AbbVieBoston, 4 mi from Cambridge
and validation of ADaM and TLFs for all safety deliverables following AbbVie’s SOPs, department, and project standards.
Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
Creates...
AbbVieBoston, 4 mi from Cambridge
Statistical Programmers, Statistical Analysts and Senior Statistical Analysts...
Costello MedicalBoston, 4 mi from Cambridge
Role Summary
Responsibilities: You will be responsible for devising and performing statistical analysis plans and then communicating the methodologies and results of these to our clients in the healthcare sector
Salary: $73,000 to $76,000...
MITREBedford
N162 is seeking a Data Scientist who wants to deliver innovative solutions to unique national challenges. Lead the execution of data analytics and machine learning projects, responsible for the full data analytics lifecycle. These technologies included applied physics, signal processing, electronic ...
SAICHanscom Air Force Base
Azure Cloud Software Developer and Engineer. Azure Cloud Software Developer and Engineer. Deploy software packages to the Cloud One Integration, Test and Production environments. Agile, Scrum, SAFe or other modern software development methods/practices.
...
MITREBedford
Work independently and on teams to develop software prototypes using modern software engineering techniques with minimal instruction, guidance, and direction. Strong fundamentals in software engineering, object-oriented programming, web application development, and software architecture.
MITRE’sColl...
ACL DigitalCambridge
status and risks associated with integrated timelines to leadership
• Ability to manage multiple, competing priorities simultaneously
• Statistical analysis, and knowledge of Gage R&R,
Ideal candidate: 3 YOE in field desired with bachelors. Experience...
Barrington James LimitedBoston, 4 mi from Cambridge
and analytical strategies, offering insights into protocols, and creating and reviewing statistical analysis plans.
Key Responsibilities:
1. Lead biostatistical efforts on real-world data studies, overseeing the creation of statistical analysis plans (SAPs...
Get new jobs by email!
Get email updates for the latest Statistical Analyst jobs in Cambridge
It's free, and you can cancel email updates at any time
Director, Clinical Science
Foghorn Therapeutics | Cambridge | Full-time | apply.workable.com |
Our Culture: Why work with us?
At Foghorn Therapeutics, we believe in “People First, Mission Always.”
We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities.
We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives.
We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of over 2.5 million people with cancer.
Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop.
Our Science:
The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time.
Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.
Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way.
The Role:
As the Director of Clinical Science at Foghorn, a leader in the development of innovative oncology treatments, you'll guide the advancement of clinical programs that transform the lives of patients. Leading the strategic design, implementation, and analysis of clinical trials, you'll uphold the highest standards of scientific rigor and ethical research.
Your insights will drive critical decision-making, ultimately bringing novel and life-changing therapies to those in need.
In This Role, You'll Get To:
• Champion Strategic Clinical Development: Provide expert guidance on Phase I/II/III programs, crafting protocols and clinical development plans that advance scientific objectives and rigorously adhere to regulatory standards.
• Analyze and Interpret Clinical Data: Diligently oversee the collection and analysis of clinical data, using sophisticated tools to ensure data integrity and offer actionable insights that drive program decisions.
• Optimize Trial Processes: Collaborate with data management to streamline clinical databases and data collection, maximizing efficiency and accuracy.
• Uphold Regulatory Compliance: Safeguard trial integrity by meticulously monitoring adherence to all ethical and regulatory guidelines, swiftly addressing potential issues.
• Contribute to Regulatory Submissions: Support the preparation of scientifically sound and compliant documents for regulatory interactions.
• Disseminate Clinical Knowledge: Support the creation of presentations, publications, and conference materials that advance understanding within the field.
• Nurture Cross-Functional Excellence: Build strong partnerships throughout the organization, bridging the gap between clinical science, pharmacology, medicine, and regulatory functions.
Requirements
About You:
• Education: A Master's Degree, Ph.D., PharmD, or a B.A./B.S. with commensurate clinical research experience is required.
• Knowledge: Robust understanding of GCP and ICH guidelines.
• Experience: 7+ years of proven experience in clinical trial management and oversight, specifically within oncology. Demonstrated success in leading Phase I-III clinical trials. Track record of analyzing and interpreting clinical data, including the use of data review software.
• Skills:
• Proven analytical prowess, including proficiency in statistical analysis and data interpretation related to clinical trials.
• Command of clinical study design, including protocol and amendment development.
• Comprehensive knowledge of regulatory guidelines (e.g., FDA, EMA, ICH, GCP).
• Fluency in data management tools and processes, including the ability to oversee database setups and modifications.
• Strong leadership and team management capabilities, with a focus on mentoring staff and leading cross-functional teams.
• Drive to embrace new challenges and responsibilities.
• Exceptional written and verbal communication, including scientific writing and regulatory presentations.
Benefits
Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:
• Highly competitive and inclusive medical, dental and vision coverage options
• BCBS PPO and PPO HSA plans
• BCBS Dental Plan
• EyeMed Vision Plan
• FSA and HSA for medical expenses and dependent care expenses
• 401(k) Program via Fidelity with the company match
• Corporate Wellness Program
• Unlimited Paid Time Off policy
• Winter shut down
• 12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.
• Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
• Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work
• Company lunches on Wednesdays
Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment.
Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
At Foghorn Therapeutics, we believe in “People First, Mission Always.”
We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities.
We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives.
We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of over 2.5 million people with cancer.
Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop.
Our Science:
The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time.
Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.
Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way.
The Role:
As the Director of Clinical Science at Foghorn, a leader in the development of innovative oncology treatments, you'll guide the advancement of clinical programs that transform the lives of patients. Leading the strategic design, implementation, and analysis of clinical trials, you'll uphold the highest standards of scientific rigor and ethical research.
Your insights will drive critical decision-making, ultimately bringing novel and life-changing therapies to those in need.
In This Role, You'll Get To:
• Champion Strategic Clinical Development: Provide expert guidance on Phase I/II/III programs, crafting protocols and clinical development plans that advance scientific objectives and rigorously adhere to regulatory standards.
• Analyze and Interpret Clinical Data: Diligently oversee the collection and analysis of clinical data, using sophisticated tools to ensure data integrity and offer actionable insights that drive program decisions.
• Optimize Trial Processes: Collaborate with data management to streamline clinical databases and data collection, maximizing efficiency and accuracy.
• Uphold Regulatory Compliance: Safeguard trial integrity by meticulously monitoring adherence to all ethical and regulatory guidelines, swiftly addressing potential issues.
• Contribute to Regulatory Submissions: Support the preparation of scientifically sound and compliant documents for regulatory interactions.
• Disseminate Clinical Knowledge: Support the creation of presentations, publications, and conference materials that advance understanding within the field.
• Nurture Cross-Functional Excellence: Build strong partnerships throughout the organization, bridging the gap between clinical science, pharmacology, medicine, and regulatory functions.
Requirements
About You:
• Education: A Master's Degree, Ph.D., PharmD, or a B.A./B.S. with commensurate clinical research experience is required.
• Knowledge: Robust understanding of GCP and ICH guidelines.
• Experience: 7+ years of proven experience in clinical trial management and oversight, specifically within oncology. Demonstrated success in leading Phase I-III clinical trials. Track record of analyzing and interpreting clinical data, including the use of data review software.
• Skills:
• Proven analytical prowess, including proficiency in statistical analysis and data interpretation related to clinical trials.
• Command of clinical study design, including protocol and amendment development.
• Comprehensive knowledge of regulatory guidelines (e.g., FDA, EMA, ICH, GCP).
• Fluency in data management tools and processes, including the ability to oversee database setups and modifications.
• Strong leadership and team management capabilities, with a focus on mentoring staff and leading cross-functional teams.
• Drive to embrace new challenges and responsibilities.
• Exceptional written and verbal communication, including scientific writing and regulatory presentations.
Benefits
Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:
• Highly competitive and inclusive medical, dental and vision coverage options
• BCBS PPO and PPO HSA plans
• BCBS Dental Plan
• EyeMed Vision Plan
• FSA and HSA for medical expenses and dependent care expenses
• 401(k) Program via Fidelity with the company match
• Corporate Wellness Program
• Unlimited Paid Time Off policy
• Winter shut down
• 12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.
• Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
• Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work
• Company lunches on Wednesdays
Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment.
Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Best jobs you don't want to miss: