Clinical Research Associate Ii

1 semana atrás

Lisboa, Portugal PSI CRO Tempo inteiro

**Company Description**
PSI is a leading Contract Research Organization with almost 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

- Conduct and report SSV, SIV, RMV, COV onsite monitoring visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and particiapte on audits and inspections

**Qualifications**
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- At least 2 years of independent on-site monitoring experience in Portugal
- Experience in all types of monitoring visits in Phase II and/or III
- Therapeutic area experience in Oncology /Hematology /Gastroenterology (IBD) /Infectious Diseases /Neurology is a plus
- Full working proficiency in English and Portugeese
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel

**Additional Information**
What We Offer:

- Stability, long-term cooperation
- Permanent contract, full-time job
- Hybrid or home-based work setting
- Competitive salary and benefit package
- Career development
- Unique combination of team collaboration and independent work
- Friendly and supportive colleagues
- Onboarding courses about clinical research industry
- Mentoring and on-the job training
- Comfortable and well-established modern office

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

  • Clinical Research Associate II

    Há 2 dias

    Lisboa, Portugal PSI CRO Tempo inteiro

    Company Description PSI is a leading Contract Research Organization with almost 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate II at PSI you...

  • Clinical Research Associate

    2 semanas atrás

    Lisboa, Portugal CTI Clinical Trial Services, Inc Tempo inteiro

    **Clinical Research Associate for our Lisbon office (level dependent upon experience)** **Job Purpose/Summary** As a CRA you will be responsible for the successful conduct of clinical trials and serve as main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Conduct evaluation, initiation, monitoring...

  • Clinical Associate Ii

    1 semana atrás

    Lisboa, Portugal Labcorp Tempo inteiro

    **Clinical Research Associate 2 / CRA 2 - Clinical Operations Team**: **Location: Portugal**: **A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas -...

  • Clinical Research Associate

    Há 4 dias

    Lisboa, Portugal IQVIA Tempo inteiro

    Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

  • Clinical Research Associate

    1 semana atrás

    Lisboa, Portugal TFS HealthScience Tempo inteiro

    Overview: TFS HealthScience is excited to be expanding our **Strategic Resourcing Solutions (SRS) **team and we are looking for an experienced, highly motivated **Clinical Research Associate** who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry...

  • Cra Ii

    1 dia atrás

    Lisboa, Portugal ICON Plc Tempo inteiro

    CRA Portugal ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and...

  • Clinical Research Associate

    2 semanas atrás

    Lisboa, Lisboa, Portugal IQVIA Tempo inteiro

    Clinical Research Associate Your responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

  • Clinical Research Associate Ii

    Há 3 dias

    Lisboa, Portugal Labcorp Tempo inteiro

    Labcorp Drug Development has an exciting opportunity for CRA II to work full-time, home-based or office - based in Portugal. You will be fully dedicated to one sponsor working in multiple TAs, with a focus on a variety of therapy areas like Oncology or Cardiovascular. This opportunity sits within our FSP business model - a very attractive environment with...

  • Clinical Research Associate 2

    Há 4 dias

    Lisboa, Portugal IQVIA Tempo inteiro

    Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

  • Study Start Up Associate Ii

    2 semanas atrás

    Lisboa, Portugal ICON Tempo inteiro

    Study Start Up Associate II At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...