Indegene MANAGER SCIENTIFIC WRITING – PHARMACOVIGILANCE M.Pharm,B.Pharm,MBBS
About Indegene:
At Indegene, we look to change healthcare for the better.
Being an Indegene employee is not just doing a job, but it is about real
contribution and outcomes. We are a global team of over 1,200 employees across
14 global locations. Our singular focus is to deliver real outcomes that are
measurable, impactful, and sustainable. This has made us a recognized global
leader and partner to some of the largest and most respected healthcare
organizations.
Joining us means you will be part of a great company, one
that joins hands to really improve patient and business outcomes using
analytics, technology, operations, and medical expertise. Our people are
exceptionally bright, motivated, and customer focused. Even though they are
from diverse cultural and academic backgrounds, they have three things in
common—they are really passionate about healthcare, they are committed to their
customers and teams, and they sincerely believe that collaboration is the key
to achieving their personal and professional goals.
Job Summary:
The Manager Scientific Writing—Pharmacovigilance needs to
lead and manage delivery of projects in terms of resourcing, quality,
timeliness, efficiency, and high technical standards for deliveries made by the
medical writing group, including scientific documents and clinical/medical
reports. He or she contributes to overall quality enhancement by ensuring high
scientific standards for the output produced by the medical writing group
through expert review and feedback mechanism to the delivery teams.
Job Description:
The roles and responsibilities of the Manager Scientific
Writing—Pharmacovigilance include the following:
Developing
scientific medical content for all projects that meet international quality
standards
Interfacing
with clients on a regular basis to meet their expectations
Controlling/reducing the cost of content development, cycle times, and
error rates in projects
Developing
innovative medical content products by leveraging on the depth of scientific
content
Adhering to
compliance procedures and internal/operational risk controls in accordance with
any and all applicable regulatory standards, requirements, and policies
Desired Skills and Experience:
Education—MD/PhD/MBBS/M.Pharm
Experience—5-7 years of experience in pharmaceutical companies in any of
the following functions: medical services/medico-marketing/clinical research/regulatory
affairs; medical writing/developing/publishing medical content; or a minimum of
1-3 years of experience in any clinical practice
Understanding
of any specialty area of medicine (preferred) or an overall understanding of
the medical field
Strong flair
and passion for writing
Strong
written and verbal communication/presentation skills
Passion for
networking and updating oneself with the latest technical/scientific
developments and relating them to various projects
Strong
clinical reasoning skills
Ability to
work under pressure to meet agreed deadlines
Passion,
energy, and enthusiasm to drive results
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