A career with Kinapse means your everyday work improves patients’ lives around the world. We are a values driven company with a supportive and flexible culture. You will work in a collaborative environment with team members who share their expertise and knowledge. Your personal and professional development will be front and center. We can offer you a fulfilling and challenging career working with smart, yet humble professionals. We reward and recognise our people by providing valuable benefits and a quality of life balance.

Senior Associate CTD

Updated: August 26, 2021
Location: Bengaluru, KA, India
Job ID: 134050

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Role Purpose/Key Responsibilities:

•           Undertakes project specific activities at high quality and in defined timelines according to standard processes and operating procedures

•           Authoring and/or editing of pertinent documents such as:

o          Clinical study documents or documents for regulatory submission i.e., clinical study reports, patient narratives, clinical summaries etc.

o          External scientific communications i.e. manuscripts, abstracts, response documents, etc.

o          Protocol and results summaries to support clinical trial disclosure commitments

•           Systematically perform quality control checks of documents prepared by colleagues against pre-specified check-list generated in the   
             project or SOP

•           Perform detailed analyses on a planned and ad hoc basis, relating to processes and their outputs

•           Ensure to abide with Client process

Job Requirements

•           Educational qualifications: Any graduate degree in life sciences.

•           Required Experience -  2 to 3 years

•           Good knowledge of basic computer applications, e.g. MS Word/ PowerPoint/ Excel, will be required

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