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


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

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 birecruitment@informa.com
, 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.