job title: Medical writer(syngene)

Roles and Responsibilities

• Independently develop and finalize clinical and scientific documents for different regulatory submissions such as (but not limited to) Bioanalytical reports, Clinical Study Reports (CSRs), part of Electronic Common Technical Document (eCTD) modules, covering various therapeutic areas, and phases of clinical research

• Collaborates with internal and external clients to support and enable effective communication resulting in operational excellence

• Effectively manages medical writing and review processes to deliver quality projects in agreed timelines

• Ensure compliance to applicable regulatory guidelines, department SOPs, client style guides, conventions as applicable

• Ensures that appropriate documented quality control (QC) checks are performed on medical writing deliverables and responds to findings

• Follow any other instructions and perform any other related duties, as assigned by the supervisor.

• Performs literature search/review as necessary to obtain background information for developing scientific content

Educational Qualification:

• Graduate in Life Sciences

• Masters in Life Science

Experience:

2-4 Years

Behavioural Skills:

• Good communication

• Quick learner

• Adapt to change

• Time management

• Professionalism

Technical/functional Skills:
• Ability to comprehend scientific information
• Good understanding of clinical research.
• Knowledge of working on MS word, PPT etc.
• Attend training on environment, health, and safety (EHS) measures imparted company