Ofertes d'ocupació de Metge/essa a Barcelona

• Nivell d'experiència---
• Tipus de contracteConsultor
• Publicada18 de febr.

Teletreball

Proclinical is seeking a dedicated Freelance Medical Science Liaison with a focus on dermatology. This role involves supporting clinical development programs and building strong relationships with key opinion leaders and other stakeholders. The position is fully remote, based in Spain.

Responsibilities:

• Work alongside the clinical study teams to provide medical and scientific support for clinical sites.
• Develop and maintain relationships with clinical study investigators and key opinion leaders in dermatology.
• Serve as a credible scientific resource, offering up-to-date information on development programs.
• Stay informed about the latest developments and research in dermatology.
• Monitor competitor products and market trends.
• Work closely with cross-functional teams to ensure strategic alignment.
• Provide insights and feedback to internal teams from external interactions.
• Contribute to regional advisory boards.

Key Skills and Requirements:

• Advanced degree in a relevant medical or scientific field.
• Expertise in medical dermatology.
• Deep knowledge of clinical study execution.
• Past history with compliance requirements in medical affairs.
• Knowledge of dermatology therapeutic areas and treatment paradigms.
• Excellent communication and presentation skills.
• Ability to build and maintain professional relationships.
• Willingness to travel extensively, including attending scientific conferences.
• Willingness to travel up to 50% to clinical sites and attending medical/scientific conferences.

If you are having difficulty in applying or if you have any questions, please contact Tom Pinnock at [email protected]

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

• Flexibilitat horàriaSi
• Nivell d'experiència---
• Tipus de contracteConsultor
• Publicada18 de febr.

Python R MATLAB

Clinical Affairs Specialist (Medical Devices)Location: Barcelona, Spain

About Us: We are a pioneering start-up that creates lightweight, quick-to-adjust, and accessible robotic exoskeletons.

Our mission is to democratize access to this technology, improving the rehabilitation, health and quality of life of millions of people with mobility impairments.

We are seeking a passionate team member to work on our clinical research efforts, ensuring our products deliver measurable and meaningful benefits to patients.

Position Overview: As a Clinical Affairs Specialist, you will play a critical role in designing and managing clinical trials to gather evidence that demonstrates the efficacy of our robotic exoskeletons.

You will work closely with the Product, Clinical and Regulatory Affairs teams to ensure compliance, reliability, and scientific rigor of clinical activities at ABLE Human Motion.

Key Responsibilities: Clinical Trials: Design clinical trial protocols to evaluate the benefits of our robotic exoskeletons, cooperating with external partners (clinical investigators from hospitals).Clinical Evidence & Data Analysis: Analyze clinical trial data using statistical methods to draw meaningful insights.

Then, incorporate these analyses into the clinical evaluation documentation for the device (clinical evaluation report).Clinical Trial Site Management: Create and maintain any documentation associated with clinical trials, including protocols, case report forms, and investigator brochures.Site Monitoring: Communicate and work closely with clinical investigators to ensure adherence to protocols, regulatory requirements, and high-quality data collection.Scientific Communication: Collaborate with clinical investigators to prepare scientific manuscripts, posters and congress/conference presentations to share the findings.Literature Review: Design and conduct systematic literature searches to integrate the latest evidence in rehabilitation robotics into our clinical evaluation and protocols.Requirements: Degree in Life Sciences, Biomedical Engineering, Medicine, Physiotherapy or related.Previous clinical research experience, preferably within medical devices or rehabilitation.Excellent scientific writing and communication skills.Attention to detail and strong analytical abilities.Proficiency with statistical analysis (MATLAB, R or Python).Have a valid permit to work in the European Union.Proficiency in written and oral English.Preferred: Knowledge of medical device clinical evaluation regulatory requirements (Medical Devices Regulation, EU MDR) or previous experience in a regulated industry is highly desirable.Familiarity with Good Clinical Practices (GCP), ISO 14155 and ethical considerations.Flexible working hours, with the option of telework 2 days a week.Full-time contract of employment.How to Apply? Send an email to ****** attaching your CV with the subject "Clinical Affairs Specialist".

Seniority LevelEntry level

Employment TypeFull-time

Job FunctionHealth Care Provider

IndustriesMedical Equipment Manufacturing

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• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada17 de febr.

Teletreball Spark LESS

Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.

Responsibilities

• Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.
• Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.
• Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.
• Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.
• Establish and maintain effective team project service operations communications
• Liaise with Project Manager by proactively identifying issues and proposing solutions
• Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives
  
  

• Must be a Pharmacist.
• Excellent written and verbal skills in English (min. C1) and German language (min. C2 or native).
• Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.
• Excellent attention to detail and accuracy maintaining consistently high-quality standards.
• Excellent organizational skills and time management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.
  
  

• Bachelor’s Degree in Pharmacy
• Fluency in English (min. C1 level) and German language (min. C2 level or native).
  
  

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada10 de febr.

We offer:Unique opportunity to join the company in very exciting phase of business growthOpportunity to improve the quality of life for people worldwide by providing them simple and innovative solutions that improve their healthExtensive motivation programDynamic work environmentCareer development opportunities, professional as well as personal growthYour main responsibilities will be:Build and maintain strong relationships with key clients, serving as their primary point of contact for all business-related matters.Develop and implement strategic account plans to achieve sales targets, foster account growth, and identify new business opportunities.Conduct regular business reviews with clients to assess their needs, address concerns, and provide solutions that meet their objectives.Collaborate with cross-functional teams, such as sales, marketing, and customer support, to ensure seamless delivery of products/services and exceptional customer experience.Identify upselling and cross-selling opportunities within existing accounts to maximize revenue generation.Stay updated on industry trends, market conditions, and competitor activities to proactively identify potential threats and opportunities.Prepare and present reports on account performance, sales forecasts, and market insights to internal stakeholders.Increase the visibility and awareness of our company's pharmaceutical and medical products and maximize sales growth.How to apply:If you are interested in this position and believe you have the right qualifications, please send your English CV to ******.

If you have any further questions about the position, please contact us.#J-18808-Ljbffr

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada8 de febr.

Created in 2005 by the Generalitat de Catalunya (Government of Catalonia) and the University of Barcelona, IRB Barcelona is a Severo Ochoa Centre of Excellence—a seal that was awarded in 2011.

The institute is devoted to conducting research of excellence in biomedicine and to transferring results to clinical practice, thus improving people's quality of life, while simultaneously promoting the training of outstanding researchers, technology transfer, and public communication of science.

Its 29 laboratories and seven core facilities address basic questions in biology and are orientated to diseases such as cancer, metastasis, Alzheimer's, diabetes, and rare conditions.

IRB Barcelona is an international centre that hosts 500 members and 45 nationalities.

It is located in the Barcelona Science Park.

IRB Barcelona forms part of the Barcelona Institute of Science and Technology (BIST) and the "Xarxa de Centres de Recerca de Catalunya" (CERCA).

IRB Barcelona is offering a Postdoctoral Position for a young scientist from the national and international community who wishes to join the lab of Dr. Stefanie Wculek (link). We aim to recruit experienced wet-lab biologists who are curiosity-driven and responsible team players that are leading their research together with the PI.

S/he will work on projects to investigate how innate immune cells (macrophages and/or dendritic cells) adapt to different tissues, including changes in their immunometabolism.

Details of the project will be defined together with the successful candidates, based on his/her interests.

We provide a stimulating, interactive, challenging and equal opportunity team-working environment in a modern research institute, with innovative research infrastructures and core facilities.

Moreover, we offer training in hard and soft skills with world-class support at the group- and institute-level to maximize professional career development.

The position is financed by the ERC Starting Grant project "Studying the metabolism and function of myeloid dendritic cells and neutrophils in distinct tissues in health and aging (MyTissue)".

DUTIES: Lead and organize projects within the group's scientific scope with the PI.Conduct high quality research in collaboration with other team members.Participate and report results in group meetings and scientific discussions.Engage in training of junior scientists of the research group.Write manuscripts together with the PI.EXPERIENCE, KNOWLEDGE, SKILLS: Must Have – Required Education: PhD in biomedicine or biosciences (ideally completed within no more than 2 years).

Performing and disseminating of scientific studies.Skills:Highly motivated and collaborative, with enthusiasm to lead conceptually and technically challenging research projects.Fluency in written and spoken English.Organized, responsible and creative.Desirable Experience: Research on innate immune cells and/or cellular metabolism.

Supervision of students or technicians.

Coordination of collaborative research efforts.Knowledge: Flow Cytometry and sorting, Mouse models, Primary human tissue and cell culture, Bioinformatics tools for analysis of gene expression, Molecular biology techniques including cloning and CRISPR.WORKING CONDITIONS & ENTITLEMENTS: Working conditions: Employed in compliance with Spanish legislation and regulations under a full-time contract.

Employees receive the benefits of the Spanish Social Security system covering sickness, maternity/paternity leaves and injuries at work.Estimated annual gross salary: Salary commensurate with experience and qualifications.Training and Career: Training is a way of life at IRB Barcelona.

Postdoctoral researchers joining IRB Barcelona gain access to the Institute's advanced research training and career development opportunities, all within a competitive international environment.

Courses and workshops on themes of particular interest to predocs are offered regularly by the Institute.International environment: Nearly 90 Postdoctoral researchers (more than a half non-Spanish nationals) are currently working at IRB Barcelona.

Opportunity to join a prestigious, diverse and inclusive international research institution.HOW TO APPLY & SELECTION PROCESS: Applications for the above opening should include Full CV (including list of submitted publications) and Motivation letter and contact information for former supervisors. Deadline for applications: 28/02/2025.

If no suitable candidate is found, the deadline will be extended.

Early application is highly encouraged.Number of positions available: 1Selection process:Pre-selection: Will be based on CV, grades, motivation letter, experience.Interviews: Short-listed candidates will be interviewed.Job Offer: Will be sent to the successful candidate after the interview.For more information please visit our website at: www.irbbarcelona.org Note: The strengths and weaknesses of the applications will be provided upon request. If you, as an applicant, have any suggestion or wish to make a complaint regarding the selection process, please contact us at the following email address: ******.

You will receive a response within a month.

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• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada6 de febr.

Position Overview

We are seeking an innovative and experienced R&D Manager to lead the development and delivery of cutting-edge medical device solutions. The successful candidate will bring deep technical expertise, strategic leadership, and a proven track record in project and team management within the medical device industry. This role involves driving projects from concept to mass production, ensuring compliance with regulatory standards, and fostering a culture of technical excellence.

Key Responsibilities

• Lead the design, development, and delivery of innovative vascular medical device solutions.
• Oversee program management activities, including design verification, FDA submissions, and clinical trial approvals for EU and other markets.
• Manage cross-functional R&D teams, including technology SMEs specializing in materials, electronics, fluid dynamics, and more.
• Develop team members by fostering a culture of innovation, first-principle engineering, and technical expertise.
• Budget & Stakeholder Management, ensuring resource allocation aligns with strategic objectives.
• Communicate progress and technical risks to senior leadership and the board of directors.
• Translate customer needs and strategic marketing inputs into technical specifications and performance goals.
• Conduct technical design reviews and manage risks to ensure the reliability and performance of devices.
• Collaborate in preclinical and clinical trial preparation, ensuring compliance with ethics and regulatory authorities.
• Manage vendors for critical components, ensuring quality and alignment with technical requirements.
• Collaborate with marketing, clinical, and regulatory teams to drive successful outcomes.

Qualifications

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or a related field. A Master’s Degree or PhD in a similar field will be a plus.
• Extensive experience in the medical device industry, with progressive responsibilities in R&D and technical leadership.
• Expertise in catheter-based systems, medical devices for vascular therapies, or similar technologies.
• Proven experience managing cross-functional teams and large-scale project budgets.
• Deep knowledge of regulatory pathways for different markets, specially the EU.
• Strong technical skills in materials (e.g., Nitinol), testing methods, and preclinical development.
• Expertise in the industrialization of prototypes.

Key Skills

• Leadership: Proven ability to lead and develop high-performing technical teams.
• Technical Expertise: In-depth understanding of material sciences, product development, and device testing.
• Communication: Strong verbal and written communication skills for cross-functional and executive-level reporting.
• Problem-Solving: Skilled in risk assessment and mitigation in highly complex, regulated environments.
• Innovation: Commitment to fostering a culture of innovation and knowledge leadership.

What We Offer

• Opportunity to lead groundbreaking projects in the medical device industry.
• Collaborative and innovation-driven work environment.
• Comprehensive benefits and opportunities for professional development.

This role is pivotal in driving the next generation of medical device innovations. If you are passionate about transforming healthcare and have the expertise to lead from the front, we would love to hear from you!