Planet Pharma
Clinical Data Management Specialist
Planet Pharma, Libertyville, Illinois, United States, 60092
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Clinical Data Management Specialist
role at
Planet Pharma
Summary The Specialist, Clinical Data Management (CDM) is a leader in supporting clinical studies for medical device products and services. The CDM leads all aspects of clinical data management from study planning to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer. The CDM regularly collaborates with Global Clinical Affairs (GCA) study team members (Clinical Project Management, Biostatistics, Clinical Operations, Clinical Scientist) and cross-functional departments to ensure high data quality. The position operates under minimal supervision and independently evaluates, selects, and applies data management practices to a variety of research projects.
Position based at Libertyville, Illinois and requires a minimum of 3 days a week on site.
Design and Planning
Lead the development of data management sections of clinical protocol and corresponding Case Report Forms (CRFs).
Develop and maintain data management essential documentation for the Trial Master File including, but not limited to; Data Management Plan, study-specific monitoring guidelines, edit checks, and user access forms, ensuring compliance with regulatory requirements.
Support each clinical study and project team by ensuring data management plans, questionnaire development, and data handling activities are aligned to support the study objectives.
Participate in study team meetings.
EDC Administration
Design and program clinical study databases in EDC System including but not limited to CRFs, edit checks, data dictionaries, queries/alerts, and managing user roles based on the clinical protocol.
Lead User Acceptance Testing (UAT) to validate build specifications.
Train clinical research personnel on the study-specific CRF, EDC/ePRO, and other project related items as needed.
Lead database clean, lock, export, and archiving activities.
Oversee data management vendor relationships including EDC partners and CROs supporting DM tasks.
Continuously assess and enhance the EDC systems to improve efficiency and data quality.
Data Monitoring
Monitor clinical data to resolve queries and data discrepancies throughout each study according to Clinical Protocol and/or Data Management Plan.
Coordinate AE/DD reconciliation with PI.
Identify and communicate data issues and/or query trends to study team and/or management.
Assist with developing metrics on study progress and routinely report out to study team and management.
Compliance and Process
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures.
Contribute to the maintenance of GCA’s data management procedures and work instructions.
Responsible for leading or collaborating on process improvement initiatives within department.
Meet study timelines with a high degree of quality.
Other duties as needed or required.
Essential Functions of the Role
Excellent oral and written communication skills.
Strong interpersonal skills.
Demonstrated ability to work independently, as well as part of a multifunctional study team.
Ability to work on multiple concurrent studies and independently balance priorities to meet timelines.
Requirements
Number of Overall Years Necessary: 3-5
Minimum of 3 years EDC database programming and Data Monitoring experience is required.
Minimum of 2 years medical device and/or pharmaceutical clinical research experience or similar regulated industry is required.
Bachelor's degree in life sciences, computer science, or related field.
Certified Clinical Data Manager (CCDM) via SCDM or similar preferred.
Equivalent combination of education, training and work experience may be accepted in lieu of degree.
Specialized Skills/Technical Knowledge
Experience with EDC Systems (e.g. Medrio, Clinpal, Medidata Rave, etc.) required.
Understanding of clinical research regulations required.
Experience in questionnaire development, database structure, and data management processes.
Experience with Microsoft Suite Applications (Word, PowerPoint, Excel, Teams).
Knowledge relating to continence care, critical care and/or ostomy a plus.
Pay Rate Range: $50-65/hr depending on experience
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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Clinical Data Management Specialist
role at
Planet Pharma
Summary The Specialist, Clinical Data Management (CDM) is a leader in supporting clinical studies for medical device products and services. The CDM leads all aspects of clinical data management from study planning to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer. The CDM regularly collaborates with Global Clinical Affairs (GCA) study team members (Clinical Project Management, Biostatistics, Clinical Operations, Clinical Scientist) and cross-functional departments to ensure high data quality. The position operates under minimal supervision and independently evaluates, selects, and applies data management practices to a variety of research projects.
Position based at Libertyville, Illinois and requires a minimum of 3 days a week on site.
Design and Planning
Lead the development of data management sections of clinical protocol and corresponding Case Report Forms (CRFs).
Develop and maintain data management essential documentation for the Trial Master File including, but not limited to; Data Management Plan, study-specific monitoring guidelines, edit checks, and user access forms, ensuring compliance with regulatory requirements.
Support each clinical study and project team by ensuring data management plans, questionnaire development, and data handling activities are aligned to support the study objectives.
Participate in study team meetings.
EDC Administration
Design and program clinical study databases in EDC System including but not limited to CRFs, edit checks, data dictionaries, queries/alerts, and managing user roles based on the clinical protocol.
Lead User Acceptance Testing (UAT) to validate build specifications.
Train clinical research personnel on the study-specific CRF, EDC/ePRO, and other project related items as needed.
Lead database clean, lock, export, and archiving activities.
Oversee data management vendor relationships including EDC partners and CROs supporting DM tasks.
Continuously assess and enhance the EDC systems to improve efficiency and data quality.
Data Monitoring
Monitor clinical data to resolve queries and data discrepancies throughout each study according to Clinical Protocol and/or Data Management Plan.
Coordinate AE/DD reconciliation with PI.
Identify and communicate data issues and/or query trends to study team and/or management.
Assist with developing metrics on study progress and routinely report out to study team and management.
Compliance and Process
Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures.
Contribute to the maintenance of GCA’s data management procedures and work instructions.
Responsible for leading or collaborating on process improvement initiatives within department.
Meet study timelines with a high degree of quality.
Other duties as needed or required.
Essential Functions of the Role
Excellent oral and written communication skills.
Strong interpersonal skills.
Demonstrated ability to work independently, as well as part of a multifunctional study team.
Ability to work on multiple concurrent studies and independently balance priorities to meet timelines.
Requirements
Number of Overall Years Necessary: 3-5
Minimum of 3 years EDC database programming and Data Monitoring experience is required.
Minimum of 2 years medical device and/or pharmaceutical clinical research experience or similar regulated industry is required.
Bachelor's degree in life sciences, computer science, or related field.
Certified Clinical Data Manager (CCDM) via SCDM or similar preferred.
Equivalent combination of education, training and work experience may be accepted in lieu of degree.
Specialized Skills/Technical Knowledge
Experience with EDC Systems (e.g. Medrio, Clinpal, Medidata Rave, etc.) required.
Understanding of clinical research regulations required.
Experience in questionnaire development, database structure, and data management processes.
Experience with Microsoft Suite Applications (Word, PowerPoint, Excel, Teams).
Knowledge relating to continence care, critical care and/or ostomy a plus.
Pay Rate Range: $50-65/hr depending on experience
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
#J-18808-Ljbffr