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Project coordinator

Integrated Resources, Inc

Raynham, Massachusetts

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JOB DETAILS
JOB TYPE
Contractor
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, Maintain Compliance, Medical Affairs, Medical Equipment, Medical Office Administration, Microsoft Office, 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.This is Direct Hire Position with one of our Clients (7 to 10 Years of Total Experience)Job DescriptionJob Responsibilities: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.Business LeadershipEnsure 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 LeadershipEnsure 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 skillsProven ability to multi-taskEffective time management skillsStrong organizational skillsProficiency with the Microsoft Office suiteMedical writing and presentation skillsJob LocationI'm interested

About the Company

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Integrated Resources, Inc