Manager, Clinical Data Management in a CRO - Full Time REMOTE, some travel
Job Description:
Job Description / Summary
The Manager, Clinical Data Management is a full-time exempt position reporting to the Director, Clinical Data Management.
PLEASE NOTE: Candidates must have a valid Green Card or U.S. citizenship. No visa sponsorship is available now or in the future.
Must Have
⢠12+ years of hands-on data management experience.
⢠6-7 years of managerial experience, managing a team of at least 5 people.
⢠4+ years of experience in the CRO environment.
⢠Excellent oral and written communication skills.
⢠Ability to work in the PST time zone (flexible).
⢠Willingness to travel 2-3 times a year when necessary.
Responsibilities
⢠Provide data management expertise to project teams, clients, and CROs, including study startup documents, data cleaning, DCF/query tracking, database QC, and SAE/AE reconciliation.
⢠Oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and User Acceptance Testing.
⢠Conduct cross-functional data reviews, identify issues, and track resolutions.
⢠Innovate and implement new technologies for process improvements.
⢠Ensure adherence to quality control procedures.
⢠Write and update SOPs/training guidelines.
⢠Facilitate internal study team, client, and CRO meetings.
⢠Review study data quality, provide metrics, and report out-of-scope activities.
⢠Manage timelines and resources to meet deadlines.
⢠Identify and recommend solutions for process inefficiencies.
⢠Assist in preparing proposals and budgets for new and ongoing projects.
⢠Direct and manage team members, including training, resource assignment, and performance reviews.
Education and Experience Requirements
⢠12 years of hands-on data management experience.
⢠6-7 years of managerial experience, managing a team of 5+ people.
⢠B.S./B.A. in a science or technical discipline with 8 years of data management experience, or MS degree with 6 years of data management experience; minimum 4 years in the Pharmaceutical/Biotechnology industry or CRO environment.
⢠Proficiency in SQL or SAS is desirable but not required.
⢠Experience with various data collection and EDC systems.
Knowledge & Skills Requirements
⢠Excellent oral and written communication skills.
⢠Ability to work collaboratively in a multi-disciplinary environment.
⢠Good knowledge of FDA, EMA, ICH guidelines, and GCPs, especially related to data handling and processing.
Salary and Benefits
⢠Market rate compensation as base salary with all the benefits.
Required Skills:
⢠Biotechnology
⢠Data Cleaning
⢠Project Teams
⢠Data Quality
⢠SAS
⢠User Acceptance Testing
⢠Resolutions
⢠Data Collection
⢠Data Management
⢠Salary
⢠Checks
⢠Communication Skills
⢠Compensation
⢠Timelines
⢠Reviews
⢠Metrics
⢠Travel
⢠Quality Control
⢠Specifications
⢠Education
⢠Testing
⢠SQL
⢠Science
⢠Training
⢠Communication
⢠Management
Apply tot his job
Apply To this Job
Job Description / Summary
The Manager, Clinical Data Management is a full-time exempt position reporting to the Director, Clinical Data Management.
PLEASE NOTE: Candidates must have a valid Green Card or U.S. citizenship. No visa sponsorship is available now or in the future.
Must Have
⢠12+ years of hands-on data management experience.
⢠6-7 years of managerial experience, managing a team of at least 5 people.
⢠4+ years of experience in the CRO environment.
⢠Excellent oral and written communication skills.
⢠Ability to work in the PST time zone (flexible).
⢠Willingness to travel 2-3 times a year when necessary.
Responsibilities
⢠Provide data management expertise to project teams, clients, and CROs, including study startup documents, data cleaning, DCF/query tracking, database QC, and SAE/AE reconciliation.
⢠Oversee development of specifications for eCRFs/CRF, edit checks, electronic data handling, manual review, and User Acceptance Testing.
⢠Conduct cross-functional data reviews, identify issues, and track resolutions.
⢠Innovate and implement new technologies for process improvements.
⢠Ensure adherence to quality control procedures.
⢠Write and update SOPs/training guidelines.
⢠Facilitate internal study team, client, and CRO meetings.
⢠Review study data quality, provide metrics, and report out-of-scope activities.
⢠Manage timelines and resources to meet deadlines.
⢠Identify and recommend solutions for process inefficiencies.
⢠Assist in preparing proposals and budgets for new and ongoing projects.
⢠Direct and manage team members, including training, resource assignment, and performance reviews.
Education and Experience Requirements
⢠12 years of hands-on data management experience.
⢠6-7 years of managerial experience, managing a team of 5+ people.
⢠B.S./B.A. in a science or technical discipline with 8 years of data management experience, or MS degree with 6 years of data management experience; minimum 4 years in the Pharmaceutical/Biotechnology industry or CRO environment.
⢠Proficiency in SQL or SAS is desirable but not required.
⢠Experience with various data collection and EDC systems.
Knowledge & Skills Requirements
⢠Excellent oral and written communication skills.
⢠Ability to work collaboratively in a multi-disciplinary environment.
⢠Good knowledge of FDA, EMA, ICH guidelines, and GCPs, especially related to data handling and processing.
Salary and Benefits
⢠Market rate compensation as base salary with all the benefits.
Required Skills:
⢠Biotechnology
⢠Data Cleaning
⢠Project Teams
⢠Data Quality
⢠SAS
⢠User Acceptance Testing
⢠Resolutions
⢠Data Collection
⢠Data Management
⢠Salary
⢠Checks
⢠Communication Skills
⢠Compensation
⢠Timelines
⢠Reviews
⢠Metrics
⢠Travel
⢠Quality Control
⢠Specifications
⢠Education
⢠Testing
⢠SQL
⢠Science
⢠Training
⢠Communication
⢠Management
Apply tot his job
Apply To this Job