Associate Content Editor – Clinical Studies Jobs for BPharm, MPharm, Biotechnology, Microbiology
- Introduction: Paving the Way for Medical Advancements
- The Role: A Closer Look
- Key Responsibilities
- Qualifications and Expertise
- Joining the Clinical Studies Team: A Remarkable Opportunity
- About the Team
Are you fascinated by the world of clinical research, pharmaceuticals, and drug development? Do you possess strong analytical skills and a passion for detail? If so, the role of an Associate Content Editor in the Clinical Studies team might be the perfect fit for you. In this article, we will delve into the exciting responsibilities, qualifications, and opportunities this position offers, shedding light on the critical role it plays in advancing medical knowledge and patient care.
Introduction: Paving the Way for Medical Advancements
In the realm of clinical studies, the role of an Associate Content Editor is akin to that of a meticulous detective. These professionals are entrusted with the responsibility of actively seeking out, analyzing, and updating information related to clinical studies from a diverse range of sources. By cross-referencing data from scientific meetings, conferences, trial registries, press releases, and other internet sources, they contribute significantly to maintaining accurate and up-to-date clinical records.
The Role: A Closer Look
Key Responsibilities
As an Associate Content Editor, you will be on the frontlines of clinical information management. Your primary duties will include:
- Maintaining the Clarivate database with accurate and current clinical trials information sourced from various outlets.
- Being accountable for meeting weekly targets, ensuring consistent and timely updates.
- Upholding stringent quality standards to guarantee the accuracy and reliability of the information presented.
- Demonstrating the ability to comprehend and interpret intricate data related to trials and pharmaceutical drugs from source materials.
- Leveraging your inquisitive and analytical mindset to identify and solve problems that may arise during the information analysis process.
Qualifications and Expertise
To excel in this role, the following qualifications and expertise are highly valuable:
- A degree in BPharm, MPharm, or MSc in Biotechnology, Microbiology, or a related field.
- A minimum of 1 to 3 years of experience in analyzing and updating clinical reports.
- In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
- Exceptional written and verbal communication skills in English.
- Desirable experience in secondary research related to clinical information.
Joining the Clinical Studies Team: A Remarkable Opportunity
About the Team
The Clinical Studies team operates within the context of Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence. This dedicated team consists of 20 members, including Principal Content Analysts, Senior Content Analysts, Content Analysts, and Associate Content Analysts. Under the guidance of Team Manager Sree Vidya G, this team collaborates to drive insights and advancements in clinical research.
