Senior Medical Writer (GSK)

Roles and Responsibilities

Responsibilities

• Actively participates in document planning and review meetings.

• Demonstrates understanding of how to interpret and describe clinical data

• Raises and discusses concerns/ issues in an open and timely manner within the global Medical Writing Team

• Promotes high medical writing standards by pointing out obvious flaws and proposing alternatives.

• Actively participates in document planning and review meetings.

• Raises and discusses concerns/ issues in an open and timely manner within the global team at GSK

• Establishes network of communication and continuously builds these relationships with stakeholders to facilitate efficient execution of assignment.

• Has ability to interpret, describe and document clinical data and discuss with team.

• Promotes high medical writing standards by pointing out obvious flaws and proposing alternatives

Basic Qualification

• Up to 5 years clinical regulatory writing experience in the pharmaceutical industry

• Possesses a good understanding of basic drug development

• Demonstrates knowledge of scientific methodology and statistical principles in the design, conduct and description of clinical research.

• Demonstrates understanding of how to interpret, describe and document clinical data.

• Possesses working knowledge of International Committee for Harmonisation (ICH) / Good Clinical Practice (GCP).

• Possesses necessary computer skills and general computer literacy.

• Excellent English language skills (verbal and written)