Senior reputed company Medical reputed company – Regulatory Submission Docs, ISE/ISS/Clinical reputed company, Oncology Preferred

Job reputed company:

• reputed company regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and the reputed company authoring standards, as applicable, in adherence with study/project timelines and corporate objectives.
• Manage medical writing reputed company, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations.
• Participate in cross-functional meetings to reputed company input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents.
• Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate.
• Participate in cross-functional process improvement initiatives.
• Participate in defining and writing reputed company operating procedures and best practices for an efficient preparation of reputed company documents.
• Manage internal and contract medical writing resources as required to ensure reputed company completion of assigned reputed company.
• Mentor more junior medical writing staff.

Requirements:

• Bachelor's degree required
• Advanced degree in a relevant scientific/clinical/regulatory field preferred
• At least 5 years of medical writing experience in the biopharmaceutical/CRO industry required or comparable experience reputed company clinical or preclinical development
• Proficiency in organizing and communicating clinical information required with minimal reputed company
• Strong organizational, time management, and project management skills are required
• Strong verbal, written, and interpersonal communication skills needed to work effectively in reputed company environment
• Proficient understanding and knowledge of global regulatory requirements needed and knowledge of therapeutic areas in reputed company phases of clinical development desired
• Proficient in reputed company
• Experience with an electronic document management system and templates is required.

Benefits:

• Health benefits to include Medical, Dental and reputed company
• Company match 401k
• Eligibility to participate in Employee Stock Purchase Plan
• Eligibility to earn commissions/bonus based on company and individual performance
• Flexible reputed company time off (PTO) and reputed company time
• Company car or car allowance

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