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Senior Medical Writer, Scientific and Medical Services

Parexel International Corporation

Nottingham, England, United Kingdom

The Senior Medical Writer will research, create, and edit all documents related to the independent review, including independent review charters, clinical data forms, manual case report forms, applicable reviewer training materials, project deviations, and supplemental imaging reports using all available central content and templates.

Responsibilities also include:acting as primary client contact for medical writing projectsworking closely with other Parexel departments and clients to set and meet internal/external deliverable timelinesproject leadershiptraining and support of junior medical writing staff, potentially including line management.Qualifications• Excellent interpersonal, verbal, and written communication skills.

• Ability to consistently produce documents of high quality.

• Demonstrates attention to details and proactivity.

• Ability to understand all necessary steps in a project, plan ahead, and identify critical paths.

• A flexible attitude with respect to work assignments and new learning; readily adapts to changes.

• Ability to efficiently manage time spent on tasks and proactively identify deficiency.

• Manage multiple and varied tasks and prioritize workload with attention to detail.

• Competent working in a matrix environment and values the importance of team work.

• Possesses team leadership skills and cross-cultural sensitivity.

• Ability to negotiate on behalf of medical writing to ensure resources, timelines, and expectations are aligned.

• Gains trust and establishes a connection with the client beyond one’s project, to gain repeat business and/or to widen existing scope of services.

• Provides departmental expertise and perspectives to promote prospective business opportunities

• Provides Parexel colleagues with pertinent information to formalize a sound business strategy.

Knowledge and Experience:

• Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, i.e., ICH-GCP.

• Extensive clinical/scientific writing skills.

• Scientific background essential; writing experience includes all clinical documents related to the independent review.

• Advanced word processing skills, including MS office (expertise in Word); software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel).

• Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation.

Education:

• Educated to degree level (biological science, pharmacy or other health-related discipline preferred), nursing or other relevant qualification/experience.

Job posted: 2020-11-27

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