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Senior STEM Content Specialist (Clinical Expert)

Clarivate
Full-time
On-site
Barcelona, Catalonia, Spain
🌐 Digital Marketing

πŸ“Œ Core Information

πŸ”Ή Job Title: Senior STEM Content Specialist (Clinical Expert)

πŸ”Ή Company: Clarivate

πŸ”Ή Location: Barcelona, Spain

πŸ”Ή Job Type: Full-Time, Hybrid

πŸ”Ή Category: Life Sciences

πŸ”Ή Date Posted: April 4, 2025

πŸ”Ή Experience Level: Mid-Senior Level

πŸ”Ή Remote Status: On-site with hybrid options

πŸš€ Job Overview

Key aspects of this role include:

  • Curating high-quality clinical content from various sources for Clarivate's products
  • Designing strategies to deliver content timely and efficiently
  • Acting as the primary escalation point for content queries using scientific expertise
  • Collaborating with cross-functional teams in a matrixed environment
  • Identifying content enhancement opportunities and driving continuous improvement

ASSUMPTION: This role requires a strong scientific background and excellent project management skills to succeed in a dynamic, international team.

πŸ“‹ Key Responsibilities

βœ… Curating and updating clinical information from various sources such as clinical trial registries, press releases, scientific journals, congress abstracts, company websites, and FDA documents

βœ… Designing and implementing strategies to deliver high-quality and timely clinical content

βœ… Resolving complex data curation issues and acting as the primary escalation point for content queries

βœ… Building partnerships and working collaboratively with internal and external stakeholders to deliver complex clinical content projects

βœ… Researching and analyzing content on new scientific trending topics to identify Clinical content and product enhancement opportunities

βœ… Analyzing and identifying training and developmental needs for the team and implementing plans for remediation

βœ… Identifying system inefficiencies and error states and creating plans/initiatives for remediation

βœ… Communicating effectively to drive results and ensure accountability

βœ… Developing and maintaining relationships with Product and Technology stakeholders

ASSUMPTION: This role involves a high level of scientific expertise and requires strong problem-solving skills to manage complex data curation and content enhancement projects.

🎯 Required Qualifications

Education: PhD in Life Sciences

Experience: At least 5 years of experience in a global corporation analyzing and updating clinical information

Required Skills:

  • In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases
  • Excellent project management capabilities with a strong focus on identifying opportunities for synergies, content enhancements, and simplification of complex processes
  • Problem-solving skills and ability to deal with ambiguity and make decisions in a timely manner
  • Ability to work remotely with peers in an international environment

Preferred Skills:

  • Post-doctoral research experience
  • Customer-facing experience
  • Knowledge of Cortellis Trials Intelligence and Cortellis Drug Discovery Intelligence products
  • Ability to solve problems, focus on what's important, eliminate blockers, and define priorities properly

ASSUMPTION: Candidates with a strong scientific background and relevant experience in clinical information analysis will be most successful in this role.

πŸ’° Compensation & Benefits

Salary Range: €55,000 - €70,000 per year (Estimated, based on market research for similar roles in Barcelona)

Benefits:

  • Private Health Insurance
  • Life & Disability Insurance
  • Tax-free Benefits (Ticket Restaurant scheme, kindergarten, and transport cards)
  • Language Classes (Catalan, Spanish, and English)
  • 40 annual paid hours of volunteering time
  • 30 working days of vacation

Working Hours: 40 hours per week (35 hours during July and August), with a hybrid work arrangement (2-3 days in the office per week)

ASSUMPTION: The salary range is estimated based on market research for similar roles in Barcelona, as the original job listing did not provide specific salary information.

πŸ“Œ Applicant Insights

πŸ” Company Context

Industry: Information Services, focusing on scientific and academic research, patent analytics, and regulatory standards

Company Size: 10,000+ employees, providing a large, diverse work environment

Founded: 2015 (as a spin-off from Thomson Reuters)

Company Description:

  • Clarivate is a leading global provider of transformative intelligence, offering enriched data, insights, and analytics, workflow solutions, and expert services in Academia & Government, Intellectual Property, and Life Sciences & Healthcare
  • The company helps customers discover, protect, and commercialize new ideas, improve scientific research outcomes, and access critical information
  • Clarivate operates in over 40 countries and has a global employee base of more than 20 nationalities

Company Specialties:

  • Scientific and academic research
  • Patent analytics and regulatory standards
  • Pharmaceutical and biotech intelligence
  • Trademark protection
  • Domain brand protection
  • Intellectual property management

Company Website: clarivate.com

ASSUMPTION: Clarivate's diverse range of products and services cater to various industries, requiring employees to have a broad skill set and adaptability to different work environments.

πŸ“Š Role Analysis

Career Level: Mid-Senior Level, with opportunities for growth and development within the team and the broader organization

Reporting Structure: Reports to the Manager, Clinical, based in India, and works with an international team of more than 40 colleagues

Work Arrangement: Hybrid, with 2-3 days in the office per week at the Barcelona location

Growth Opportunities:

  • Expanding clinical content expertise and taking on more complex projects
  • Developing leadership skills and mentoring junior team members
  • Exploring opportunities within Clarivate's broader portfolio of products and services

ASSUMPTION: This role offers opportunities for professional growth and development within a dynamic, international team.

🌍 Location & Work Environment

Office Type: Hybrid, with an office located next to Sagrada Familia in Barcelona

Office Location(s): Barcelona, Spain

Geographic Context:

  • Barcelona is the second-largest city in Spain, known for its vibrant culture, architecture, and Mediterranean climate
  • The office is located in a central and easily accessible area of the city
  • Barcelona offers a high quality of life, with a rich cultural scene, diverse culinary options, and numerous outdoor activities

Work Schedule: 40 hours per week (35 hours during July and August), with flexible working hours and remote work options

ASSUMPTION: The hybrid work arrangement and central office location provide a good balance between work-life integration and collaboration with team members.

πŸ’Ό Interview & Application Insights

Typical Process:

  • Online application submission
  • Phone or video screening with the hiring manager
  • Technical assessment or case study presentation
  • Final interview with the hiring manager and/or other team members

Key Assessment Areas:

  • Scientific knowledge and expertise in clinical trials and drug development
  • Project management skills and ability to handle complex data curation
  • Problem-solving skills and adaptability to ambiguity
  • Communication and collaboration skills, both written and verbal

Application Tips:

  • Highlight relevant scientific and project management experience in your resume
  • Tailor your cover letter to demonstrate your understanding of the role and your fit with Clarivate's company culture
  • Prepare for the interview by researching Clarivate's products and services and thinking about how your skills and experience align with the role's requirements

ATS Keywords: Clinical trials, drug development, project management, data curation, scientific expertise, content enhancement, continuous improvement

ASSUMPTION: Clarivate's application process is designed to assess candidates' scientific expertise, problem-solving skills, and cultural fit within the organization.

πŸ› οΈ Tools & Technologies

  • Cortellis Drug Discovery Intelligence
  • Cortellis Trials Intelligence
  • Clinical trial registries (e.g., ClinicalTrials.gov, EU Clinical Trials Register)
  • Scientific literature databases (e.g., PubMed, Embase)
  • Project management tools (e.g., Asana, Trello)
  • Collaboration tools (e.g., Microsoft Teams, Slack)

ASSUMPTION: The tools and technologies required for this role are primarily focused on clinical content curation and project management, with an emphasis on scientific expertise and collaboration.

πŸ‘” Cultural Fit Considerations

Company Values:

  • Think Forward
  • Act with Integrity
  • Collaborate with Respect
  • Deliver with Excellence

Work Style:

  • Dynamic and creative
  • Supportive and inclusive
  • Focused on excellence, integrity, and care

Self-Assessment Questions:

  • How do you stay up-to-date with the latest developments in clinical trials and drug development?
  • Can you provide an example of a time when you had to manage a complex data curation project, and how did you approach it?
  • How do you balance the need for continuous improvement with the need to deliver high-quality content on time?

ASSUMPTION: Clarivate values employees who are forward-thinking, act with integrity, collaborate effectively, and deliver high-quality work. Candidates who can demonstrate these values and work styles will be a good fit for the organization.

⚠️ Potential Challenges

  • Managing complex data curation and content enhancement projects with tight deadlines
  • Adapting to a dynamic, international work environment with remote team members
  • Balancing the need for continuous improvement with the need to deliver high-quality content on time
  • Navigating a large, matrixed organization with multiple stakeholders

ASSUMPTION: These challenges can be overcome by strong project management skills, adaptability, and effective communication and collaboration with team members and stakeholders.

πŸ“ˆ Similar Roles Comparison

  • Unlike other content specialist roles, this position requires a strong scientific background and expertise in clinical trials and drug development
  • This role focuses on curating clinical content for Clarivate's products, while related roles may have a broader focus on scientific or academic research
  • Career progression in this role may involve expanding clinical content expertise, taking on more complex projects, or exploring opportunities within Clarivate's broader portfolio of products and services

ASSUMPTION: This role offers unique opportunities for candidates with a strong scientific background and a passion for clinical content curation and enhancement.

πŸ“ Sample Projects

  • Developing and implementing a new strategy for curating clinical trial data from various sources, improving efficiency and accuracy
  • Identifying and analyzing new scientific trending topics to inform content enhancement opportunities for Clarivate's products
  • Collaborating with cross-functional teams to deliver a complex clinical content project, managing stakeholders and ensuring high-quality output

ASSUMPTION: These sample projects demonstrate the range of responsibilities and opportunities available in this role, from strategic planning and analysis to cross-functional collaboration and project management.

❓ Key Questions to Ask During Interview

  • Can you describe the team structure and how this role fits within the broader organization?
  • What are the most challenging aspects of this role, and how have previous incumbents succeeded in overcoming them?
  • How does Clarivate support the professional development and growth of its employees in this role?
  • What are the key priorities for this role in the first 30, 60, and 90 days?
  • How does Clarivate foster a culture of collaboration and innovation in its teams?

ASSUMPTION: These questions are designed to help candidates better understand the role, the team, and the organization, enabling them to make an informed decision about their fit with the position and Clarivate's company culture.

πŸ“Œ Next Steps for Applicants

To apply for this position:

  • Submit your application through the application link
  • Tailor your resume to highlight your relevant scientific and project management experience
  • Write a cover letter that demonstrates your understanding of the role and your fit with Clarivate's company culture
  • Prepare for the interview by researching Clarivate's products and services and thinking about how your skills and experience align with the role's requirements
  • Follow up with the hiring manager within one week of submitting your application to express your interest in the role

⚠️ This job description contains AI-assisted information. Details should be verified directly with the employer before making decisions.