Download Trialtrove (Citeline) Analyst

Trialtrove (Citeline) Analyst
Oncology
Location- US, remote
Trialtrove is the world’s most comprehensive real-time source of pharmaceutical clinical
trials intelligence, gathering clinical trial information from over 30,000 clinical trial data
sources to provide a continually updated reference of clinical trials research in more than
150 countries. Covering over 180 diseases in eight major therapeutic areas, it is the only
real-time service offering such breadth and depth of clinical trial data, supported by
experienced pharma industry analysts to guarantee the highest possible pharma business
intelligence value.
Role Description
Citeline, part of the international Informa Group, has a new opportunity for a Pharmaceutical Industry
Analyst to join their market-leading team, in the Oncology therapeutic area. As part of the Trialtrove
Research Team, the Analyst reports directly to the Therapeutic Area Director or Associate Director
and is a member of the Citeline Editorial team. The Analyst is broadly responsible for supporting
daily editorial operations, ensuring the quality and integrity of the Trialtrove database, providing
unparalleled research support to clients and supporting analytics projects. These objectives are
achieved through a solid understanding of varied clinical trial intelligence sources, collecting key
clinical trial data, conducting additional research and devising basic database search strategies for
clients, and performing basic data analysis. This is an excellent opportunity for an experienced Research
Analyst who is looking to progress their career and join a best-in-class business intelligence brand.
Role Responsibilities
Content Production
 Support Therapeutic Area team and maintain up-to-date and accurate databases for all
Citeline products
 Review, update, and add trial records based on company pipelines, trial sponsor events, trial
registries, medical literature/conferences, SEC filings and other web-based information
sources
 Acquire basic understanding of Therapeutic Area, including diseases, drugs/targets
treatment algorithms, patient attributes and scope of coverage
 Acquire basic understanding of and competence in internal content management systems to
master database functionality and all processes related to record creation and maintenance
 Acquire basic knowledge and understanding of inter-product relationships with other
Citeline products, and ensure consistency between data sets
Oversee Editors
 Review Editor work on trial records, answer queries and provide feedback to help develop
skills to full competency
 Review and assess performance, productivity and accuracy trends of Editor teams and
individuals
Client Support
 Provide prompt and accurate research support to clients
 Conduct primary/secondary research, assist with database search strategies and perform
basic data analysis
 Apply knowledge of the regulatory process, pharmaceutical drug development and clinical
trials to provide highest quality data and support to clients
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Assist with production of content for internal and external client projects, such as Citeline
Analytics and thought leadership pieces, and create client-ready deliverables in Excel, Word,
PowerPoint and/or PDF formats
Develop basic knowledge and understanding of the Citeline client management tool
Team Support
 Actively participate in team calls
 Learn roles and responsibilities of team and overall organizational structure of Citeline
 Attend role-specific training workshops as requested
 Support team during absences
 Perform other miscellaneous duties as assigned
Role Requirements
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BA or BSc, preferably in a life science or equivalent experience
Work experience, preferably at a pharmaceutical company, CRO, consulting/ market
research firm, or clinical/academic research site. Internship experience will be considered.
Familiarity with drug development process and associated pharmaceutical markets
Impeccable attention to detail and accuracy
Strong internet research skills
Ability to use sound logic to edit, manipulate and analyse different types of data.
Good organizational, time management and priority setting skills, and the flexibility to multitask in a fast-paced environment
Ability to think critically, work independently and follow instructions
Ability to work collaboratively within a team both in the office and off site
Working knowledge of Microsoft Excel, Word and PowerPoint
Excellent written and verbal English skills
To apply for this opportunity, please send your resume and a cover letter and salary expectations
to [email protected], quoting TrialtroveOncology
About Citeline
Citeline is the world’s most comprehensive source of real-time R&D intelligence for the pharmaceutical
industry, featuring an unmatched data collection of global clinical trials, clinical trial investigator profiles and
drug development pipelines.
About Informa
Informa is one of the world’s leading knowledge providers. The Business Intelligence division includes units in
the following industry verticals: Finance; Pharma & Healthcare; Telecom, Media & Technology; Maritime &
Law; and Agra.
Our passion for people extends from our employees to the global community. As a people company, we invest
in philanthropic causes, whether it be cancer research or disaster relief. In the office, we encourage a fun and
productive atmosphere
Informa is committed to equal employment opportunity for all employees and applicants for
employment without regard to age, color, creed, disability status, gender, national origin, race,
religion, sexual orientation or veteran status, or any other legally protected status.