Clinical Data Manager
Location:  Fully Remote
Term:  6 month - renewable
$60-70/hour (depending on experience)
NO oversight experience required.

Must haves: 
Education: Bachelor’s degree in Mathematics, Science or a related field. Must have at least 3years of DM clinical data management experience in biotechnology, pharmaceutical or health related industry. Previous oncology and/or ophthalmology experience a plus.

SUMMARY:
Works 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 company's SOPs and policies and practices.

JOB RESPONSIBILITIES:

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 company's SOPs and policies and practices including, not limited to:  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 company 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.

Contributes to upkeep DM outsourcing strategies and long-term relationships with outsourcing partners with objective of ensuring data quality and efficiencies through data and process standardization.

Works with study team and coordinates all data management functions. Manages coordination of CRO data manager and project team to ensure that tasks are performed according to policies and procedures.

JOB REQUIREMENTS:
Education:
• Bachelor’s degree in Mathematics, Science or a related field, along with 3 or more years of clinical data management experience in biotechnology, pharmaceutical or health related industry.

Experience:
• 3 – 5 Years
• Previous oncology and/or ophthalmology experience a plus

System One, and its subsidiaries including Joulé, ALTA IT Services, TeamPeople, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.