Project Coordinator (Data Governance)

Full Time Contract with possibility of Right to Hire Title or Role: Project Coordinator (Compliance / Data Governance)Compensation: up to $45/hour - commensurate with experienceLocation: Rensselaer, NYLength of Contract: 1 YearPosition DescriptionRCM is seeking a motivated individual that is "willing to learn". The individual will act as a Project Coordinator providing support to the Data Governance Program Management Team. Will assist with tasks that maintain the Data Governance Program.The Consultant provides support of quality system records activities such as the creation of approval of change controls, risk assessments, corrective and prevention action plans (CAPAs) standard operating procedure (SOPs), work instructions/job aids, policies, process quality deviations etc.This is a phenomenal opportunity to join a Biotechnology giant that is looking for that special person to mentor and help grow the Data Governance Team. Willingness to learn!!!!Job Responsibilities: include, but are not limited to, the following:Organize and schedule meetings with various departments and teamsMaintain distribution lists to ease communicationProduce and distribute meeting minutes, as required, obtain feedbackPrepare and maintain monthly metric based on quality system dataCreate monthly PowerPoint presentations for review by Data Governance Program Management TeamCoordinate document workflows to support certain Quality EventsCoordinate and route incoming questions related to Data IntegrityUpdate and maintain SharePoint pages used by The Data Governance Program Management TeamQualifications:1-3 years of experience working in an FDA regulated environmentMUST DEMONSTRATE WILLINGNESS TO LEARN!!!Experience with quality management systems including change control, incident management, and deviation management.Project Coordinator experience leading efforts requiring coordination between cross-functional teams within at least one area of systems validation - (e.g., laboratory equipment, facilities, utilities, manufacturing equipment, information systems, etc.)Continuously drive to improve processes for improved performanceExcellent Technical writing and communication skillsExcellent analytical and problem-solving skillsBasic knowledge of FDA CFRs, Eudralex, and other biotech pharma industry regulations (pertaining to IT, laboratory systems, automation, and manufacturing)Education & CertificationsBachelor's degree in a relevant field (e.g., Computer Science, Engineering, Information Technology) preferred.Equal Opportunity StatementRCM is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.Pay TransparencyRCM believes in transparency and fairness in compensation. We are committed to providing our employees with competitive salaries that reflect their skills, experience, and contributions to our organization. As part of our commitment to pay transparency, we want to provide you with as much information as possible about our compensation practices.DisclaimerThis job posting is intended to describe the general nature and the level of the work to be performed. It is not intended to include every job, duty and responsibility specific to the position. RCM reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.About RCMRCM is a leading provider of Business, IT, and Engineering Services to over 1,000 clients in the commercial marketplace including. RCM partners with clients to define, implement and manage a broad range of technologies across multiple platforms, systems, and networks. Our broad geographic presence ensures that a proven and reliable tactical and strategic capability is available and deployable virtually everywhere in North America.