Require Deputy Manager at Excelra

Excelra provides a wide range of data and analytical solutions helping Biopharma companies in medicinal and computational chemistry, target identification, drug discovery, drug repurposing, indication prioritization, biomarker identification, patient stratification, clinical outcomes modelling and meta-analysis, clinical trial design and go/no-go decision, health economics outcomes research and market access.

Post : Deputy Manager - Scientific Writer

Job Description
Role: Challenging work that is an amalgamation of an understanding of medical science and health economics and outcomes research (HEOR) for scientific writing and market access.

Roles and responsibilities:
• Ensure timely production of high-quality documents (value dossiers, manuscripts, literature reviews, review articles, etc.) for presentation in value assessment meetings or publication in journals and of other written communication material supporting pharmaceutical brands, research activities, and business needs
• Prepare documents that are HTA submission ready
• Work with international pharmaceutical clients and liaise with internal and external stakeholders
• Effectively and proactively communicate with team members, and clients
• Act as document specialist and provide intellectual input across document types
• Provide quality-related coaching or mentoring to team members, as appropriate
• Develop, maintain and use necessary templates, formats, and styles to ensure that documents generated meet industry, internal, and client requirements

Candidate Profile
• PhD/MD (Pharmacology) OR PhD (HEOR) OR MBBS/MPH with knowledge of clinical research, health economics and outcomes research and medical writing
• At least 3-4 years of experience of writing HEOR documents and clinical trial publications in a medical communications agency or in a scientific writing/HEOR team in a pharmaceutical Company
• Advanced knowledge of clinical research processes, and evidence generation methodologies, as well as ISPOR, CONSORT, and other such industry guidelines
• Proven skills in writing and editing documents for regulatory (HTA) submissions and publications, including interpretation and summarization of complex outcomes data across multiple studies and phases
• Knowledge of methods and techniques for analysis and presentation of statistical results
• Excellent literature reviewing capabilities
• Excellent data interpretation and presentation skills
• Clear, concise scientific style of writing with a high level of attention to detail
• Ability to work under tight timelines

Additional Information
Experience : 2 - 4 Years
Qualification : PhD/MD, PhD (HEOR) OR MBBS/MPH
Location : India
Industry Type : Pharma
Functional Area : Scientific Writer
End Date : 15th July, 2018