About the job

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 with enthusiasm and prioritize workload with attention to detail, e.g.,

organizational skills.

• Willingness to work in a matrix environment, values the importance of teamwork,

and understands roles of other project team members.

• Strives to understand and satisfy client needs.

Demonstrated understanding of clinical research, the drug development process, and industry

guidelines and regulations, e.g., ICH-GCP.

• Good clinical/scientific writing skills.
• Scientific background essential; writing experience of regulatory documents such as patient

narratives, informed consent forms or similar in a contract research organization, pharmaceutical

or biotechnology firm, or some experience in the conduct of clinical research/medical

communications.

• Good word processing skills, including MS Office (proficiency 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.

• If required to perform translation work and quality control of documents written in non-English

language, proficiency in relevant language is a prerequisite.

Qualifications

• Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent.

Apply through this Link