At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Beerse Antwerp Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for an Analyst II Clinical Data Manager in Beerse Belgium.
Purpose: The Analyst II Clinical Data Manager is a professional individual contributor role at junior level that provides oversight and accountability and/or executes data management activities and/or performs scientific data review for more than one trial of low to moderate complexity or for one high complexity trial. The Analyst II Data Manager makes recommendations and influences decisions for specific trials or assignments. This position analyzes and provides input into decisions with direction from manager or Data Management Leader (DML). Work is received in broad terms. Work is reviewed on an ongoing basis with Data Management Leader and the amount of instruction is limited.
You will be responsible for:
- 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:
- Gather and/or review content and integration requirements for eCRF and other data collection tools.
- Establish conventions and quality expectations for clinical data.
- Establish expectations for dataset content and structure.
- Set timelines and follow-up regularly to monitor delivery of all data management milestones.
- Review clinical data management documents (including submission package) ensuring appropriate quality scientific content organization clarity accuracy format and consistency. Ensure compliance with regulatory guidelines and the documentation matrix.
- Ensure real-time inspection readiness of all DM deliverables for the trial and participate in regulatory agency and J&J internal audits as necessary.
- Plan and track content format quality and timing of applicable data management deliverables. Ensure deliverables are on time.
- Take a leadership role with the assigned clinical working group(s) to ensure that DM and TA trial needs and deliverables are achieved.
- Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality scientific content organization clarity accuracy format and consistency.
- Identify and communicate lessons learned best practices and frequently asked questions at the trial level.
- Identify and participate in 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.
- Collaborate with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.
Principal Relationships:
- Reports into people manager position within functional area (e.g. Data Management Leader).
- Functional contacts within IDAR include but not limited to: Leaders and/or leads in Data Management and Central Monitoring Clinical and Statistical Programming Clinical Data Standards Regulatory Medical Writing IDAR Therapeutic Area Lead and system support organizations.
- Functional Contacts within J&J Innovative Medicine (as collaborator or peer) include but not limited to: Global Program Leaders Global Trial Leaders Biostatisticians Clinical Teams Procurement Finance Legal Global Privacy Regulatory Strategic Partnerships Human Resources and Project Coordinators.
- External contacts include but not limited to: External partners and suppliers CRO management and vendor liaisons industry peers and working groups.
Qualifications/Requirements:
- Minimum of a Bachelors degree (e.g. BS BA) or equivalent professional experience is required preferably in Clinical Data Management Health or Computer Sciences. Advanced degrees preferred (e.g. Master PhD).
- Minimum of 2 years of experience in Pharmaceutical CRO or Biotech industry or related field or industry.
- Experience in clinical drug development within the pharmaceutical industry or related industry.
- Experience working with cross functional stakeholders and teams.
- Strong written and verbal communications skills (in English).
Preferred
- Team leadership experience.
- Clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocols
- In-depth knowledge of current clinical drug development processes.
- In-depth knowledge of applicable international guidelines regarding data management of clinical trials.
- Knowledge of technology platforms and systems to capture and process data as well as understanding of data privacy rules in relation to clinical data exchange.
Other:
- Approx. <10% travel (domestic or international) may be required.
Required Skills:
Preferred Skills:
Advanced Analytics Biostatistics Business Behavior Clinical Data Management Clinical Operations Communication Cross-Functional Collaboration Database Applications Data Privacy Standards Data Savvy Good Clinical Practice (GCP) Organizing Problem Solving Report Writing Standard Operating Procedure (SOP) Systems Analysis
Required Experience:
Manager
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Beerse Antwerp Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for an Analyst II Clinical Data Manager in Beerse Belgium.
Purpose: The Analyst II Clinical Data Manager is a professional individual contributor role at junior level that provides oversight and accountability and/or executes data management activities and/or performs scientific data review for more than one trial of low to moderate complexity or for one high complexity trial. The Analyst II Data Manager makes recommendations and influences decisions for specific trials or assignments. This position analyzes and provides input into decisions with direction from manager or Data Management Leader (DML). Work is received in broad terms. Work is reviewed on an ongoing basis with Data Management Leader and the amount of instruction is limited.
You will be responsible for:
- 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:
- Gather and/or review content and integration requirements for eCRF and other data collection tools.
- Establish conventions and quality expectations for clinical data.
- Establish expectations for dataset content and structure.
- Set timelines and follow-up regularly to monitor delivery of all data management milestones.
- Review clinical data management documents (including submission package) ensuring appropriate quality scientific content organization clarity accuracy format and consistency. Ensure compliance with regulatory guidelines and the documentation matrix.
- Ensure real-time inspection readiness of all DM deliverables for the trial and participate in regulatory agency and J&J internal audits as necessary.
- Plan and track content format quality and timing of applicable data management deliverables. Ensure deliverables are on time.
- Take a leadership role with the assigned clinical working group(s) to ensure that DM and TA trial needs and deliverables are achieved.
- Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality scientific content organization clarity accuracy format and consistency.
- Identify and communicate lessons learned best practices and frequently asked questions at the trial level.
- Identify and participate in 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.
- Collaborate with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.
Principal Relationships:
- Reports into people manager position within functional area (e.g. Data Management Leader).
- Functional contacts within IDAR include but not limited to: Leaders and/or leads in Data Management and Central Monitoring Clinical and Statistical Programming Clinical Data Standards Regulatory Medical Writing IDAR Therapeutic Area Lead and system support organizations.
- Functional Contacts within J&J Innovative Medicine (as collaborator or peer) include but not limited to: Global Program Leaders Global Trial Leaders Biostatisticians Clinical Teams Procurement Finance Legal Global Privacy Regulatory Strategic Partnerships Human Resources and Project Coordinators.
- External contacts include but not limited to: External partners and suppliers CRO management and vendor liaisons industry peers and working groups.
Qualifications/Requirements:
- Minimum of a Bachelors degree (e.g. BS BA) or equivalent professional experience is required preferably in Clinical Data Management Health or Computer Sciences. Advanced degrees preferred (e.g. Master PhD).
- Minimum of 2 years of experience in Pharmaceutical CRO or Biotech industry or related field or industry.
- Experience in clinical drug development within the pharmaceutical industry or related industry.
- Experience working with cross functional stakeholders and teams.
- Strong written and verbal communications skills (in English).
Preferred
- Team leadership experience.
- Clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocols
- In-depth knowledge of current clinical drug development processes.
- In-depth knowledge of applicable international guidelines regarding data management of clinical trials.
- Knowledge of technology platforms and systems to capture and process data as well as understanding of data privacy rules in relation to clinical data exchange.
Other:
- Approx. <10% travel (domestic or international) may be required.
Required Skills:
Preferred Skills:
Advanced Analytics Biostatistics Business Behavior Clinical Data Management Clinical Operations Communication Cross-Functional Collaboration Database Applications Data Privacy Standards Data Savvy Good Clinical Practice (GCP) Organizing Problem Solving Report Writing Standard Operating Procedure (SOP) Systems Analysis
Required Experience:
Manager
View more
View less