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Head of Clinical Research
2 months ago
Our Culture:
Why consider a career with us?
At Foghorn Therapeutics, we embrace the philosophy of "People First, Mission Always."
We prioritize our people because they are the cornerstone of our achievements.
We celebrate the diversity of backgrounds, ideas, perspectives, and experiences that our team members contribute to Foghorn Therapeutics – as evidenced by our community speaking over 22 languages and representing more than 24 nationalities.
We regard our colleagues as individuals, not merely as employees – a principle reflected in our actions that demonstrate our care for them, their families, and their lives.
We emphasize "Mission Always" because we recognize that a steadfast commitment to our mission can profoundly impact the lives of others.
We are dedicated to developing a novel class of therapies aimed at enhancing the lives of over 2.5 million individuals affected by cancer.
Our culture is rooted in achieving success through data evaluation, fostering an environment where relationships can thrive and grow.Our Science:
The innovative science behind our therapies continues to provide essential insights into diseases that have perplexed healthcare professionals and researchers.
Our fundamental scientific approach focuses on the chromatin regulatory system, which precisely regulates the activation and suppression of specific DNA segments.
Disruptions in the chromatin regulatory system can lead to a variety of diseases, including cancer, affecting millions globally.Our proprietary Gene Traffic Control platform serves as a powerful mechanism for understanding and modulating the chromatin regulatory system. We are actively pursuing multiple treatment options for these disruptions.
We are uniquely positioned as the only organization capable of studying and targeting the chromatin regulatory system comprehensively, contextually, and integratively.
The Role:
As the Head of Clinical Research at Foghorn, a pioneer in the development of groundbreaking oncology therapies, you will steer the progression of clinical programs that can transform patient outcomes.
By leading the strategic design, execution, and evaluation of clinical trials, you will uphold the highest standards of scientific integrity and ethical research practices.
Your expertise will influence critical decision-making processes, ultimately facilitating the introduction of innovative and life-altering therapies to those in need.This position requires a hybrid work model, necessitating regular office attendance.
In This Role, You'll Get To:
Lead Strategic Clinical Development:
Provide expert direction on Phase I/II/III programs, formulating protocols and clinical development strategies that advance scientific goals while strictly adhering to regulatory standards.
Analyze and Interpret Clinical Data:
Diligently supervise the collection and analysis of clinical data, employing advanced tools to ensure data integrity and deliver actionable insights that inform program decisions.
Enhance Trial Processes:
Collaborate with data management teams to optimize clinical databases and data collection methods, maximizing efficiency and accuracy.
Ensure Regulatory Compliance:
Protect trial integrity by closely monitoring adherence to all ethical and regulatory guidelines, promptly addressing any potential issues.
Assist with Regulatory Submissions:
Aid in the preparation of scientifically sound and compliant documentation for regulatory interactions.
Share Clinical Knowledge:
Support the development of presentations, publications, and conference materials that enhance understanding within the field.
Foster Cross-Functional Collaboration:
Build strong partnerships across 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 relevant clinical research experience is required.
Knowledge:
Comprehensive understanding of GCP and ICH guidelines.
Experience: 7+ years of demonstrated experience in clinical trial management and oversight, particularly in oncology. Proven success in leading Phase I-III clinical trials. History of analyzing and interpreting clinical data, including proficiency with data review software.
Skills:
Demonstrated analytical capabilities, including expertise in statistical analysis and data interpretation related to clinical trials.
Expertise in clinical study design, including protocol and amendment development.
Thorough knowledge of regulatory guidelines (e.g., FDA, EMA, ICH, GCP).
Proficiency in data management tools and processes, including oversight of database setups and modifications.
Strong leadership and team management skills, with a focus on mentoring staff and leading cross-functional teams.
Motivation to embrace new challenges and responsibilities.
Exceptional written and verbal communication skills, including scientific writing and regulatory presentations.
Benefits
Foghorn Therapeutics is pleased to offer you and your family 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 company matching
Corporate Wellness Program
Unlimited Paid Time Off policy
Winter shutdown
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.
Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work
Company lunches on Wednesdays
Foghorn Therapeutics maintains 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.
