Director, Clinical Data Management
To see similar active jobs please follow this link: Remote Development jobs
Our mission is to develop therapies that empower the immune system to combat neurodegeneration and our team is focused on developing treatments for some of the most challenging diseases facing our society. We are supported in this mission by experienced and accomplished scientists and clinicians, a novel portfolio of programs, leading healthcare investors, and pharma company partners, who share in our commitment to bettering the lives of patients and realizing a world where we make brain disorders history
As the Director of Clinical Data Management, will manage, lead, and be responsible for Clinical Data Management (CDM) planning and operational activities to meet corporate objectives and timelines within budgets. The Director of CDM will be responsible for supporting visions for the department including input into strategies, operations, infrastructure, technology, innovation, and talent development. The Director of CDM will require leadership and organization skills, and experience with early- to late-stage clinical trials. The Director will also collaborate closely with other functional areas and key partners to ensure quality results to meet business needs.
This position will report to the Senior Director of CDM and will enable data management capabilities to support the company's research and development efforts with the goal of creating exciting change in the way the world treats neurodegenerative disorders.
In your first year your goals will include but not limited to:
Promote standardization, automation, innovation, process improvement, and technology enhancement in CDM and beyond to increase drug development efficiency.
Support establishment of sound CDM processes including SOPs to ensure the highest data quality/integrity and regulatory compliance with FDA regulations, GCP, ICH guidelines and Good Clinical DM Practices.
Provide program oversight for CDM activities including CRF/eCRF design, validation programming, discrepancy management, and database development and production.
Ensure studies are executed on time, within budget, and in adherence to quality standards.
Champion and lead the development and implementation of policies, standards, and process improvement initiatives.
Ensure CROs, suppliers, and internal staff meet the highest quality standards per SOPs.
Provide oversight and guidance, as well as establishing key performance metrics with CROs to ensure the highest data quality/integrity and regulatory compliance.
Responsible for vendor and technology (e.g., EDC or IRT) evaluation, qualification, and selection.
Use scientific and drug development knowledge to anticipate and mitigate data management-related challenges during clinical trial execution.
Support strategic decision-making processes involving data management issues for ongoing clinical trials.
Promote productive collaboration between Biometrics & Digital Science and other functions (e.g., Biomarker, Clinical Operations, Clinical Science, Regulatory Affairs, QA, and IT) and ensure proper alignment around data management results.
Identify and implement solutions to global data management and EDC issues and concerns.
Provide strong leadership and inspiration to CDM staff. Recruit, develop, and motivate robust talents.
Work with the head of CDM for resource planning and budget forecasting. Provide input into budget, timelines, and resource needs for CDM with sound judgment and efficiency.
We'd love to hear from you if you possess the following:
Bachelor's or Masters degree in a scientific subject area.
Minimum 12 years of CDM experience in a pharmaceutical/biotech or CRO setting with at least 8 years of line management experience; global/international experience a must.
Sophisticated knowledge of CDM processes, EDC systems, database programming, quality management and technology advancements in the field of data management.
In-depth knowledge of FDA regulations, GCP, GCDMP, CDASH/CDISC, and ICH guidelines
Extensive experience in designing, leading and championing cross-functional projects with internal partners and CROs.
Understand Inspection Readiness and Regulatory considerations.
Consistent track record of line management and supervisory experience of CDM staff, proven leadership skills to lead and inspire CDM staff including consultants.
Outstanding problem-solving abilities and influencing/negotiation skills.
Excellent interpersonal, communication, and leadership skills.
Logical thinking, attention to detail and accuracy, good organizational skills, and problem-solving abilities.
Ability to prioritize and to adapt quickly to changing business conditions with a positive attitude.
Willing to travel if required.
Ability to prioritize workload and meet deadlines, demonstrate effective use of time and handle multiple priorities simultaneously.
Capable of actively identifying project challenges and risks and proposing appropriate solutions to issues.
$227,000 - $245,500 a year
Base salary ranges will be determined by the candidate’s level, qualifications, skill set, and experience
#LI-CH1
#LI-Remote
At Alector, our vision is bold, people are our priority, and our values are at the core of everything we do. Our dynamic and flexible environment encourages our teams to experiment, take ownership of decisions, and question convention to solve complex problems. We value shared wins, perseverance, and a growth mindset, which drives us forward, together.
Among the things you'll discover at Alector from your very first day are our committed and driven colleagues, a bold company vision, and new, modern offices designed to inspire innovation and collaboration in South San Francisco, right at the heart of Biotech Bay. Our benefits are thoughtfully designed around Alectorians and their loved ones and include flexible hybrid work options, competitive compensation, and comprehensive and unique benefits that enhance your health and well-being. Come join us!
We believe that hard-working teams include people from a wide variety of backgrounds and experiences who can challenge each other’s assumptions with fresh perspectives and bring creative ideas to the table. We are committed to building an open, diverse, and inclusive environment for all employees. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, sexual orientation, age, marital status, veteran status, or disability status, or any other characteristics protected under applicable federal, state, or local laws.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.
Review our Privacy Policy
About the job
Director, Clinical Data Management
To see similar active jobs please follow this link: Remote Development jobs
Our mission is to develop therapies that empower the immune system to combat neurodegeneration and our team is focused on developing treatments for some of the most challenging diseases facing our society. We are supported in this mission by experienced and accomplished scientists and clinicians, a novel portfolio of programs, leading healthcare investors, and pharma company partners, who share in our commitment to bettering the lives of patients and realizing a world where we make brain disorders history
As the Director of Clinical Data Management, will manage, lead, and be responsible for Clinical Data Management (CDM) planning and operational activities to meet corporate objectives and timelines within budgets. The Director of CDM will be responsible for supporting visions for the department including input into strategies, operations, infrastructure, technology, innovation, and talent development. The Director of CDM will require leadership and organization skills, and experience with early- to late-stage clinical trials. The Director will also collaborate closely with other functional areas and key partners to ensure quality results to meet business needs.
This position will report to the Senior Director of CDM and will enable data management capabilities to support the company's research and development efforts with the goal of creating exciting change in the way the world treats neurodegenerative disorders.
In your first year your goals will include but not limited to:
Promote standardization, automation, innovation, process improvement, and technology enhancement in CDM and beyond to increase drug development efficiency.
Support establishment of sound CDM processes including SOPs to ensure the highest data quality/integrity and regulatory compliance with FDA regulations, GCP, ICH guidelines and Good Clinical DM Practices.
Provide program oversight for CDM activities including CRF/eCRF design, validation programming, discrepancy management, and database development and production.
Ensure studies are executed on time, within budget, and in adherence to quality standards.
Champion and lead the development and implementation of policies, standards, and process improvement initiatives.
Ensure CROs, suppliers, and internal staff meet the highest quality standards per SOPs.
Provide oversight and guidance, as well as establishing key performance metrics with CROs to ensure the highest data quality/integrity and regulatory compliance.
Responsible for vendor and technology (e.g., EDC or IRT) evaluation, qualification, and selection.
Use scientific and drug development knowledge to anticipate and mitigate data management-related challenges during clinical trial execution.
Support strategic decision-making processes involving data management issues for ongoing clinical trials.
Promote productive collaboration between Biometrics & Digital Science and other functions (e.g., Biomarker, Clinical Operations, Clinical Science, Regulatory Affairs, QA, and IT) and ensure proper alignment around data management results.
Identify and implement solutions to global data management and EDC issues and concerns.
Provide strong leadership and inspiration to CDM staff. Recruit, develop, and motivate robust talents.
Work with the head of CDM for resource planning and budget forecasting. Provide input into budget, timelines, and resource needs for CDM with sound judgment and efficiency.
We'd love to hear from you if you possess the following:
Bachelor's or Masters degree in a scientific subject area.
Minimum 12 years of CDM experience in a pharmaceutical/biotech or CRO setting with at least 8 years of line management experience; global/international experience a must.
Sophisticated knowledge of CDM processes, EDC systems, database programming, quality management and technology advancements in the field of data management.
In-depth knowledge of FDA regulations, GCP, GCDMP, CDASH/CDISC, and ICH guidelines
Extensive experience in designing, leading and championing cross-functional projects with internal partners and CROs.
Understand Inspection Readiness and Regulatory considerations.
Consistent track record of line management and supervisory experience of CDM staff, proven leadership skills to lead and inspire CDM staff including consultants.
Outstanding problem-solving abilities and influencing/negotiation skills.
Excellent interpersonal, communication, and leadership skills.
Logical thinking, attention to detail and accuracy, good organizational skills, and problem-solving abilities.
Ability to prioritize and to adapt quickly to changing business conditions with a positive attitude.
Willing to travel if required.
Ability to prioritize workload and meet deadlines, demonstrate effective use of time and handle multiple priorities simultaneously.
Capable of actively identifying project challenges and risks and proposing appropriate solutions to issues.
$227,000 - $245,500 a year
Base salary ranges will be determined by the candidate’s level, qualifications, skill set, and experience
#LI-CH1
#LI-Remote
At Alector, our vision is bold, people are our priority, and our values are at the core of everything we do. Our dynamic and flexible environment encourages our teams to experiment, take ownership of decisions, and question convention to solve complex problems. We value shared wins, perseverance, and a growth mindset, which drives us forward, together.
Among the things you'll discover at Alector from your very first day are our committed and driven colleagues, a bold company vision, and new, modern offices designed to inspire innovation and collaboration in South San Francisco, right at the heart of Biotech Bay. Our benefits are thoughtfully designed around Alectorians and their loved ones and include flexible hybrid work options, competitive compensation, and comprehensive and unique benefits that enhance your health and well-being. Come join us!
We believe that hard-working teams include people from a wide variety of backgrounds and experiences who can challenge each other’s assumptions with fresh perspectives and bring creative ideas to the table. We are committed to building an open, diverse, and inclusive environment for all employees. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, sexual orientation, age, marital status, veteran status, or disability status, or any other characteristics protected under applicable federal, state, or local laws.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.
Review our Privacy Policy