Senior STEM Content Specialist (Drug Safety Expert)
Senior STEM Content Specialist (Drug Safety Expert)
Apply remote type Hybrid locations Spain - Barcelona time type Full time posted on Posted Yesterday job requisition id JREQ131821
We are looking for a Senior Drug Safety, Content Specialist to join our team in Barcelona.
You'll join our Life Sciences OFF-X team, responsible for the curation of drug safety information collected from journals, congress publications and drug regulatory approvals which are delivered to OFF-X, a translational drug safety intelligence portal that allows users to easily identify new drug and target safety liabilities.
About You – experience, education, skills, and accomplishments
* Bachelor's degree in Life Science (Toxicology, Pharmacology, Biology, Pharmacy, Biomedical Sciences, etc.) and experience in drug safety management and/or toxicology
* At least 5 years' experience in a global corporation (pharma domain or consulting)
* Deep knowledge in drug safety management and/or toxicology
* + 2 years of experience working in a global, matrix, and virtual environment with cross-cultural clients or teams.
* Excellent project management capabilities with a strong focus in identifying opportunities for synergies, content enhancements and simplification of complex processes.
* Excellent oral and written English communications.
It would be great if you also had
* Demonstrated ability to work collaboratively in a matrixed organization.
* Good judgment in decision-making and priority setting.
* 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.
What will you be doing in this role?
* Design strategies to deliver high quality and timely content. Resolve complex data curation.
* Act as primary escalation point for resolving content customer queries using high scientific or technical expertise.
* Build partnership and work collaboratively to deliver complex scientific or technical content projects.
* Research and analyze content on new science or technology trending topics and identify training. Mentor the team.
* Identify system inefficiencies and/or error states and create stories for remediation development.
* Analyze and identify technology training and developmental needs for yourself or team on an ongoing basis.
* Maintain a flexible and adaptable approach towards process change.
* Implement plans based on guidelines that know the most efficient process for getting things done, with a focus on continuous improvement.
* Communicate effectively plans to drive results and ensure accountability.
* Develop and maintain relationships with product content and development stakeholders.
About the Team
* You'll be reporting to our Director, Regulatory and Safety Content Analysis, based in France.
* The team culture is dynamic, creative, and supportive – excellence, integrity, and care are in our DNA.
* You'll have 40 annual paid hours of volunteering time and the chance of being part of an active volunteering community which promotes diversity and inclusion across the business.
Hours of Work
This is a permanent full-time position at 40 hours a week (35 hours during July and August). The position is hybrid going to our office in Barcelona (next to Sagrada Familia) 2-3 times per week.
What we can offer
* Active volunteering community, with 40 annual paid hours of volunteering time.
* Private Health and Life & Disability insurances.
* Tax-free benefits (Ticket Restaurant scheme, kindergarten and transport cards).
* Language classes (Catalan, Spanish and English).
* Global and dynamic employee base (more than 20 nationalities).
* 30 working days holidays.
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.
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