SENIOR CONTENT SPECIALIST (BIOMEDICINE)

We are looking for a Senior Content Specialist to join our Biomedicine team in Barcelona.

If you hold a PhD in Life Sciences and have a deep understanding of the scientific literature, patents, clinical trials, FDA documents etc we are looking for you. You’ll be using your scientific expertise to ensure that the information is properly presented and organized following Editorial policies in Cortellis Drug Discovery Intelligence.

Our bold mission is to help customers solve some of the world’s most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of science and intellectual property.

If you are excited about the opportunity to work with our vibrant Life Sciences & Healthcare (LS&H) group, we would like to hear from you.

About You – experience, education, skills, and accomplishments  

• PhD in Life Sciences (Biomedical Sciences, Biotechnology, Biology, etc.).
• 5 years’ experience in a global corporate setting and with a strong knowledge of LS & H content.

It would be great if you also had the following:

• Involved in solving internal/external queries.
• Ability to analyze processes, identify problems, and develop effective solutions.
• Capability to work remotely with peers in an international environment.
• Ability to delve deep into content and results
• Knowledgeable in SQL query language
• Demonstrated ability to work collaboratively in a matrixed organization.
• Good judgment in decision-making and priority setting.             

​​What will you be doing in this role? 

• Deep understanding of the scientific literature, patents, clinical trials, FDA documents etc., and should be able to take the ownership of Biomedicine policies.
• Uses scientific expertise to ensure that the information is properly presented and organized following Editorial policies in Cortellis Drug Discovery Intelligence.
• To address and resolve internal and external queries effectively.
• Work together with Product Operations, and Technology in the development process/product.
• Participate in the quality control process to ensure accuracy and compliance with standards.
• Initiate/support projects that can enhance content and processes.
• Develop and deliver training sessions for internal team on new policies/enhancements.

About the Team  

• You’ll be reporting to the Team Manager, Content Editing, Biomedicine and join an international and diverse team of around 15 colleagues mostly based in Spain and India.
• The team culture is dynamic, creative, and supportive – excellence, integrity, and care are in our DNA.

Hours of Work

This is a permanent full-time position (40 hours per week), Hybrid going to our Barcelona central office (next to Sagrada Familia) 2-3 times per week.

Benefits:

• A start up culture/working environment combined with all the financial and stability advantages of working for a publicly traded company.
• 30 working days of vacation
• Volunteering community, with 40 paid hours of volunteering time
• Private Health and Life & Disability insurances.
• Tax-free benefits (Ticket Restaurant scheme, kindergarten, and transport cards)
• Agile work environment with a team of talented colleagues
• On-site language classes (Catalan, Spanish and English)

At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.