Cra / scra
The pace and scale of change today is staggering
The world changes rapidly, at a very fast pace. But one thing remains the same at Pivotal, our commitment with medical science while using technology, to make a positive impact.
We need more than ever to onboard the best talent: people with solid insights, experience, commitment and attitude to become a trusted guide for our clients; people striving to always give the best; people with resilience.
In return, we will provide you with an exceptional experience, you will receive permanent mentoring and training and a push to always take one step further as well as untold international experience that will help you grow and will accompany all your life.
Explore careers at Pivotal and join us in building a better working world.
Building a better
working world
Working at Pivotal
At Pivotal we deliver impact through innovation. This is our DNA and how we approach our workWe want our clients´ to succeed and this requires deep medical and data science knowledge. So, we hire people with diverse skills and backgrounds, that can flatten our clients´ research and their way to success. This sounds like a huge challenge, but the restless efforts of each individual at Pivotal will get us there. With a culture of team and mentoring, we are committed in building a better working place. We will talk about every next step of your career to take you to a place that better matches your curiosity and ambition. Whether you are new to the profession, an executive, an experienced professional or a university student, and medical research, while using technology as well as contributing to a better clinical research world which is appealing to you, we invite you to explore careers at Pivotal.
Extraordinary Careers
Want to embrace new challenges every day? Seduced to join a motivated team? Our exceptional people are helping to build a better clinical research world.What I love about Pivotal is how the culture has grown to embrace a greater diversity of perspectives and the creation of an agile working environment.
Alejandra Bayano, Project Director
All of the graduates I started with come together as one group, we formed a camaraderie right from the beginning. Many people I keep contact with, some are great friends and we have followed each other’s careers.
Marta Vazquez, Senior Project Manager
An experience for a life
No matter how long you remain with us, we value the exchange of perspectives and experiences while you are part of Pivotal. Our relationship will last a lifetime.Deliver impact through innovation
We are in constant search of trends, methodologies and tools and we apply them to our work. We foster an agile culture and look for people to help us write the steps needed to advance clinical research.The role I have now is about strengthening our data driven culture to make a better clinical research world. We have deployed an DevOps agile culture to navigate through unexpected changes without compromising product quality, patients’ safety and data integrity.
Jose Lisbona, Director Software Architecture
Job opportunities
AllCRA/SCRA
Italy - 05/02/2025Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.
Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct experience with our clients and offer career growth and professional development within a scientific and data driven company. You’ll have the opportunity to put your passion to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Why Pivotal
- We are passionate and fully committed with medical science while using technology, to make a positive impact
- We provide an exceptional experience. We take care of our employees and we ensure everyone receives permanent mentoring and training and a push to always take one step further as well as untold international experience that will help you grow and will accompany all your life
- We are continuously building the company, bringing together diversity of thoughts, backgrounds, cultures, and perspectives being able to create a place where everyone feels like they belong
Your responsibilities will include
:- Be part of multi-national project teams and focus on delivering exemplary levels of customer service on multiple, challenging studies
- Perform site selection, initiation, monitoring and close-out visits
- Collaborate with the Regulatory team to obtain Ethic Committees (ECs) and Health Authorities (HAs) approvals in accordance with national/international regulations
- Evaluate the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines and local regulations. Use judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans
- Manage site progress by tracking recruitment, eCRF completion, and data query resolution
- Participate in problem-solving and risk-mitigation strategies
- Collaborate with experts at study sites and with client representatives
- Maintain a working knowledge of relevant regulations and company SOPs/processes
- Demonstrate diligence in protecting the confidentiality of each subject/patient
- Maintain study files in collaboration with our CTAs and eTMF specialists.
Requirements:
- University Degree in life science or other scientific discipline or apprenticeship in health care
- Minimum of two years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
- Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Flexibility to travel 6-8 visits per month
Skills
:
- Demonstrated problem-solving skills, a strong sense of urgency, keen attention to detail, and the ability to plan, organize and successfully execute in an environment under time and resource pressures
- Strong written and verbal communication skills, attention to detail and ability to work in a fast-pace environment
- Ability to work autonomously
- Fluency in Italian and English
- Good knowledge of Office (Word, Excel and PowerPoint)
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Trainings to help you build your therapeutic knowledge
- Dynamic work environments that expose you to new experiences
Commitment to Equal Opportunity:
At Pivotal, we believe that diversity and inclusion are essential to the success of our team. We are committed to providing equal employment opportunities to all candidates, regardless of race, gender, sexual orientation, disability, or any other characteristic.CRA/SCRA
Italy - 05/02/2025Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.
Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct experience with our clients and offer career growth and professional development within a scientific and data driven company. You’ll have the opportunity to put your passion to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Why Pivotal
- We are passionate and fully committed with medical science while using technology, to make a positive impact
- We provide an exceptional experience. We take care of our employees and we ensure everyone receives permanent mentoring and training and a push to always take one step further as well as untold international experience that will help you grow and will accompany all your life
- We are continuously building the company, bringing together diversity of thoughts, backgrounds, cultures, and perspectives being able to create a place where everyone feels like they belong
Your responsibilities will include
:- Be part of multi-national project teams and focus on delivering exemplary levels of customer service on multiple, challenging studies
- Perform site selection, initiation, monitoring and close-out visits
- Collaborate with the Regulatory team to obtain Ethic Committees (ECs) and Health Authorities (HAs) approvals in accordance with national/international regulations
- Evaluate the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines and local regulations. Use judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans
- Manage site progress by tracking recruitment, eCRF completion, and data query resolution
- Participate in problem-solving and risk-mitigation strategies
- Collaborate with experts at study sites and with client representatives
- Maintain a working knowledge of relevant regulations and company SOPs/processes
- Demonstrate diligence in protecting the confidentiality of
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