Job Description

Telecommuting: Telecommuting is available (1-3 days per week required in office location in Cambridge, Massachusetts).

Responsibilities:

1. Function as lead biostatistician for a clinical program and provide technical and business expertise in support of statistical activities;
2. Oversee the day-to-day biostatistics activities, timelines and deliverables for in-house biostatistics as well as outsourced services;
3. Serve as an integral part of clinical study and program team and contribute to clinical protocol development, statistical analysis plans, and clinical study reports;
4. Apply statistical expertise to ensure optimal complex and innovative clinical trial designs, analysis methods and data displays;
5. Ensure scientific integrity of statistical methodology applied to clinical studies;
6. Collaborate with other functional areas within the company (Clinical Operations, Clinical Research & Development, Clinical Pharmacology, Translational Medicine, Clinical Data Management, Pharmacovigilance, Regulatory and Project Management);
7. Lead and support the planning and preparation of regulatory submissions: briefing books and integrated summary documents;
8. Support the presentation and publication of clinical trial results and contribution to advances on statistical topics and present at scientific conferences; and
9. Help develop department Standard Operating Procedures.

Requirements & Qualifications:

Employer requires a master’s degree in statistics, biostatistics, or a closely related scientific field and six (6) years of work experience as a statistician, or a closely related occupation, in the pharmaceutical or biotechnology industry. In addition, the employer requires the following:

1. Demonstrated knowledge of methodologies applied in clinical trials, with a focus on registration and life-cycle management, gained through at least six (6) years of work experience.
2. Demonstrated ability using SAS or R gained through at least six (6) years of work experience.
3. Demonstrated knowledge of CDISC SDTM/ADaM models gained through at least six (6) years of work experience.
4. Demonstrated knowledge of CRO and vendor oversight gained through at least six (6) years of work experience.
5. Demonstrated ability communicating statistical information to non-scientists in order to educate on complex statistical concepts gained through at least six (6) years of work experience.

All years of experience may be gained concurrently.

Salary range: $154,000 to $230,000 per year.

Applicants can submit their resumes to Relay Theraupeutics, Inc. (Attn: A. Manners), 60 Hampshire St., Cambridge, MA 02139, at recruitingteam@relaytx.com, or apply online here.

About Relay Therapeutics

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.

Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!