Formation Bio
Director, Clinical Trial Management
The Director of Clinical Trial Management is responsible for leading and overseeing the clinical monitoring aspects of clinical trials from study design through closeout. This role ensures that trials are executed efficiently, on time, and in compliance with all regulatory requirements. The Director will manage a team of Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) and will collaborate closely with cross-functional teams to achieve the strategic objectives of the clinical development programs. Leadership and Strategy: Develop and implement scalable clinical trial management strategies with a technology first, additional headcount second mentality. Provide leadership, direction, and oversight to the clinical trial management team. Facilitate effective communication and collaboration between internal teams and external partners. Maintain up-to-date knowledge of industry trends, regulatory requirements, and emerging best practices. Trial Management: Strategically build and implement in-house clinical trial capabilities. Develop the trial management team and processes to be flexible. Support the selection, contracting, and performance of Contract Research Organizations (CROs) and other external vendors. Ensure that all clinical trials are conducted in accordance with ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements. Ensure that clinical trials are conducted to the highest quality standards. Support internal and external audits and regulatory inspections. Team Development and Management: Recruit, mentor, and develop Clinical Trial Managers and CRAs. Conduct performance reviews, provide feedback, and support the professional growth of team members. Ensure that the clinical trial management team is trained on current SOPs, regulatory requirements, and industry best practices. About You: Bachelors degree in life sciences, nursing, pharmacy, or a related field (advanced degree preferred). Minimum of 10 years of experience in clinical trial management, with at least 5 years in a leadership role. Extensive experience managing clinical trials across multiple phases (I-IV) and therapeutic areas. Experience working within a sponsor company. Experience working with CROs and managing complex, multi-center clinical trials and/or experience working in an integrated in-house clinical trial execution model. In-depth knowledge of ICH-GCP, FDA regulations, and global clinical trial guidelines. Strong strategic thinking and analytical skills. Proven ability to lead and develop high-performing teams in a fast-paced, dynamic environment. Strong project management skills, with the ability to manage multiple priorities and meet tight deadlines. Excellent communication, interpersonal, and problem-solving skills. Ability to travel as required (up to 25%). Preferred: Advanced degree (e.g., MSc, PhD, MBA) in a related field. Preferred: Experience with global clinical trials and regulatory submissions. 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: $200,000 - $250,000. 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.
The Director of Clinical Trial Management is responsible for leading and overseeing the clinical monitoring aspects of clinical trials from study design through closeout. This role ensures that trials are executed efficiently, on time, and in compliance with all regulatory requirements. The Director will manage a team of Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) and will collaborate closely with cross-functional teams to achieve the strategic objectives of the clinical development programs. Leadership and Strategy: Develop and implement scalable clinical trial management strategies with a technology first, additional headcount second mentality. Provide leadership, direction, and oversight to the clinical trial management team. Facilitate effective communication and collaboration between internal teams and external partners. Maintain up-to-date knowledge of industry trends, regulatory requirements, and emerging best practices. Trial Management: Strategically build and implement in-house clinical trial capabilities. Develop the trial management team and processes to be flexible. Support the selection, contracting, and performance of Contract Research Organizations (CROs) and other external vendors. Ensure that all clinical trials are conducted in accordance with ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements. Ensure that clinical trials are conducted to the highest quality standards. Support internal and external audits and regulatory inspections. Team Development and Management: Recruit, mentor, and develop Clinical Trial Managers and CRAs. Conduct performance reviews, provide feedback, and support the professional growth of team members. Ensure that the clinical trial management team is trained on current SOPs, regulatory requirements, and industry best practices. About You: Bachelors degree in life sciences, nursing, pharmacy, or a related field (advanced degree preferred). Minimum of 10 years of experience in clinical trial management, with at least 5 years in a leadership role. Extensive experience managing clinical trials across multiple phases (I-IV) and therapeutic areas. Experience working within a sponsor company. Experience working with CROs and managing complex, multi-center clinical trials and/or experience working in an integrated in-house clinical trial execution model. In-depth knowledge of ICH-GCP, FDA regulations, and global clinical trial guidelines. Strong strategic thinking and analytical skills. Proven ability to lead and develop high-performing teams in a fast-paced, dynamic environment. Strong project management skills, with the ability to manage multiple priorities and meet tight deadlines. Excellent communication, interpersonal, and problem-solving skills. Ability to travel as required (up to 25%). Preferred: Advanced degree (e.g., MSc, PhD, MBA) in a related field. Preferred: Experience with global clinical trials and regulatory submissions. 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: $200,000 - $250,000. 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.