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Cliantha Research Hiring Medical Writer / Scientific Writer - M.Pharm Apply

 

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Cliantha Research Hiring Medical Writer / Scientific Writer

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.

Post : Medical Writer / Scientific Writer – Consumer Research

Department : Consumer Research

Basic qualification required : M.Pharm

Experience : 2 - 6 Years

Location : Ahmedabad


Job Description
Area of Writing : Consumer Research, Nutraceuticals, Herbal, Cosmetics, Cosmeceuticals, Food and Functional Food, OTC products, Surface care products, Baby and Mother care products, etc.
Regulatory Knowledge : AYUSH, ICMR, COLIPA, FSSAI, ASCI, FDA, Health Canada, Japan, ASEAN guidelines - for Nutraceuticals |Traditional Medicines | Ayurvedic, Cosmetics and Personal Care Products General

Skills :
• A strong communicator with meticulous attention to detail,
• Has solid writing and organizational skills.
• Should be curious and motivated, and work well independently or as part of a team in high- pressure situations. In addition to these general skills and personality traits, we are seeking Medical Writer candidates with the following skills.
• Extensive knowledge of English grammar with a familiarity with a standard style guide and writing guidelines regulations
• Ability to communicate scientific or medical information in a clear and concise manner
• Proficiency in Word, Excel, PowerPoint, email, and the Internet
• Familiarity with the principles of clinical research
• Ability to interpret and present clinical data and other complex information
• Experience in a Medical specialty (i.e. Pharmacology, Biotechnology, Pharmaceutics, Pharmacognosy etc.)
• Thorough understanding of Indian, COLIPA, FSSAI, AYUSH, FDA and ICH regulations and guidelines
• Available writing samples
• Ensuring that the content, format and structure of their documents comply with regulatory, journal, or other guidelines
• Reviewing and proofreading materials to check quality and scientific accuracy
• Monitoring deadlines and ensuring projects are delivered on time so they can dovetail with other company-wide projects
• Liaising directly with clients and doctors/internal stakeholders on various projects
• Helping junior writers in their account team to develop so they reach their full potential

Most importantly, maintain a positive attitude toward all subjects/patients and fellow co-workers. The duties listed may be changed or modified at any time per project’s need.


Interested candidates can send their resume at apurohit@cliantha.com

Last Date : 30th June, 2023

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