System One Holdings, LLC
Data Manager
System One Holdings, LLC, Tarrytown, New York, United States, 10591
Title: Clinical Data ManagerLocation:RemoteDuration:6 month renewableDM Experience:5 years (CRO Experience is ok) - This is NOT a lead role.
**We cannot work C2C with any other agency for this position.**
Are you a Clinical Data Manager who is ready to take on your next challenge?Have you been working as a Clinical Data Manager at a CRO and are interested in moving to a sponsor?We have an exciting Data Manager opportunity available with a global sponsor client, who is leading the way with innovative new medicines for the treatment of serious diseases.If you are interested, apply today!
The Clinical Data Manager will work collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and according to study protocol and the Study Data Management Manual (DMM). Works with involved parties to assure that DMM is prepared according to company SOPs and in compliance with company's data standards. Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's SOPs and policies and practices.
A typical might include the following:
•Serves as primary DM contact for assigned studies, including representation on project teams and working with CROs performing data management tasks for assigned study.•Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's SOPs and policies and practices including, not limited to:o Monitors data clean-up process performed by CROs from study start-up through data archiving.o Provides data for analysis.o Coordinates activities including: medical coding; data validation checks and database snapshot.•Prepares and distributes project status reports to project team and management.•Functions as DM team leader responsible for ensuring databases are validated and ready for transfer and/or analyses in accordance with client SOPs.•Creates and maintains project documentation, including, but not limited to, Data Management Manual, CRF Completion Guidelines and validation specifications, and work instructions for assigned projects.Designs and modifies CRF.•Responsible for the initiation and approval of the building, testing and validation of clinical databases, subsequent changes in clinical databases and data validation activities.
This Job Might Be for You If You:
Have a passion for championing and implementing clinical data platform.Enjoy working in an innovative and multi-functional team.Have strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.Possess Excellent communication, and project management skills.
To be considered for this role you must have:
Bachelor's degree in Mathematics, Science or a related field, along with 5+ or more years of clinical data management experience in biotechnology, pharmaceutical or health related industry.
**We cannot work C2C with any other agency for this position.**
Are you a Clinical Data Manager who is ready to take on your next challenge?Have you been working as a Clinical Data Manager at a CRO and are interested in moving to a sponsor?We have an exciting Data Manager opportunity available with a global sponsor client, who is leading the way with innovative new medicines for the treatment of serious diseases.If you are interested, apply today!
The Clinical Data Manager will work collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and according to study protocol and the Study Data Management Manual (DMM). Works with involved parties to assure that DMM is prepared according to company SOPs and in compliance with company's data standards. Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's SOPs and policies and practices.
A typical might include the following:
•Serves as primary DM contact for assigned studies, including representation on project teams and working with CROs performing data management tasks for assigned study.•Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's SOPs and policies and practices including, not limited to:o Monitors data clean-up process performed by CROs from study start-up through data archiving.o Provides data for analysis.o Coordinates activities including: medical coding; data validation checks and database snapshot.•Prepares and distributes project status reports to project team and management.•Functions as DM team leader responsible for ensuring databases are validated and ready for transfer and/or analyses in accordance with client SOPs.•Creates and maintains project documentation, including, but not limited to, Data Management Manual, CRF Completion Guidelines and validation specifications, and work instructions for assigned projects.Designs and modifies CRF.•Responsible for the initiation and approval of the building, testing and validation of clinical databases, subsequent changes in clinical databases and data validation activities.
This Job Might Be for You If You:
Have a passion for championing and implementing clinical data platform.Enjoy working in an innovative and multi-functional team.Have strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.Possess Excellent communication, and project management skills.
To be considered for this role you must have:
Bachelor's degree in Mathematics, Science or a related field, along with 5+ or more years of clinical data management experience in biotechnology, pharmaceutical or health related industry.