Junior Clinical Research Associate

1 semana atrás

Lisboa, Lisboa, Portugal Novo Nordisk Tempo inteiro
The Position

As a Junior Clinical Research Associate (CRA), you'll be a crucial member in managing and overseeing clinical trials in alignment with established protocols, regulatory guidelines, and company standards. You'll have a significant role in advancing our mission to introduce groundbreaking treatments to patients.

Key Responsibilities:
  • Conduct site selection, initiation, monitoring, and close-out visits.
  • Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Monitor patient safety and data quality throughout the trial.
  • Collaborate with investigators and site staff to ensure smooth trial operations.
  • Prepare and review study-related documentation and reports.
Qualifications

Having an educational background in Life Sciences is a must. Additional post graduations in Clinical Research will be an advantage.

To excel in this role, you should possess:

  • Previous experience in Clinical Research as a CRA, Study Coordinator, or CTA (including CROs).
  • Good knowledge of clinical research processes, regulations, and guidelines in the Portuguese environment.
  • Excellent organizational and communication skills.
  • Ability to work independently and collaboratively in a team.
  • Attention to detail and ability to manage multiple tasks simultaneously.
  • Proficiency in English and Portuguese.

The ideal candidate should be based in either Lisbon or Porto and be willing to travel frequently to visit trial sites. A driving license is required.

About the Department

In the Clinical Medical and Regulatory (CMR) department, we strive to combat severe chronic diseases.

In Clinical, our focus is on delivering high-standard clinical outcomes to aid in the development of innovative medicines. Our promising pipeline reflects a significant increase in R&D investment in Portugal from 2020 to 2023.

In Medical Affairs, we merge business with science and engage with Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs) to enhance care for individuals with chronic conditions.

Lastly, in Regulatory, we ensure our compliance and the provision of top-quality medications to those in need.

Working at Novo Nordisk

Novo Nordisk is a distinguished global healthcare organization with a century-long legacy of battling serious chronic ailments. Expanding beyond diabetes, we are substantially growing our reach, impacting millions globally and touching over 40 million lives daily. These achievements have positioned us among the top 20 most valuable companies globally by market cap. Our success is underpinned by the collective expertise and collaboration of our 63,000+ employees worldwide. We value the unique skills and perspectives our team members bring and actively nurture their potential. At Novo Nordisk, we are working toward a greater cause. Join us and let's change lives together.

Contact

To apply, please visit our careers page; we do not accept direct CV submissions.

Deadline

Application deadline: 30th of May 2024

We are committed to fostering an inclusive recruitment process and providing equal opportunities to all applicants.

Novo Nordisk acknowledges that merely aiming to be the best company is inadequate. Our objective is to be the finest company for the world, and this can only be achieved through a diverse workforce with varied perspectives, backgrounds, and cultures. We are dedicated to cultivating an inclusive environment that celebrates our employees' diversity, the patients we serve, and the communities we impact. Together, we make a difference.

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