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Medical Records Jobs in New Jersey

Medical Writer

Integrated Resources, Inc

Madison, New Jersey

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Academic Background, Analysis Skills, Biotech and Pharmaceutical, Clinical Data, Clinical Practices/Protocols, Clinical Research, Clinical Study Publications, Communication Skills, Cross-Functional, Datasheets, Drug Development, Drug Products, Establish Priorities, ICH Regulations, Information Technology & Information Systems, Leadership, Literacy, Marketing, Medical Writing, Mentoring, Pharmacology, Presentation/Verbal Skills, Process Improvement, Project/Program Management, Regulations, Regulatory Reports, Rehabilitation Nursing, Requirements Management, Risk, Risk Management, Standard Operating Procedures (SOP), Strategic Planning, Team Lead/Manager, Technical Presentation, Technical Writing, Time Management, Writing Skills
LOCATION
Madison, New Jersey
POSTED
1 day ago
Medical WriterA 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 ClientsJob DescriptionThe author will provide medical documentation summarizing risks and benefits in support of the development, license application and approval, and post-marketing development of one or more drug products. This will be achieved by applying analytical skills, functional literacy and expertise in document preparation. The author will contribute essential deliverables which could include clinical overviews, integrated analyses of safety and efficacy, responses to regulatory questions, risk management plans, REMS, key sections of the Investigator's Brochure, the Annual Safety Report and regulatory briefing documents. Individual will create and foster an environment of partnership with other members of product teams, in collaboration with the Project Team, assess document requirements, complexity, and potential issues with a submission, and develop strategies to deal with these, and lead a team of internal and external (contractors) authors.Responsibilities:Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and biotherapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products.For submissions, ensure high quality written presentations of Common Technical Document Efficacy components that are compliant with regulations, ICH guidelines, and corporate SOPs.Author documents such as agency briefing documents, key sections of the Investigator's Brochure, the Annual Safety Report and the core data sheet.Communicate resource, timeline and emerging data interpretation issues that have regulatory impact, to the project team and line management.Develop and sustain constructive relationships within WSR, and with Development Operations.Collaborate with development Product Teams to prepare or lead preparation of Clinical/Regulatory documents (MD deliverables).Identify resource, timeline and emerging data interpretation issues that have regulatory impact, and clearly communicate the consequences of these issues to the project team and line management.Serve as the point of contact ("go to" person) for one or more projects or products.Organize and lead a MD matrix team of authors to deliver all MDL deliverables for each assigned project.Ensure key messages and document style are communicated to authors and team to ensure consistency across different documentsTechnical Skill Requirements:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy.Able to think creatively and to develop strategic plans that demonstrate sound judgment.Exhibits sound project management and time management skills.Able to interact effectively with all levels/roles of project team members.Able to manage expectations and the time pressures associated with authoring, resolving comments, updating and finalizing documents.Demonstrates proactive nature in taking on assignments and readily mentors other colleagues in area of expertise.Is able to implement systems and processes and suggest process improvements.Able to project manage and appropriately prioritize medium to high volume of work, with short deadlines.Able to complete and turn around high quality outputs with only minimal guidance from managementQualificationsScientific/medical academic background (e.g. PharmD/PhD or MSc/BSc with experience), or equivalent. BS degree and 1 or more years of pharmaceutical experience preferred. An advanced degree preferred and at least 3 years medical writing experience and/or experience in pharmaceutical development. Strong functional literacy is desirable: for example a track record of communicating complex information and analyses effectively in writing to a variety of scientific and non-scientific audiences. Applies expert knowledge, analytical skills, and knowledge of clinical and regulatory guidance. Able to clearly articulate scientific and clinical data in all written and verbal communication. May include a track record of leadership abilities either as a direct supervisor or within a matrix setting

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