Program Mgr Med Writing Remote Based
Canada, Canada
Job Description
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Summarized Purpose: Unique opportunity as a dedicated program manager within a clinical phase medical writing group. Leverages experience as a medical writer to serve as a subject matter expert for medical writing deliverables. Works with a diverse client base with exposure to a variety of therapeutic areas, indications, and therapeutic innovations. Leads client programs with prominent visibility among internal and client teams, with a high degree of client engagement and management. Manages client relationships and identifies and resolves client management issues. Manages and ensures the quality and timely delivery of multiple program documents. Collaboratively resources projects and leads writing teams in a matrix management environment. Develops, monitors, and adapts project plans, client and program-specific processes, timelines, and budgets/forecasting for programs. Essential Functions:
- Develops project timelines, standards, budgets, forecasts and contract modifications for assigned projects.
- Serves as point of contact for risk escalation for assigned programs. Evaluates and appropriately escalates or resolves risks to project quality, budget, or timeline.
- Ensures compliance with quality processes and requirements for assigned programs both within and between documents within a project. Develops, reviews, and manages performance metrics for assigned projects.
- Provides training for medical writers on scientific content of medical writing deliverables, medical writing best practices, and technical aspects of program management.
- May serve as backup medical writer
- Bachelor\'s degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
- Experience in managing and directing complex medical writing projects required
- Experience working in the pharmaceutical/CRO industry preferred
- Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous
- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Solid program management skills to include budgeting, forecasting and resource management
- Extensive knowledge of global, regional, national and other document development guidelines
- In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications, etc.
- Excellent interpersonal, oral and written communication, and presentation skills
- Excellent negotiation skills
- Self-motivated and adaptable
- Excellent judgment; high degree of independence in decision making and problem solving
- Capable of mentoring and leading junior level staff
- Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
- Able to work upright and stationary for typical working hours.
- Ability to use and learn standard office equipment and technology with proficiency.
- Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
- May require travel. (Recruiter will provide more details.)
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Job Detail
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Job IdJD2147002
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationCanada, Canada
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EducationNot mentioned