Pharmacovigilance, Team Manager
hace 1 mes
We are looking for Team Manager Pharmacovigilance to join our team in Barcelona on a permanent basis.
All over the world, decision-makers depend on us for the essential knowledge that can justify their strategies, promote outstanding research and business growth, and keep them abreast of the market.
You’ll join our Life Sciences Pharmacovigilance 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
- Degree in Life Sciences (Toxicology, Pharmacology, Biology, Pharmacy, Biomedical Sciences, etc.) and experience in pharmacovigilance, drug safety management and/or toxicology
- At least 5 years’ experience in a global corporation (pharma domain or consulting) with people and process management experience
- Excellent written and oral communication skills in English.
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?
- Create a culture of success, motivating, and developing colleagues to achieve their full potential.
- Drive execution and performance. Ensure key performance indicators for quality, timeliness and completeness are delivered and strive for continuous improvement.
- Build a customer-focused team and develop an environment which stimulates innovation.
- Play a role in major decisions and initiatives to enable the Content Function to achieve its long-term objectives.
- Communicate initiatives to senior management, set timelines and manage expectations for all deliverables and releases.
- Work together with Product, Product Operations, Technology and Marketing in the product development process
- Identify opportunities for synergies and simplification of complex processes.
About the Team
- You’ll be reporting to the Director, Content Editing, Regulatory and Market Access based in France and join an international and diverse team of more than 80 colleagues mostly based in Spain and India
- Your team is composed of around 20 colleagues mostly based in Spain and India
- 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 role 40 hours per week in Barcelona, EU hours. Hybrid, going to our central office 2-3 times per week.
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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