Vacancy for post of Quality Reviewer, Regulatory Writing at Cactus

CACTUS is a pioneering global scientific communications company. In everything we do, we want to accelerate the development of global scientific research, by helping science break through the confines of geography and language. To this end, we partner with academic and pharmaceutical communities worldwide and leverage the expertise of 1400+ professionals to create compelling, high-quality scientific communications. Browse through the tabs below for a closer look at CACTUS.

Post:Quality Reviewer, Regulatory Writing

Job description
The medical writing team at CACTUS works with multinational pharmaceutical companies, clinical research organizations, and researchers worldwide to help them communicate their science. We are currently looking to add to our team, an experienced regulatory writer who wishes to be part of a world-class delivery team, and work in an exciting, fast-paced global environment

As part of his/her key responsibilities, the Quality Reviewer at CACTUS will

Review regulatory documents (e.g., protocols, amendments, IBs, CSRs, eCTD, summary documents, appendices, and clinical trial disclosures) for data accuracy against source data and consistency between the document text and the in-text tables
Review the content of the above-mentioned regulatory documents from a scientific and regulatory perspective
Check for grammar, syntax, style, and compliance with style guides, regulatory guidelines, and publishing requirements
Check documents generated by writers for data errors by checking annotated references
Check documents generated by writers for fact errors (discrepancy between source data and document, discrepancy within text, discrepancy between figures/tables and text)
Be responsible for the accuracy of data (numerical and otherwise) in the documents/projects assigned
Ensure timely delivery of documents

Candidate Profile
This position requires:

Minimum 3 years of experience in writing CSRs and/or other CTD sections either as part of a pharmaceutical regulatory writing team or in large, global CROs.
A university degree (MBBS/MD/MS or masters degree preferably in the pharmaceutical sciences) or equivalent industry experience
Ability to work efficiently and independently, multitask, and prioritize
Excellent attention to detail
Ability to concentrate and work under pressure and meet tight deadlines
Excellent written and oral communication skills
Functional with Microsoft Word, Excel, and PowerPoint
Flexible and adaptable to changing project priorities and work assignments

Additional Information
Experience: Min. 3 Years
Qualification: M.Pharm, M.Sc
Functional Area: QC
Location: Mumbai
Last Date: 18^th May, 2017