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
As a CLINICAL TRIAL SCIENTIFIC WRITER you will develop/revise the design of clinical trial proposals and protocols, and contribute with the scientific estimates to the high-level execution plan for the new projects. As a Scientific Writer Specialist, you will be involved in projects under development and until they are ready for execution in hospitals worldwide, contributing both in the scientific and clinical development and in the medical writing of it.
The position reports to the Clinical Trial scientific writer Lead.
HOW YOU WILL CONTRIBUTE:
- Responsible for generating and/or reviewing scientific documents required as part of design of new MEDSIR clinical trials or updates on existing projects. Documents might include but are not limited to synopsis of new clinical trials, protocols, informed consent forms and other trial-specific documents that require a specialized scientific and medical knowledge. Responsibility might result in direct involvement in the preparation of those documents or supervision of outsourced activities.
- Responsible for identifying and providing the key scientific and clinical assumptions that impact on the project plan and budget.
- Ensure that all deliverables are in accordance with applicable regulations, standards, and guidelines, such as ICH, GxPs, Scientific and Company guidelines.
- Responsible for setting up new clinical trials in public registry databases (clinicaltrials.gov or equivalent databases).
- Monitoring deadlines and ensuring projects are delivered within agreed timelines.
- Staying current with Medical Literature and Advancements: must keep abreast of current literature, emerging science, technological developments, and medical trends.
- Supporting ad hoc in the defense of proposals with external clients (such as pharmaceutical companies) and collaborators (such as renown oncologists).
- Participating in the definition and improvement of department and company procedures.
- Participating in the administrative requirements of the department.
- Protect information from unauthorised use or access and notify the Information Security Officer and the Management System Officer in the event of such unauthorised access or use.
- Abide by the internal regulations, raise concerns and breaches related to compliance obligations, and collaborate with Ethics & Compliance as required.
Participate in scheduled company trainings.
WHAT DO WE VALUE FOR THIS OPPORTUNITY?
- Robust scientific background: at least MSc in health sciences and preferably PhD.
- Knowledge on the principles of clinical research.
- Solid writing and organizational skills with meticulous attention to detail.
- Proficiency in computer skills, including search databases, and MS office package or equivalent.
- Motivation and ability to keep scientific knowledge updated in areas required by the Company projects that include but are not limited to Oncology, Molecular biology, Digital innovation in Health Sciences.
- Ability to interpret and present clinical data and other complex information.
- Ability to communicate effectively in English and preferably in additional languages.
- Ability to communicate scientific or medical information in a clear and concise manner.
- Strong interpersonal, communication, facilitation, and presentation skills. Candidate must be able to work collaboratively with colleagues across all functions and at all levels.
- Strong analytical and problem-solving skills.
- Ability to work well independently and as part of a team in a deadline- driven environment.
- Flexible attitude in response to time demands and unexpected events.
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 (AXA).
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.
