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Regulatory Affairs Manager

Integrated Resources, Inc

Pennsylvania

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Brochures, Clinical Research, Communication Skills, Consulting, Content Development, Cross-Functional, Data Analysis, Detail Oriented, Documentation, Drug Development, FDA (Food and Drug Administration), FDA Requirements, Healthcare, ICH Regulations, Information Technology & Information Systems, Investigational New Drug (IND), Maintain Compliance, Medical Products, Meeting Minutes, Multitasking, Operations Management, Organizational Skills, Plan Meetings, Policy Implementation, Presentation/Verbal Skills, Problem Solving Skills, Product Development, Project/Program Management, Quality Control, Regulations, Regulatory Requirements, Regulatory Submissions, Rehabilitation Nursing, Research Protocols, Scientific Principles, Team Lead/Manager, Team Player, Writing Skills
LOCATION
Pennsylvania
POSTED
2 days ago
Regulatory Affairs ManagerA 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 position is with my direct clientJob DescriptionPosition Details:Client Direct ClientLocation Wayne, PAJob Title Regulatory Affairs ManagerDuration 6 Months+Must have skill-set [Job Description] Job Summary:Responsible for the management and conduct of US regional regulatory activities as directed by and under supervision of manager. Lead regulatory activities for assigned projects in line with US regulatory requirements.Primary Responsibilities Include:•With supervision as appropriate, function as liaison between FDA and company for assigned projects.•The planning, coordination, organization and preparation of complete high quality regulatory submissions for assigned products, including both pre-approval and postmarketing submissions.•Ensuring regulatory compliance for all assigned responsibilites.•Responsible for the implemention of regulatory strategies for the development and maintenance of assigned product or products.•Maintain up-to-date knowledge and expertise of FDA regulations/guidance documents, and ICH guidelinesResponsibilities:- Prepare, compile, review/qualilty control and process regulatory submissions including INDs, BLA, NDA, amendments/supplements, annual reports, study protocols, study reports, investigator brochures, safety reports, etc.- Attend and participate in assigned project/regulatory product development and submission teams, providing clear and consistent regulatory recommendations.- Coordinate and consult with other departments on the content, quality and assembly of regulatory documentation. Ensure consistency, completeness and adherece to standards for all regulatory submissions.- Conduct regulatory communications with FDA, under appropriate supervision and direction, for assigned products and activities.- Coordinate FDA meeting requests, meeting rehearsals, briefing book preparations and preparing meeting minutes of FDA meetings.QualificationsEducation and Experience:BA/B.S in a scientific, healthcare or related field or equivalent experience. Advanced degree preferred, but not required•5 -10 years of biopharmaceutical experience with emphasis in regulatory affairs and drug development•Knowledge of FDA regulations and guidelines on drug development and the approval process for NDA/BLA and postmarketing supplements•Strong written/verbal communication skillsKey Skills:•Excellent communication skills both written and verbal•Demonstrates strong ability to collaboratively interact and work effectively with other departments as well as external organiations•Excellent organizational skills, ability to multitask and with attention to detail; capable of managing multiple projects within assigned timelines•Ability to apply scientific principles to assess regulatory issues, request and collect relevant information, analyze data, establish facts and draw valid conclusionsComplexity and Problem Solving:•Under supervision of regulatory management and in conjunction with cross functional team members execute regulatory strategies, develop submission timelines and content plans for regulatory submissions.•Contribute to the development of specific regulatory content supporting company positions as presented in required regulatory documents.Internal and External Contacts:•With supervision function as liaison between FDA and company for assigned projects.•Consults with regulatory management and Global Regulatory Leads on product team related issues, planning and submissions;•Represents the US strategy regulatory group as well as GRA on assigned product teams including clinical operational study management teams.•Interacts with cross functional team members, e.g. clinical operations, nonclinical development on development program related issues;•Works with regulatory operations on the development of regulatory submissions.Feel free to forward my email to your friends/colleagues who might be availableAdditional InformationThanks!!!Warm Regards,Amrit SinghClinical RecruiterIntegrated Resources, IncIT REHAB CLINICAL NURSINGTel: (732) 429 1634Fax: (732) 549 5549

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Integrated Resources, Inc