J&J Family of Companies
Senior Clinical Data Manager
J&J Family of Companies, Boston, Massachusetts, us, 02298
J&J Family of Companies Senior Clinical Data Manager Boston, Massachusetts Apply Now
Senior Clinical Data Manager - 2406217367WDescriptionJohnson and Johnson is currently seeking a
Senior Clinical Data Manager
located in Titusville, NJ; Raritan, NJ; OR Spring House, PA. Remote work options in the United States may be considered on a case-by-case basis and if approved by the company.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 trials. The Senior Clinical Data Manager makes recommendations and decisions that have an impact on processes, timing, and structure for trials and assignments with minimal direction from manager or Data Management Leader (DML). This position also makes recommendations for processes, timing, structure, and resources at a program level. Work is received in broad terms, reviewed during major deliverables, and the amount of instruction is limited. Work is reviewed with the Data Management Leaders, or the immediate manager as needed.Primary responsibilities:Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:o Gather and/or review content and integration requirements for eCRF and other data collection toolso Establish conventions and quality expectations for clinical datao Establish expectations for dataset content and structureo Set timelines and follow-up regularly to monitor delivery of all data management milestonesEnsure accurate review of related clinical data management documents as well as compliance with regulatory guidelines and documentation requirements.Ensure real-time inspection readiness of all DM deliverables for the trial; participate in Regulatory Agency and J&J internal audits as necessary.Lead the planning and tracking of content, format, quality, and timing of applicable data management deliverables. Ensure deliverables are on time.Take a leadership role to obtain and share best practices with internal partners. Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.Identify and participate in process, system, and tool improvement initiatives.Lead others in implementing process, system, and tool improvement initiatives.Perform (complex) scientific study data review and management of CDM, Study Responsible Scientist (SRS, and Study Responsible Physician related queries in EDC system. Involvement in other clinical data review activities (e.g., Coding, SAE reconciliation) is possible.Take a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.QualificationsEducation:Master’s degree or PhD preferredRequired:4 years experience in Pharmaceutical, CRO, Biotech, or Health related field or industryExperience in clinical drug development within the pharmaceutical or related industryExperience in clinical data review and knowledge of medical terminologyExperience working with cross functional stakeholders and teamsStrong written and verbal communication skillsTeam leadership experience (direct line management not required)Strong clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocolsIn-depth knowledge of current clinical drug development processesKnowledge of applicable international guidelines regarding data management of clinical trialsKnowledge or technology platforms and systems to capture and process data as well as understanding of data privacy rules in relation to clinical data exchangeKnowledge of current industry standard (i.e., CDISC, SDTM, CDASH, etc.)In-depth knowledge of project management and techniques10% travel (domestic & international)The anticipated base pay range for this position in the US is $105,000 to $169,050.The anticipated base pay range for this position in San Francisco Bay Area is $121,000 to $194,350.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Primary Location
NA-US-New Jersey-RaritanOther Locations
NA-United States, NA-US-Pennsylvania-Spring House, NA-US-New Jersey-Titusville
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Senior Clinical Data Manager - 2406217367WDescriptionJohnson and Johnson is currently seeking a
Senior Clinical Data Manager
located in Titusville, NJ; Raritan, NJ; OR Spring House, PA. Remote work options in the United States may be considered on a case-by-case basis and if approved by the company.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 trials. The Senior Clinical Data Manager makes recommendations and decisions that have an impact on processes, timing, and structure for trials and assignments with minimal direction from manager or Data Management Leader (DML). This position also makes recommendations for processes, timing, structure, and resources at a program level. Work is received in broad terms, reviewed during major deliverables, and the amount of instruction is limited. Work is reviewed with the Data Management Leaders, or the immediate manager as needed.Primary responsibilities:Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:o Gather and/or review content and integration requirements for eCRF and other data collection toolso Establish conventions and quality expectations for clinical datao Establish expectations for dataset content and structureo Set timelines and follow-up regularly to monitor delivery of all data management milestonesEnsure accurate review of related clinical data management documents as well as compliance with regulatory guidelines and documentation requirements.Ensure real-time inspection readiness of all DM deliverables for the trial; participate in Regulatory Agency and J&J internal audits as necessary.Lead the planning and tracking of content, format, quality, and timing of applicable data management deliverables. Ensure deliverables are on time.Take a leadership role to obtain and share best practices with internal partners. Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.Identify and participate in process, system, and tool improvement initiatives.Lead others in implementing process, system, and tool improvement initiatives.Perform (complex) scientific study data review and management of CDM, Study Responsible Scientist (SRS, and Study Responsible Physician related queries in EDC system. Involvement in other clinical data review activities (e.g., Coding, SAE reconciliation) is possible.Take a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.QualificationsEducation:Master’s degree or PhD preferredRequired:4 years experience in Pharmaceutical, CRO, Biotech, or Health related field or industryExperience in clinical drug development within the pharmaceutical or related industryExperience in clinical data review and knowledge of medical terminologyExperience working with cross functional stakeholders and teamsStrong written and verbal communication skillsTeam leadership experience (direct line management not required)Strong clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocolsIn-depth knowledge of current clinical drug development processesKnowledge of applicable international guidelines regarding data management of clinical trialsKnowledge or technology platforms and systems to capture and process data as well as understanding of data privacy rules in relation to clinical data exchangeKnowledge of current industry standard (i.e., CDISC, SDTM, CDASH, etc.)In-depth knowledge of project management and techniques10% travel (domestic & international)The anticipated base pay range for this position in the US is $105,000 to $169,050.The anticipated base pay range for this position in San Francisco Bay Area is $121,000 to $194,350.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Primary Location
NA-US-New Jersey-RaritanOther Locations
NA-United States, NA-US-Pennsylvania-Spring House, NA-US-New Jersey-Titusville
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