Senior ICF Medical Writing Project Manager

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profile Job Location:

Mumbai - India

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Second Shift (Afternoons)

Environmental Conditions

Office

Job Description

Purpose:

Leads patient-centric medical writing projects with a primary focus on Informed Consent Forms (ICFs) through collaboration with internal and client teams. Manages project timelines budgets and resources. Manages and ensures the timely delivery and the quality of individual projects and documents for internal and external clients. Builds client relationships and identifies and resolves client management issues. Develops monitors and adapts project plans timelines and budgets/forecasting for assigned projects.

Essential Functions:

  • Develops project timelines standards budgets forecasts and contract modifications for assigned projects. Serves as liaison with other departments on contract modifications.

  • Collaborates with cross-functional team members as needed to meet the deliverables of the project. Regularly communicates with the team and leads team meetings to ensure that timelines resources and quality are maintained.

  • Ensures achievement of final deliverables within the contractual time period by preparing and monitoring timelines providing status updates to the appropriate point of escalation and regularly reviewing projects using tracking and management tools.

  • Evaluates and appropriately escalates or resolves risks to project quality budget or timeline.

  • Ensures compliance with quality processes and requirements for assigned projects both within and between documents within a project. Reviews and manages performance metrics for assigned projects.

Qualifications:

Education and Experience:

BS/BA (scientific discipline preferred) with at least 5 years relevant experience or an advanced degree with at least 3 years relevant experience

Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 5 years).

Experience in managing medical writing or clinical projects required.

Experience working in the pharmaceutical/CRO industry preferred.

Experience in medical writing (eg Regulatory and/or plain language) advantageous.

Years of experience refers to typical years of related experience needed to gain the required knowledge skills and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge Skills and Abilities:

Strong project management skills to include budgeting forecasting and resource management.

Solid planning and organizational skills to enable effective prioritization of workload.

Excellent interpersonal skills including problem solving judgment and decision-making skills; self-motivated and adaptable

Effective oral and written communication skills with internal and external stakeholders; strong negotiation skills

Good knowledge of global regional national and other regulatory and document development guidelines relevant to patient-centric deliverables.

Good judgment; high degree of independence in decision making and problem solvi


Required Experience:

Senior IC

Work ScheduleSecond Shift (Afternoons)Environmental ConditionsOfficeJob DescriptionPurpose:Leads patient-centric medical writing projects with a primary focus on Informed Consent Forms (ICFs) through collaboration with internal and client teams. Manages project timelines budgets and resources. Manag...
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Key Skills

  • Business Development
  • Project Management Methodology
  • Project / Program Management
  • PMBOK
  • Waterfall
  • Wastewater
  • Construction Management
  • Project Management
  • Project Management Software
  • Microsoft Project
  • Budgeting
  • Contracts

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