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Project Coordinator

Integrated Resources, Inc

Raynham, Massachusetts

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biology, Business Practices, Calendar Management, Clinical Assessment, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Communication Skills, Corporate Compliance, Corporate Policies, Information Technology & Information Systems, Leadership, Maintain Compliance, Medical Affairs, Medical Equipment, Medical Office Administration, Medical Writing, Microsoft Office, Multitasking, Organizational Skills, Presentation/Verbal Skills, Product Documentation, Project Management Professional (PMP), Project/Program Coordination, Regulations, Regulatory Compliance, Regulatory Requirements, Rehabilitation Nursing, Safety Compliance, Safety/Work Safety, Time Management, Vendor/Supplier Management, Writing Skills
LOCATION
Raynham, Massachusetts
POSTED
2 days ago
Project CoordinatorA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionPOSITION SUMMARY:This individual will primarily support Medical Affairs in the coordination of Clinical Evaluation Reports (CER) across DePuy Synthes. This may entail scheduling CER Review meetings, tracking CER timelines, vendor management, and tracking literature search requests to ensure CER timelines are met.JOB RESPONSIBILITIES:• Ensure that safety and efficacy of our products are documented, processed, and reported following Company guidelines, internal business practices, and regulatory guidance to ensure compliance with worldwide safety regulations and corporate policies.• Administrative Leadership• Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance.QualificationsEDUCATION:• BS in Life Sciences, PMP preferredKnowledge/Requirements:• This is an entry level position• Broad knowledge of medical device clinical and regulatory requirements is preferred.Additional Requirements:• Strong skills and demonstrated competencies in the following areas are required:• Verbal and written communication skills• Proven ability to multi-task• Effective time management skills• Strong organizational skills• Proficiency with the Microsoft Office suite• Medical writing and presentation skills

About the Company

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Integrated Resources, Inc