Job Description:

Responsibilities

• Reviews literature articles and extracts relevant information

• Highly knowledgeable and experienced in the regulatory medical writing process

• Suggests or identifies modifications, changes, and improvements to the document preparation procedures and templates in order to improve efficiency, quality, and productivity

• Provides a structured focus for writing content (task, concept, reference, and troubleshooting)

• Creates and maintains standard operating procedures and work instructions for preparation and maintenance of compliant medical writing deliverables

• Ensures that appropriate documented quality control checks are performed on medical writing deliverables and recommends process improvements

• Enhances the quality of clinical documentation through reasoning and presentation

• Facilitates technical discussions with clinical evaluators and customer therapeutic area experts

Provides training to the medical writing team related to process, amendments, and recent market updates

Contract length: 6 months

Job Types: Full-time, Contract

Salary: From 25.00? per month

Experience:

• Medical writing: 5 years (Required)
• post marketing report: 4 years (Required)
• Clinical Evaluation Report(CER): 4 years (Required)

Work Remotely:

• Yes