Formation Bio
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Director, Clinical Project Management
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Formation Bio
About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, Sam Altman, John Doerr, Spark Capital, SV Angel Growth, and others.
Our Vision for AI in Pharma
Our Current Drug Portfolio
Our Technology & Platform
About The Position The Director of Clinical Project Management will provide overall leadership and strategic direction for the clinical project management functions in a technology-driven, AI-focused biotech environment. This individual will be responsible for leading multiple clinical programs across various therapeutic areas and phases (I–IV), ensuring compliance with global regulations, delivering on timelines and budgets, and driving a culture that leverages technology and AI platforms to enhance efficiency and scalability.
Responsibilities
Provide strategic and tactical guidance for ongoing and newly launched clinical studies, ensuring alignment with corporate and asset development goals, timelines, and budget parameters.
Maintain accountability for project deliverables, including overall timelines, budget forecasts, and resource allocation.
Ensure all clinical trials comply with ICH‑GCP, FDA regulations, and other applicable regulatory standards.
Champion proactive risk management by identifying and mitigating risks before they escalated.
Oversee vendor relationships and governance, holding external partners to high standards of quality, cost control, and on‑time deliverables.
Serve as the Operations Lead for clinical assets and associated studies, stepping in as the Clinical Project Manager when needs arise.
Develop and implement operational strategies for programs and clinical studies.
Collaborate with cross‑functional teams (Clinical Development, Regulatory, Program Management, etc.) to shape and refine Clinical Development Plans, ensuring feasibility and operational excellence.
Support protocol development and development of essential documents (e.g., Investigator’s Brochures, informed consent forms) by providing critical operational insights.
Remain current on emerging industry trends, regulatory updates, and best practices, pivoting operational strategies to maintain competitive advantage.
Leverage AI‑powered tools and technology platforms to streamline clinical processes.
Collaborate with internal and external tech partners to evaluate and implement cutting‑edge solutions.
About You
Bachelor’s degree in life sciences, nursing, pharmacy, or a related field.
Minimum of 10 years of clinical project management/clinical operations experience, including at least 5 years in a leadership capacity.
Proven track record in managing complex global trials across multiple phases (I–IV) and therapeutic areas.
Experience working within a sponsor company.
Experience in the integrated in‑house clinical trial execution model.
Experience working with CROs and managing complex, multi‑center clinical trials.
In‑depth knowledge of ICH‑GCP, FDA regulations, and global clinical trial guidelines.
Strong strategic thinking and analytical skills.
Strong project management skills, with the ability to manage multiple priorities and meet tight deadlines.
Excellent communication, interpersonal, and problem‑solving skills.
Preferred: Advanced degree (e.g., MSc, PhD, MBA) in a related field.
Location & Compensation Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with additional growth in the Research Triangle (NC) and San Francisco Bay Area. Please only apply if you reside in these locations or are willing to relocate. The target salary range for this role is $205,000–$250,000. Salary ranges are informed by a number of factors including geographic location. The range provided includes base salary only. In addition to base salary, we offer equity, comprehensive benefits, generous perks, hybrid flexibility, and more. If this range doesn't match your expectations, please still apply because we may have something else for you.
You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
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Director, Clinical Project Management
role at
Formation Bio
About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, Sam Altman, John Doerr, Spark Capital, SV Angel Growth, and others.
Our Vision for AI in Pharma
Our Current Drug Portfolio
Our Technology & Platform
About The Position The Director of Clinical Project Management will provide overall leadership and strategic direction for the clinical project management functions in a technology-driven, AI-focused biotech environment. This individual will be responsible for leading multiple clinical programs across various therapeutic areas and phases (I–IV), ensuring compliance with global regulations, delivering on timelines and budgets, and driving a culture that leverages technology and AI platforms to enhance efficiency and scalability.
Responsibilities
Provide strategic and tactical guidance for ongoing and newly launched clinical studies, ensuring alignment with corporate and asset development goals, timelines, and budget parameters.
Maintain accountability for project deliverables, including overall timelines, budget forecasts, and resource allocation.
Ensure all clinical trials comply with ICH‑GCP, FDA regulations, and other applicable regulatory standards.
Champion proactive risk management by identifying and mitigating risks before they escalated.
Oversee vendor relationships and governance, holding external partners to high standards of quality, cost control, and on‑time deliverables.
Serve as the Operations Lead for clinical assets and associated studies, stepping in as the Clinical Project Manager when needs arise.
Develop and implement operational strategies for programs and clinical studies.
Collaborate with cross‑functional teams (Clinical Development, Regulatory, Program Management, etc.) to shape and refine Clinical Development Plans, ensuring feasibility and operational excellence.
Support protocol development and development of essential documents (e.g., Investigator’s Brochures, informed consent forms) by providing critical operational insights.
Remain current on emerging industry trends, regulatory updates, and best practices, pivoting operational strategies to maintain competitive advantage.
Leverage AI‑powered tools and technology platforms to streamline clinical processes.
Collaborate with internal and external tech partners to evaluate and implement cutting‑edge solutions.
About You
Bachelor’s degree in life sciences, nursing, pharmacy, or a related field.
Minimum of 10 years of clinical project management/clinical operations experience, including at least 5 years in a leadership capacity.
Proven track record in managing complex global trials across multiple phases (I–IV) and therapeutic areas.
Experience working within a sponsor company.
Experience in the integrated in‑house clinical trial execution model.
Experience working with CROs and managing complex, multi‑center clinical trials.
In‑depth knowledge of ICH‑GCP, FDA regulations, and global clinical trial guidelines.
Strong strategic thinking and analytical skills.
Strong project management skills, with the ability to manage multiple priorities and meet tight deadlines.
Excellent communication, interpersonal, and problem‑solving skills.
Preferred: Advanced degree (e.g., MSc, PhD, MBA) in a related field.
Location & Compensation Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with additional growth in the Research Triangle (NC) and San Francisco Bay Area. Please only apply if you reside in these locations or are willing to relocate. The target salary range for this role is $205,000–$250,000. Salary ranges are informed by a number of factors including geographic location. The range provided includes base salary only. In addition to base salary, we offer equity, comprehensive benefits, generous perks, hybrid flexibility, and more. If this range doesn't match your expectations, please still apply because we may have something else for you.
You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
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