Clinical Data Manager
Jacksonville, FL · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
51 Katalyst Clinical Data Manager Jobs Hiring Near You
Clinical Data Manager
Jacksonville, FL · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Clinical Data Manager
Princeton, NJ · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Clinical Data Manager
Princeton, NJ · On-site
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. * Develop and manage data management timelines for multiple projects ...
Clinical Data manager
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Clinical Data manager
San Francisco, CA · On-site
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Clinical Data Manager
Austin, TX · On-site
The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock * The CDM ensures that data is accurate ...
Clinical Data Manager
Austin, TX · On-site
The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock * The CDM ensures that data is accurate ...
Provide support and oversight for the CRO Data Management team. * Collaborate with the team on study design, protocol development, CRF design, statistical planning, and CSRs. * Review clinical study ...
Provide support and oversight for the CRO Data Management team. * Collaborate with the team on study design, protocol development, CRF design, statistical planning, and CSRs. * Review clinical study ...
Clinical Data Manager
Boulder, CO · On-site
Develop and manage standard operation procedures (SOP and CLPs) for clinical investigation data management; Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC ...
Clinical Data Manager
Boulder, CO · On-site
Develop and manage standard operation procedures (SOP and CLPs) for clinical investigation data management; Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Cambridge, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Cambridge, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Irvine, CA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Irvine, CA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Boston, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Boston, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Durham, NC · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Durham, NC · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Boston, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead Clinical Data Manager
Boston, MA · On-site
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Clinical Data Manager
Charlotte, NC · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical Data Manager
Charlotte, NC · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical Data Manager
Dallas, TX · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical Data Manager
Dallas, TX · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical data manager
Omaha, NE · On-site
We are seeking a highly motivated and detail-oriented Clinical Data Manager to join our dynamic clinical research team. In this pivotal role, you will oversee the collection, management, and ...
Clinical data manager
Omaha, NE · On-site
We are seeking a highly motivated and detail-oriented Clinical Data Manager to join our dynamic clinical research team. In this pivotal role, you will oversee the collection, management, and ...
Clinical Data Manager
Chicago, IL · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical Data Manager
Chicago, IL · On-site
Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented; performs quality and accurate ...
Clinical Data Manager
Mountain View, CA · On-site
Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign off on the data transfer specifications, and transfer data from ...
Clinical Data Manager
Mountain View, CA · On-site
Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign off on the data transfer specifications, and transfer data from ...
The Senior Clinical Data Manager provides oversight and accountability and/or executes data management activities and/or performs scientific data review for multiple low, moderate and high complexity ...
The Senior Clinical Data Manager provides oversight and accountability and/or executes data management activities and/or performs scientific data review for multiple low, moderate and high complexity ...
Katalyst Jobs Information
What is it like to work at Katalyst?
Katalyst appears to be a collaborative and innovative company that values creativity and teamwork, fostering an environment where employees can share ideas and work together to achieve common goals.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
What makes Katalyst an attractive place to work?
Katalyst is a forward-thinking company that has established itself as a leader in its industry, known for its commitment to innovation and customer satisfaction. The company's work environment is characterized by a collaborative and dynamic atmosphere, where employees are encouraged to share ideas and work together to drive progress. Joining Katalyst offers opportunities for professional growth and development, as well as the chance to contribute to meaningful projects that can have a lasting impact.
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Job description
Responsibilities:
- Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting.
- Develop and manage data management timelines for multiple projects, ensuring all milestones are met according to project plans.
- Design, build, and oversee the implementation and management of clinical trial databases using Electronic Data Capture (EDC) systems (e.g., Medidata, Medrio, or similar).
- Develop and oversee maintenance all data management documentation for all clinical studies.
- Ensure clinical data is captured accurately and efficiently, incorporating appropriate data validation checks and edit checks.
- Oversee data validation processes, including data cleaning, discrepancy management, and query resolution.
- Ensure data accuracy, completeness, and compliance with regulatory requirements (e.g., FDA, EMA) and industry standards (CDISC, SDTM, WHO Drug, MedDRA).
- Perform data review and provide feedback to study teams to improve data quality and resolve issues early in the trial process.
- Ensure clinical data management activities are compliant with regulatory requirements (FDA, EMA), ICH GCP guidelines, and other relevant regulations.
- Prepare and contribute to regulatory submissions, including clinical study reports, and support data auditing processes.
- Collaborate with clinical operations, biostatistics, statistical programming, medical writing, scientific and regulatory teams to provide data management expertise in clinical trial planning and execution.
- Serve as the primary point of contact for data management vendors and external partners, ensuring effective communication and timely issue resolution.
- Manage independent vendor and CRO biostatistical services performance and oversee compliance with contracts while ensuring budgetary efficiency
- Develop, implement, and continuously improve clinical data management processes and systems.
- Lead initiatives to enhance the efficiency and effectiveness of clinical data management, including the evaluation of new tools, software, and methodologies.
- Bachelor's or master's degree in life sciences, health informatics, computer science, or related field. Advanced degree preferred.
- Strong understanding of data structure and data systems.
- Minimum of 5+ years of experience in clinical data management
- Proven experience managing data across multiple phases of clinical trials
- Proficiency with EDC systems (e.g., Medidata Rave, Medrio).
- Strong understanding of CDISC standards (CDASH, SDTM, ADaM) as well as WHO Drug and MedDRA coding.
- Familiarity with data reporting tools is a plus.
- Thorough understanding of clinical trial processes, regulatory requirements (e.g., FDA, EMA), and GCP standards.
- Strong leadership and project management skills, with the ability to manage multiple priorities in a fast-paced environment.
- Excellent communication, problem-solving, and decision-making skills.
- Ability to work collaboratively with cross-functional teams and manage
- relationships with external vendors.
- Certified Clinical Data Manager (CCDM) or similar certification is preferred.