Katalyst CRO
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Principal Clinical Data Manager
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Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Job Description
The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with regulatory standards. The Principal Clinical Data Manager serves as the lead contact for data management, collaborating cross-functionally with key stakeholders to drive efficient processes, maintain data integrity, and uphold industry best practices. Additionally, they act as the data steward, ensuring proper governance, documentation, and inspection readiness for all clinical data. Job Description
The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with regulatory standards. The Principal Clinical Data Manager serves as the lead contact for data management, collaborating cross-functionally with key stakeholders to drive efficient processes, maintain data integrity, and uphold industry best practices. Additionally, they act as the data steward, ensuring proper governance, documentation, and inspection readiness for all clinical data.
Responsibilities
Lead data management activities, ensuring accuracy, consistency, and compliance with regulatory standards. Oversee database build activities, data collection, coding, cleaning, and database lock. Develop and execute data management plans, including risk management strategies. Work closely with internal and external stakeholders, including Biostatistics, Clinical Development, Quality Assurance, and Regulatory Affairs, to facilitate seamless data flow and compliance. Serve as the primary data management contact for assigned therapeutic areas, ensuring proper planning and issue resolution. Ensure timely and quality deliverables within project timelines and budget constraints. Develop and implement validation checks, conduct data reviews, and resolve data discrepancies to maintain high data standards. Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, FDA regulations, and CDISC standards. Supervise database development, validation, and transfer processes in accordance with SOPs and regulatory requirements. Provide subject matter expertise in clinical data management systems, electronic data capture (EDC) platforms, and data standards such as CDISC. Develop and manage electronic Case Report Forms (eCRFs), data transfer specifications, and validation reports. Establish and refine data management standard operating procedures (SOPs) and best practices. Mentor and train junior data managers, fostering a collaborative environment and continuous learning culture. Ensure direct reports have adequate training and skills to meet regulatory and company standards. Guide teams on clinical data management best practices and evolving industry requirements. Maintain GCP inspection readiness by ensuring proper documentation and compliance with regulatory requirements. Serve as the primary point of contact for data management activities during audits and inspections. Review and approve key project documents, including Data Management Manuals, CRF Completion Guidelines, and validation specifications.
Requirements:
Bachelor's degree in clinical, biological, or mathematical sciences, nursing, or a related field. Minimum of 6+ years of clinical data management experience in pharmaceutical development or CRO environment. Extensive experience with clinical trials, EDC databases, IRT systems, and diary applications for data collection. Strong knowledge of GCP, ICH, FDA, and CDISC regulatory requirements governing clinical studies. Proven ability to develop SOPs, risk management strategies, and data management plans. Demonstrated leadership, problem-solving, and project management skills. Excellent organizational, communication, and collaboration skills with a team-oriented approach. Self-motivated with a commitment to high-quality, on-time deliverables.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
Job function Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new Clinical Data Manager jobs in
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Principal Clinical Data Manager
role at
Katalyst CRO Continue with Google Continue with Google 3 months ago Be among the first 25 applicants Join to apply for the
Principal Clinical Data Manager
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Sign in to access AI-powered advices
Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Continue with Google Job Description
The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with regulatory standards. The Principal Clinical Data Manager serves as the lead contact for data management, collaborating cross-functionally with key stakeholders to drive efficient processes, maintain data integrity, and uphold industry best practices. Additionally, they act as the data steward, ensuring proper governance, documentation, and inspection readiness for all clinical data. Job Description
The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with regulatory standards. The Principal Clinical Data Manager serves as the lead contact for data management, collaborating cross-functionally with key stakeholders to drive efficient processes, maintain data integrity, and uphold industry best practices. Additionally, they act as the data steward, ensuring proper governance, documentation, and inspection readiness for all clinical data.
Responsibilities
Lead data management activities, ensuring accuracy, consistency, and compliance with regulatory standards. Oversee database build activities, data collection, coding, cleaning, and database lock. Develop and execute data management plans, including risk management strategies. Work closely with internal and external stakeholders, including Biostatistics, Clinical Development, Quality Assurance, and Regulatory Affairs, to facilitate seamless data flow and compliance. Serve as the primary data management contact for assigned therapeutic areas, ensuring proper planning and issue resolution. Ensure timely and quality deliverables within project timelines and budget constraints. Develop and implement validation checks, conduct data reviews, and resolve data discrepancies to maintain high data standards. Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, FDA regulations, and CDISC standards. Supervise database development, validation, and transfer processes in accordance with SOPs and regulatory requirements. Provide subject matter expertise in clinical data management systems, electronic data capture (EDC) platforms, and data standards such as CDISC. Develop and manage electronic Case Report Forms (eCRFs), data transfer specifications, and validation reports. Establish and refine data management standard operating procedures (SOPs) and best practices. Mentor and train junior data managers, fostering a collaborative environment and continuous learning culture. Ensure direct reports have adequate training and skills to meet regulatory and company standards. Guide teams on clinical data management best practices and evolving industry requirements. Maintain GCP inspection readiness by ensuring proper documentation and compliance with regulatory requirements. Serve as the primary point of contact for data management activities during audits and inspections. Review and approve key project documents, including Data Management Manuals, CRF Completion Guidelines, and validation specifications.
Requirements:
Bachelor's degree in clinical, biological, or mathematical sciences, nursing, or a related field. Minimum of 6+ years of clinical data management experience in pharmaceutical development or CRO environment. Extensive experience with clinical trials, EDC databases, IRT systems, and diary applications for data collection. Strong knowledge of GCP, ICH, FDA, and CDISC regulatory requirements governing clinical studies. Proven ability to develop SOPs, risk management strategies, and data management plans. Demonstrated leadership, problem-solving, and project management skills. Excellent organizational, communication, and collaboration skills with a team-oriented approach. Self-motivated with a commitment to high-quality, on-time deliverables.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
Job function Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new Clinical Data Manager jobs in
Austin, TX . Public Health Data Analyst and Scientific Writer
Austin, TX $5,098.66 - $6,701.75 1 month ago Supervisor, Clinical Laboratory- TiH 2nd Shift
CMC Medication Aide Student Trainee - Travis Unit
Clinical Laboratory Supervisor-Horizon 2nd Shift
Senior Manager, Program Manager/Product Owner
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr