Sr. Clinical Trial Manager/Associate Director
This a Full Remote job, the offer is available from: United States
Associate Director, Clinical Operations
Company Overview
QED Therapeutics, an affiliate within BridgeBio Pharma, focuses on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplasia. Achondroplasia is the most common form of genetically-driven short stature, which causes potentially debilitating medical complications. With our experimental therapeutic candidate, infigratinib, we seek to provide an option to children living with Achondroplasia and their families.
What You’ll Do
As Sr. CTM/Associate Director of Clinical Operations, you will be the cross-functional study team lead to oversee the planning, execution, and delivery of clinical trial operations, potentially across multiple studies. You will provide strong matrix management and guidance to ensure teams achieve key milestones on time and with quality. You will manage study operations within budget and established timelines, ensuring compliance with GCP, SOPs, and regulatory standards. In this role, you will champion collaboration and accountability across all aspects of study delivery.
Responsibilities
• Lead trial execution strategy and operational oversight by developing and driving the study operational plan, execution approach, and vendor-governance cadence, ensuring consistent progress toward major milestones and data deliverables.
• Lead study planning and management by coordinating the development, review, and maintenance of key study documents (e.g., investigator brochures, protocols, ICFs, CRFs, CSRs, training manuals) and monitor study progress and timelines in partnership with the study and clinical leads.
• Oversee quality control by developing, implementing, and training on SOPs, as well as creating monitoring and oversight processes to ensure compliance with GCP and regulatory guidelines.
• Responsible for developing and managing clinical trial budgets, including site agreements, forecasting, accruals, and FTE allocations; reviewing vendor invoices and reconciling site payments to ensure accuracy and identify variances.
• Build and maintain strong relationships with investigators and site staff, ensuring clear communication on study conduct, specimen tracking, and data review; organize investigator meetings as needed.
• Provide oversight of CROs and vendors, including selection, contracting, onboarding, and performance management; conduct gap analyses, manage risks, and resolve issues proactively.
• Partner with cross-functional teams to ensure efficient trial operations, including supply chain planning and coordination for clinical and non-clinical trial materials.
• Directly manage and develop team members (as applicable) by hiring/onboarding, setting clear goals, coaching, providing timely feedback, and ensuring resourcing and prioritization to deliver trial milestones with quality.
• undefined
Where You’ll Work
This is a U.S.-based remote role that will require quarterly or as-needed visits to our San Francisco Office.
Who You Are
• Hold a bachelor’s degree in a scientific/medical field (or equivalent experience).
• At least 10-12 years of Clinical Operations experience within the biopharma industry.
• Proven success leading cross-functional teams to deliver clinical trials from start-up through close-out, including financial oversight, data review, database lock, and reporting.
• Strong vendor management expertise and experience with submission-ready eTMF, quality assurance, SOP development, and CAPA management.
• In-depth knowledge of clinical trial design, protocol development, GCP, ICH E6 (R3), and GDPR, with preferred experience in rare/orphan disease studies.
• Recognized for leadership, with excellent communication, organizational, and multitasking skills; proficient in tools such as Smartsheet is a plus.
• Travel is required on a periodic basis to carry out responsibilities.
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
Salary
$177,700—$191,000 USD
This offer from "BridgeBio" has been enriched by Jobgether.com and got a 72% flex score.
Apply Now
Apply Now
Associate Director, Clinical Operations
Company Overview
QED Therapeutics, an affiliate within BridgeBio Pharma, focuses on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplasia. Achondroplasia is the most common form of genetically-driven short stature, which causes potentially debilitating medical complications. With our experimental therapeutic candidate, infigratinib, we seek to provide an option to children living with Achondroplasia and their families.
What You’ll Do
As Sr. CTM/Associate Director of Clinical Operations, you will be the cross-functional study team lead to oversee the planning, execution, and delivery of clinical trial operations, potentially across multiple studies. You will provide strong matrix management and guidance to ensure teams achieve key milestones on time and with quality. You will manage study operations within budget and established timelines, ensuring compliance with GCP, SOPs, and regulatory standards. In this role, you will champion collaboration and accountability across all aspects of study delivery.
Responsibilities
• Lead trial execution strategy and operational oversight by developing and driving the study operational plan, execution approach, and vendor-governance cadence, ensuring consistent progress toward major milestones and data deliverables.
• Lead study planning and management by coordinating the development, review, and maintenance of key study documents (e.g., investigator brochures, protocols, ICFs, CRFs, CSRs, training manuals) and monitor study progress and timelines in partnership with the study and clinical leads.
• Oversee quality control by developing, implementing, and training on SOPs, as well as creating monitoring and oversight processes to ensure compliance with GCP and regulatory guidelines.
• Responsible for developing and managing clinical trial budgets, including site agreements, forecasting, accruals, and FTE allocations; reviewing vendor invoices and reconciling site payments to ensure accuracy and identify variances.
• Build and maintain strong relationships with investigators and site staff, ensuring clear communication on study conduct, specimen tracking, and data review; organize investigator meetings as needed.
• Provide oversight of CROs and vendors, including selection, contracting, onboarding, and performance management; conduct gap analyses, manage risks, and resolve issues proactively.
• Partner with cross-functional teams to ensure efficient trial operations, including supply chain planning and coordination for clinical and non-clinical trial materials.
• Directly manage and develop team members (as applicable) by hiring/onboarding, setting clear goals, coaching, providing timely feedback, and ensuring resourcing and prioritization to deliver trial milestones with quality.
• undefined
Where You’ll Work
This is a U.S.-based remote role that will require quarterly or as-needed visits to our San Francisco Office.
Who You Are
• Hold a bachelor’s degree in a scientific/medical field (or equivalent experience).
• At least 10-12 years of Clinical Operations experience within the biopharma industry.
• Proven success leading cross-functional teams to deliver clinical trials from start-up through close-out, including financial oversight, data review, database lock, and reporting.
• Strong vendor management expertise and experience with submission-ready eTMF, quality assurance, SOP development, and CAPA management.
• In-depth knowledge of clinical trial design, protocol development, GCP, ICH E6 (R3), and GDPR, with preferred experience in rare/orphan disease studies.
• Recognized for leadership, with excellent communication, organizational, and multitasking skills; proficient in tools such as Smartsheet is a plus.
• Travel is required on a periodic basis to carry out responsibilities.
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
Salary
$177,700—$191,000 USD
This offer from "BridgeBio" has been enriched by Jobgether.com and got a 72% flex score.
Apply Now
Apply Now