Location/Division Specific Information
#CorEvitas
Discover Impactful Work:
As a member of the Clinical Data Management (CDM) team, the Associate Clinical Data Manager is responsible for the day-to-day registry data activities. Those activities include, but are not limited to: reviewing data, issuing/resolving queries, attending registry meetings, creating/maintaining documentation, and raising risks.
A day in the Life:
• Responsible for reviewing data on assigned registries to ensure timeliness, completeness, and quality. Issuing and resolving queries as appropriate and applicable.
• Provide input, assistance, and/or oversight for relevant data management documentation such as Completion Guidelines, Data Management Plan as well as edit check specifications.
• Assist with the creation of test data for entry screens and edit checks. Perform UAT for new registry builds as well as for mid-study updates (MSUs), as needed.
• Attend and/or participate in registry meetings for assigned registries as well as attend the monthly PMO meetings.
• Collaborate with respective registry leads and/or stakeholders to provide registry data updates, cleanliness, risks and mitigation plans, and metrics.
• Participate in and/or contribute to any internal and/or external Regulatory audits and/or inspections, as applicable.
• Perform other duties as required by the Department.
Keys to Success:
Education
Bachelor's degree, or equivalent experience in lieu of degree
Experience
• Prior experience in the pharmaceutical, biotechnology, medical device/diagnostics, or clinical trial industries.
• Minimum of 1 years' experience in Clinical Data Management, or related experience.
Knowledge, Skills, Abilities
• Ability to maintain confidentiality of data and information during interactions with staff at all levels.
• Effective communication and writing skills.
• Strong attention to detail and ability to multitask.
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