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Position Details:
Role: Sr Biostatistician
Location: Remote Cambridge, MA
Duration: 12+ months with potential extension
Description
Role:
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.
Will closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions
Will report to a franchise team leader, within the Biostatistics and Statistical Modelling organization
Will 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 surrounding 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
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Best Regards,
