Sr. Biostatistician at Planet Group Massachusetts

Planet Group; Massachusetts; On-site; USD 79,900 - 106,075; Full time

Job summary

Planet Group in Massachusetts is seeking a Sr. Biostatistician to design and analyze clinical trials and contribute to development plans for one or more compounds.

You will collaborate with program partners and stakeholders to deliver statistical deliverables and HA submission support. The role reports to a franchise team leader within Biostatistics and Statistical Modelling and requires strong English communication, teamwork, and autonomous cross-functional collaboration in a fast-growing

Qualifications

• Master's degree in Statistics or related field; PhD acceptable.
• Minimum 5 years experience in biostatistics for clinical trials.
• Proficiency in SAS and/or R.
• Ability to explain complex statistics in written and spoken English.
• Team player with ability to work autonomously in a fast-growing biotech environment.

Responsibilities

• Contribute statistical expertise to design and analysis of clinical trials and development plans.
• Collaborate with program partners to deliver statistical deliverables for trials.
• Report to a franchise team leader within Biostatistics and Statistical Modelling.
• Adhere to applicable company guidelines and regulatory requirements.

Skills

Statistical expertise

Drug development knowledge

Cross-functional collaboration

Project leadership

Regulatory experience

Education

Master's degree in Statistics

PhD in Statistics

Tools

SAS

R

Job description

Sr. Biostatistician – Planet Group, Massachusetts

Job Description

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 organisation.

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 a related field with a minimum of 5 years experience (which may include doctoral research in 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 statistical models and design approaches will be preferred.
• Proactive communication.

Pay Rate Range: $58.20 - $77.46/hr depending on experience.