Editor - Competitive Intelligence, Drug Identification
Clarivate
Barcelona, Spain
hace 31 días

Clarivate Analytics clients are the trailblazers and risk takers who come up with life-changing ideas. We’re looking for our own trailblazers to help us keep providing clients some of the world’s most trusted brands, spanning scientific and academic research, patent analytics, pharmaceutical and biotech intelligence and IP management.

We’re an independent owned company with a rich heritage and a bold entrepreneurial mission. If you’re excited by the thought of helping people and organizations go from new ideas to life-

changing innovations faster, we’re excited to consider you for a position at Clarivate.

Editor (Advanced therapies) Competitive Intelligence, drug identification

Clarivate Analytics accelerates the pace of innovation by providing trusted insights and analytics to customers around the world, enabling them to discover, protect and commercialize new ideas faster.

We own and operate a collection of leading subscription-based services focused on scientific and academic research, patent analytics and regulatory standards, pharmaceutical and biotech intelligence, trademark protection, domain brand protection and intellectual property management.

Clarivate Analytics is now an independent company with over 4,000 employees, operating in more than 100 countries and owns well known brands that include Web of Science, Cortellis, Derwent, CompuMark, MarkMonitor and Techstreet, among others.

For more information, visit clarivate.com.

Within the Life sciences group, the Business of Science team is responsible for Cortellis content (Competitive Intelligence, Clinical trials Intelligence & Regulatory Intelligence).

The editor role within the Cortellis Competitive Intelligence (CCI) will contribute to maintenance and development of CCI drug related content.

Main purpose of the job

The drug team is a globally-located editorial team specifically responsible for data relating to commercial, proprietary drug development activity, which is collected in the form of individual drug records.

The team analyses scientific and industry source data to provide value-add content for the competitive intelligence community in the pharmaceutical industry and beyond, with a strong emphasis on accuracy, timeliness and comprehensiveness.

As an Editor, your responsibility is identification, analysis and processing of pharmaceutical information from any relevant source which could include pharmaceutical company websites, regulatory agencies, investor presentations, press releases or scientific conferences.

Specializing in advanced therapies (cell therapies or gene therapy) , and with a background in molecular biology, you will also have additional responsibility for helping to manage the consistency, accuracy and comprehensiveness of content related to pipeline cancer drugs, which form a significant proportion of the Clarivate databases.

The team you will be part of also plays an important role in managing ongoing content and policy development, in conjunction with relevant editorial, strategy and development teams, so you would be expected to quickly acquire a strong functional knowledge of relevant policies and their impact on the customer in order to support this, and apply this to advanced therapy area in particular.

The role also includes attendance at national or international biomedical conferences, from which attending editors report and collect relevant data.

Finally, the role may also offer the opportunity to contribute to cross-functional process and automation projects designed to improve the efficiency of editorial operations.

Main duties

1. Ensure the daily provision of drug information for Cortellis contents according to relevant quality, timeliness and completeness targets

2. Ensuring the consistency and accuracy of cancer-related content in drug and other datasets

3. Support the development, maintenance and communication of editorial policies relevant to the above content

4. Work with other departments as required to deliver on targets or business requirements

5. Contribute to cross-functional process and automation projects to improve the efficiency of editorial operations

6. Report and update from any attended conferences

7. Undertake any other reasonable duties as requested by the line manager

Skills and experience

  • Educated to PhD level in molecular biology or similar, with specialization in cell therapies (preferred specialization) oncology or immunology.
  • First experience in pharmaceutical industry or clinical research organization
  • Excellent organizational capabilities
  • Good interpersonal skills
  • Strong problem identification and solving skills
  • Excellent communication skills, both written and verbal
  • Ability to work both independently and collaboratively
  • Good team spirit
  • Ability to travel (10 to 20 % of time to attend conferences worldwide).
  • It is the policy of Clarivate to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, pregnancy, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.

    In addition, Clarivate will provide reasonable accommodations for qualified individuals with disabilities.

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