Senior Medical Writer

October 1

Apply Now

Receive Emails with Similar Jobs

Parexel

WebsiteLinkedInAll Job Openings

Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Independently research, create, and edit regulatory documents of varied complexity associated with clinical research. • Project leadership experience required: primary client contact for medical writing deliverables, collaboration with Parexel or client stakeholders to plan and meet deliverable timelines and expectations in terms of process, content, quality, and team management.

Requirements

• Excellent interpersonal, verbal, and written communication skills. • Ability to understand all necessary steps in a project, plan ahead, and identify critical paths. • Efficiently manages time spent on tasks and proactively identifies deficiency. • A flexible attitude with respect to work assignments and new learning; readily adapts to changes. • Competent in a matrix environment, values teamwork and understands roles of other project team members. • Proven team leadership skills and cross-cultural sensitivity. • Exhibits sound judgement by presenting solutions or escalating issues to project teams or departmental management as appropriate. • Follows through to ensure problems have been satisfactorily resolved. • Strives to understand and satisfy client needs. • Ability to negotiate on behalf of medical writing to ensure resources, timelines and expectations are aligned. • Gains trust and establish a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services. • Provides departmental expertise and perspectives to promote prospective business opportunities. • Provides Parexel colleagues with pertinent information to formalize a sound business strategy.