Director/ Senior Director, Biostatistics

Cogent Biosciences
Location
Waltham, Massachusetts
Job Type
Full-time
Posted
June 22, 2026
Views
12
Salary Range
$225k - $265k USD

Job Description

Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent’s lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V.

KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling.

Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing.

The Role: The Director/Senior Director of Biostatistics provides scientific and strategic guidance for one or more clinical development projects. In this role, you will ensure the design, analysis, and interpretation of study data meet the highest standards of scientific rigor and regulatory compliance.

You will collaborate closely with partner functions—including Medical, Clinical Science, Clinical Operations, Data Management, and Statistical Programming—to support study objectives, contribute to regulatory submissions, and help drive the success of clinical development programs. This position reports to the VP, Biometrics.

Responsibilities: Serve as statistical lead for assigned oncology clinical programs, providing strategic and hands-on statistical leadership from early development through pivotal trials and regulatory submissions. Provide statistical input into clinical development strategy, protocol design, endpoint selection, estimands, sample size calculations, interim analyses, and adaptive designs.

Develop and review statistical analysis plans, clinical study reports, regulatory documents, and responses to health authority questions. Support NDA/BLA submissions and regulatory interactions with statistical expertise. Oversee statistical activities performed by CROs and external consultants, ensuring high-quality and timely delivery of statistical outputs.

Collaborate closely with Clinical Development, Regulatory Affairs, Data Management, Clinical Operations, and Statistical Programming teams. Contribute to building and enhancing Biometrics capabilities, processes, and best practices in a growing biotech environment.

Qualifications: Ph.D. in Biostatistics or Statistics with at least 8+ years of experience in pharmaceutical or biotechnology industry; or MS with at least 10+ years of relevant experience. Strong oncology clinical development experience preferred. Experience as the lead statistician for one or more clinical development projects, including pivotal studies.

Experience supporting regulatory submissions (NDA/BLA/MAA) and interactions with health authorities. Strong understanding of ICH GCP and general knowledge of industry practices and standards. Proficiency in SAS programming and other statistical software, including EAST, nQuery, or PASS. Experience with CDISC standards, including SDTM, ADaM, CDASH.

Excellent communication, leadership, and cross-functional collaboration skills. Salary Range: Director: $225,000 - $265,000 Sr. Director: $255,000 - $300,000 Target Bonus: Director: 20%, Sr. Director: 25%   Exact compensation will vary based on skills, experience, and location.

Our Locations Waltham, MA: Our  headquarters is located in the Greater  Boston  life sciences   community, with  an open , collaborative office environment designed   to support teamwork and connection.

Employees  benefit  from convenient on-site amenities, including free  on-site parking and gym facilities in the building.   Boulder, CO:  Our Boulder location is home to  Cogent’s  discovery research organization and a key scientific hub with strong leadership  based on site .

Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent’s lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V.

KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling.

Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing.

The Role: The Director/Senior Director of Biostatistics provides scientific and strategic guidance for one or more clinical development projects. In this role, you will ensure the design, analysis, and interpretation of study data meet the highest standards of scientific rigor and regulatory compliance.

You will collaborate closely with partner functions—including Medical, Clinical Science, Clinical Operations, Data Management, and Statistical Programming—to support study objectives, contribute to regulatory submissions, and help drive the success of clinical development programs. This position reports to the VP, Biometrics.

Responsibilities: Serve as statistical lead for assigned oncology clinical programs, providing strategic and hands-on statistical leadership from early development through pivotal trials and regulatory submissions. Provide statistical input into clinical development strategy, protocol design, endpoint selection, estimands, sample size calculations, interim analyses, and adaptive designs.

Develop and review statistical analysis plans, clinical study reports, regulatory documents, and responses to health authority questions. Support NDA/BLA submissions and regulatory interactions with statistical expertise. Oversee statistical activities performed by CROs and external consultants, ensuring high-quality and timely delivery of statistical outputs.

Collaborate closely with Clinical Development, Regulatory Affairs, Data Management, Clinical Operations, and Statistical Programming teams. Contribute to building and enhancing Biometrics capabilities, processes, and best practices in a growing biotech environment.

Qualifications: Ph.D. in Biostatistics or Statistics with at least 8+ years of experience in pharmaceutical or biotechnology industry; or MS with at least 10+ years of relevant experience. Strong oncology clinical development experience preferred. Experience as the lead statistician for one or more clinical development projects, including pivotal studies.

Experience supporting regulatory submissions (NDA/BLA/MAA) and interactions with health authorities. Strong understanding of ICH GCP and general knowledge of industry practices and standards. Proficiency in SAS programming and other statistical software, including EAST, nQuery, or PASS. Experience with CDISC standards, including SDTM, ADaM, CDASH.

Excellent communication, leadership, and cross-functional collaboration skills. Salary Range: Director: $225,000 - $265,000 Sr. Director: $255,000 - $300,000 Target Bonus: Director: 20%, Sr. Director: 25%   Exact compensation will vary based on skills, experience, and location.

Our Locations Waltham, MA: Our  headquarters is located in the Greater  Boston  life sciences   community, with  an open , collaborative office environment designed   to support teamwork and connection.

Employees  benefit  from convenient on-site amenities, including free  on-site parking and gym facilities in the building.   Boulder, CO:  Our Boulder location is home to  Cogent’s  discovery research organization and a key scientific hub with strong leadership  based on site .

Situated in the greater Denver-Boulder  biopharmaceutical corridor , this office plays  a central role  in advancing our discovery efforts and  pipeline .   Our Offer  To  You   At Cogent Biosciences, we offer a competitive salary, bonus, and ongoing stock awards, alongside a benefits package that  se t s us apart .   We cover 100% of medical, dental, and vision premiums for you and your family,  and  help  reduce  out-of-pocket costs by funding up to 75% of in-network deductibles .  Our benefits also include  a 401(k) match with immediate vesting ,  generous paid time off,  12 weeks  of fully paid parental leave, paid  family  and medical leave for all employees regardless of location, and company-paid short-term disability coverage for up to  20 week s .   A dditional   perks  like   wellness  programs, tuition reimbursement, and inclusive family-forming support help you thrive at work and beyond.   We are proud to be an

Equal Opportunity Employer. Our goal is to have a diverse workforce.  We do not discriminate on the basis of race, age, color, religion, national origin, gender, sexual orientation, gender identity or expression, veteran status or disability, or any other status protected under federal, state, or local law.  All employment is decided on the basis of qualifications, merit, and business  need .

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The job is located in Waltham, Massachusetts. The Waltham headquarters features an open, collaborative office environment designed to support teamwork and connection, with on-site amenities like free parking and gym facilities.
Who will I report to in this role?
This position reports directly to the VP, Biometrics.
What are the key responsibilities of this position?
You will serve as the statistical lead for assigned oncology clinical programs, providing strategic and hands-on leadership from early development through regulatory submissions. You will design protocols, develop statistical analysis plans, support NDA/BLA submissions, oversee CRO activities, and collaborate cross-functionally.
What qualifications and experience are required?
You need a Ph.D. in Biostatistics or Statistics with 8+ years of biotech/pharma experience, or an MS with 10+ years of experience. Required skills include leading clinical projects, supporting regulatory submissions, proficiency in SAS and software like EAST/nQuery/PASS, and knowledge of CDISC standards. Oncology experience is preferred.
What is the salary range for this role?
The salary range for the Director level is $225,000 - $265,000 with a 20% target bonus. For the Senior Director level, the range is $255,000 - $300,000 with a 25% target bonus.
What benefits does Cogent Biosciences offer?
Benefits include 100% covered medical, dental, and vision premiums for you and your family, 401(k) match with immediate vesting, generous PTO, 12 weeks of fully paid parental leave, tuition reimbursement, and wellness programs.

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Job Information

Source: builtin
Remote Type: onsite
Allowed Locations: Waltham, Massachusetts
Skills & Tags:
boston biotech

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