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✨ WHY CHOOSE MEDSIR ✨ We are a Barcelona-based fastest-growing company founded by scientific experts 🔬. We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of...
✨ WHY CHOOSE MEDSIR ✨

We are a Barcelona-based fastest-growing company founded by scientific experts 🔬. We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results 💊📃. Together, we create the best strategies that are both clinically relevant and scientifically meaningful 💉. We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way 🚀.

At MEDSIR, you will have the job of your life while working together towards our shared 🌟 mission 🌟 bringing novel treatments to cancer patients worldwide. We welcome top performers that will bring new ideas, diverse perspectives, and provide you the opportunities and freedom to grow and make a real impact ❤ in patients' lives and science… all while having great fun 🎉

🤓 ABOUT THE OPPORTUNITY:

The Clinical Research Development and Communication Specialist is a hybrid role that bridges MEDSIR’s two Scientific teams, integrating complementary responsibilities. This position is responsible for facilitating the conception and design of new research projects, as well as supporting their execution of research projects by delivering key documents essential to the conduct of clinical studies. Additionally, the role involves generating publications and other scientific materials to raise awareness of MEDSIR’s research initiatives.

🎯 HOW YOU WILL CONTRIBUTE:

Scientific Deliverables

  • Generate and/or review scientific documents required for MEDSIR projects, including but not limited to clinical trial synopses, study protocols, clinical study reports, molecular reports, and other trial-specific documents that demand specialized scientific and medical knowledge.
  • Generate and/or review scientific publications resulting from MEDSIR activities, including abstracts, posters, presentations, and manuscripts.
  • Develop and/or review medical and scientific materials intended to raise awareness of MEDSIR's research among various stakeholders such as patients, healthcare professionals, and the biopharma industry.
  • Direct involvement in document preparation or supervision of outsourced activities as needed.


Project Design

  • Contribute actively to the brainstorming and development of new clinical research project designs.
  • Identify and provide key scientific and clinical assumptions that influence project planning and budgeting.


Stakeholder Engagement

  • Provide ad hoc support during proposal defenses with external clients (e.g., pharmaceutical companies) and collaborators (e.g., renowned oncologists).
  • Liaise directly with clients and authors/speakers on various scientific and medical projects.


Regulatory Compliance

  • Ensure all deliverables comply with applicable regulations, standards, and guidelines, including ICH, GxP, internal company policies, journal requirements, and international writing standards.
  • Set up clinical trial in public registries such as ClinicalTrials.gov, EUCTR, or equivalent databases.


Organizational Management

  • Monitor deadlines and ensure timely delivery of all scientific and medical outputs.
  • Maintain organized records, inventories, or platforms related to MEDSIR’s medical and scientific deliverables.
  • Participate in departmental administrative tasks and responsibilities.
  • Contribute to the development and continuous improvement of departmental and company-wide procedures.


Scientific Awareness

  • Stay up to date with current medical literature, emerging science, technological advancements, and medical trends.


💪WHAT DO WE VALUE FOR THIS OPPORTUNITY?

  • Robust scientific background: Advanced degree (Ph.D., M.D., Pharm.D., or equivalent) in a scientific or medical discipline related to clinical research.
  • Strong understanding of clinical trial methodology, regulatory requirements, and industry standards (e.g., GCP, ICH guidelines).
  • Excellent communication skills, with the ability to effectively communicate scientific concepts and findings to diverse audiences.
  • Proven ability to work collaboratively in a cross-functional team environment and effectively manage multiple priorities in a fast-paced setting.
  • Strong analytical and problem-solving skills, with a detail-oriented approach to scientific review and data interpretation.
  • Proficiency in scientific writing and publication development, including experience with scientific presentations.
  • Ability to work independently and with minimal supervision.  
  • Good computer skills, proficient with Microsoft office applications.  
  • Fluency in English.
  • Proficiently work on Apple devices/MacBook. 


📢 THE THINGS YOU REALLY WANNA KNOW 😉:

At MEDSIR, we believe that employees today want to evolve in collaborative, high-growth environments where they can demonstrate their abilities and thrive both professionally and personally. We are convinced that employees need to find alignment between their inner values and their company’s culture and mission to unlock their full potential. We work to create a culture of empowerment, continuous learning and growth where everyone can bring expertise, own projects and easily measure their impact 🙌

Benefits

🤓 Work with world-renowned clinicians and KOL´s on high-level publications and papers.

🚀 Fast growth, we are an early-stage company with a multidisciplinary team and many growth opportunities.

🏡 Work-life balance - hybrid working model and flexible hours focusing on performance rather than office hours.

🎓 Unlimited access to GoodHabitz courses and regular workshops (external & internal) to continue your development.

📚 Opportunities to participate in scientific conferences & events at national and international level.

💉 Private health Insurance.

🏝 Work-from-abroad policy depending on position and local legislation.

🌏 A young & international team with a company culture focused on development.

☕ Positive, dynamic, and passionate work environment.

💪🏽 Elevate your wellness with Wellhub (formerly GymPass)! One subscription for the best in fitness, mindfulness, therapy, nutrition, and sleep support—all in one place.

💸 "Flexible compensation plan" to help you save taxes and increase your net salary (Cobee).

🎂 A free day on your birthday so you can truly celebrate!

🎉 Unforgettable MEDSIR events and regular get togethers.

👥 Equal employment opportunity, at MEDSIR we proudly pursue a diverse workforce and celebrate our differences.

🌇 A fantastic workplace located in 22@, Barcelona's new hub of innovation.

💻 We work with MacBook computer (Apple).

If you believe you match our values, you are unique and feel ready to make a change, we look forward to meeting you!

🧡 We are committed to fostering a diverse and inclusive workplace, where all individuals are treated with respect and equality, regardless of race, gender, age, religion, disability, or any other characteristic. We believe in providing equal opportunities for all and do not tolerate discrimination in any form.

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