Medical Writer

As a Medical Writer you will ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally. Furthermore, you will communicate across the time zones and in different professional environments.

 This job requires good communication and analytical skills. In order to meet timelines, you must be good at planning own work and be proactive when problems arise and seek help and advice from relevant people within GBS as well as within Head Quarters (HQ). Additionally, you will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved. You are entrusted to fulfill the following responsibilities:

• You will be performing medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports (CTRs), Non-interventional study reports (NSRs), Layperson Summary (LPS), Investigator Brochure (IB) and Regulatory response documents (QA).

• You will have to communicate the clinical data in a clear and concise manner.

• You will contribute to knowledge sharing and maintain good relationship with the stakeholders and colleagues.

Qualification

You are expected to have the below skills and knowledge:

• Graduate (PhD, MSc., M Pharm, or equivalent).

• 4+ years of experience as medical writer or other relevant work experience.

• Experience working within a global setting.

• Experience from the pharmaceutical /CRO industry.

• Strong understanding of external requirements related to regulatory documents.

• Good communication skills.

• Works independently on smaller tasks.

• Strong analytical skills.

• Committed, persistent and accountable.

• Able to plan and manage variable workload.