GSK M Pharma Scientific Writer Vacancy 2022 – Apply Online
GSK Hiring pharm candidates for Scientific Writer, Scientific Writer, job opening 2022. Pharma job opening 2022. Pharmacy job opening 2022. Scientific Writer, job opening 2022. Candidates with bachelor’s and master’s degree in pharma may apply for the job opening at GSK. Check out all the details
Job Title: Scientific Writer
Location: Bengaluru, India
Req Id: 333653
Knowledge/Education Required:
Minimum Level of Education Required -MSc or MPharm
Area of Specialization – Life Sciences
Why is it required? – This is the minimum post-graduate qualification required for this entry grade. The role will require a good understanding of complex regulatory writing processes including data interpretation & skills to communicate information to target audiences. The post-graduate qualification should reflect the experience of independently conducting scientific research, data interpretation and the ability to write for a scientific audience. A Ph.D. would warrant the next level entry grade.
Previous Experience Required:
Minimum Level of Job-Related Experience Required –
- Up to 2 years of writing experience in the pharmaceutical industry is a plus.
- Demonstrates knowledge of scientific methodology in the design, conduct, and description of clinical research.
- Demonstrates understanding of how to interpret, describe and document clinical data.
- Ability to understand the importance of the International Committee for Harmonization (ICH) / Good Clinical Practice (GCP).
- Possesses good working knowledge of statistical principles used in clinical research
- Shows good attention to detail
- Possesses necessary computer skills and general computer literacy.
- Excellent English language skills (verbal and written)
Why is this level of experience required? – This level of experience will provide expertise for assigned activities and facilitate working independently on some projects.
Knowledge & Application – The level of knowledge required will be applied to work on assignments (to some extent) independently, facilitating the delivery of the written assignments through proactive coordination of stakeholders to build content. The writer should be able to meet the quality standards of the global organization. The Medical Writer is responsible for the final deliverable and is expected to work in complex matrix organizations.
Problem Solving & Innovation :
- Actively participates in document planning and review meetings.
- Demonstrates understanding of how to interpret and describe clinical data
- Proactively raises and discusses concerns/ issues in an open and timely manner within the global Medical Writing Team
- Promotes high medical writing standards by pointing out obvious flaws and proposing alternatives.
Interaction:
- Participates in document planning and review meetings.
- Raises and discusses concerns/ issues in an open and timely manner within the global team at GSK Pharma
- Establishes a network of communication and builds these relationships with stakeholders to facilitate efficient execution of assignment
- Has the ability to interpret and describe clinical data and discuss it with team.
- Promotes high medical writing standards by pointing out obvious flaws and proposing alternatives.
- Multi-Cultural Requirements: The role requires interactions in multicultural settings and in diverse environments for discussion with peers, project team members and stakeholders. The role also may require interactions with co-workers who are in virtual remote teams.
Impact :
- The role will contribute to the delivery of clinical R&D project milestones and ensures consistently high quality by doing the following:
- Completes assignments under the guidance of a mentor (this may include sections or whole documents and following defined templates).
- Promotes high medical writing standards by pointing out obvious flaws
- Has the ability to interpret, describe and document clinical data and discuss with team
- May attend planning, coordination, and review meetings.
Job Purpose of the Scientific Writer:
The Scientific Writer is expected to work under the guidance of a mentor or independently, facilitating the delivery of the written assignments through proactive coordination of stakeholders to build content. The writer understands trial designs and interpretation of statistically analyzed clinical research data. The writer should be able to meet the quality standards of the global organization. The Medical Writer is responsible for the final deliverable and is expected to work in complex matrix organizations.
Key Responsibilities:
- Completes assignments under the guidance of a mentor or independently (this may include sections or whole documents).
- Authors’ clinical regulatory documents following defined templates.
- Independently builds and expands capabilities to work on increasingly complex assignments.
- Understands the importance of consistency and quality level for all documents.
- Establishes a network of communication and continuously builds these relationships with stakeholders to facilitate efficient execution of assignments.
- Participates in document planning and review meetings.
- Proactively raises and discusses concerns/ issues in an open and timely manner within the global Medical Writing Team
- Promotes high scientific and medical writing standards by pointing out obvious flaws and proposing alternatives.
- Interprets and communicates clinical data clearly and succinctly and at an appropriate level for the audience.
Apply Online
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