Medical Writer

Job Description

Designation: Medical Writer

Status: Full-time

Hybrid mode

ctc- 6lpa

sat sun fixed off

Shift timing - 9:30 to 6:30

Telephonic interview

Location - Prabhadevi

Job Description:

 Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area

 Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract,

Review articles and Medico-marketing inputs)

 Should be able to develop LBL, Poster, News-letters, KOL cases, booklets, atlas, guideline booklet, product

monographs, calendars, compendium, customized journals, handbooks, conference abstract booklets,

yearbooks, KOL opinion booklets, case studies, CMES, etc.

 Should have hands on experience in literature search and systematic review

 Should be accountable for medical writing deliverable and should ensure work on assigned projects adheres

to industry/international standards

 Should be able to draft article on Health Economic Outcome Research and understanding on subject will be

added advantage

 Should be responsible for continual improvement of in-house medical writing capabilities

 Should have an excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication

practices and standards.

 Should liaise with internal team, clients, authors and KOLs

Experience: Min 3 - 5 years’ experience

Qualification:

 Bachelor’s degree / Master’s Degree in any Pharma / Lifesciences/ Science related field.

 Excellent verbal and written skills (English).

 Good organizational, interpersonal, and team skills.

 Ability to deliver results under pressure.

 Goal oriented, self-motivated; able to work independently but within a team environment

Desired Skills/Experience:

 A good understanding of the healthcare market, challenges, growth prospects and healthcare delivery

operations

 Strong customer and contact network in healthcare domain

 A minimum of three – five years medical writing experience within the pharmaceutical industry or a contract

research organisation.

 Able to work independently, initiate their own projects as needed to streamline their workload, understand the

business process and work in a team environment

 Capacity to manage multiple projects with tight deadlines; working after hours to meet project deadlines if

needed

 Comprehensive understanding of English grammar and punctuation.

 Should be extremely detail oriented

 Ability to manage and prioritize several tasks and requests simultaneously