Lead Biostatistician - FSP

Thermo Fisher Scientific • Cambridge, MA

66d • $107,000 - $162,000

About The Position

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Location/Division Specific Information Our client, a global mid-sized biotech company, focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing, international organization has a strong scientific foundation. If you're looking for a place where your work, in partnership with others, can have real impact—and where you're encouraged to challenge yourself and contribute to breakthrough solutions, the Lead Biostatistician could be a great fit. Please note that candidates must be East-coast based in the United States with flexibility to travel. Extensive study design and sponsor experience required. Your role: You 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. You 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 You will report to a franchise team leader, within the Biostatistics and Statistical Modelling organisation You will carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements

Requirements

• 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)
• 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

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.
• Closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissions
• Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements

Benefits

• We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
• Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.
• We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees