CRA2

Iqvia

·

3 days ago

Apply
Location
Porto Salvo, Portugal
Workplace
Onsite
Type
Full-time
Source
Workday

Description

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 Harmonization guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  • Collaborating with experts at study sites and with client representatives


Qualifications:

  • University degree in scientific discipline or health care
  • 2-4 years of independent on-site monitoring experience.
  • Very good computer skills including MS Office
  • Excellent command of Portuguese and English language.
  • Organizational, time management and problem-solving skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Flexibility to travel
  • Driver’s license class B

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Excellent working environment in a stabile, international, reputable company
  • Company car, mobile phone and attractive benefits package

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Languages

Portuguese

Similar Jobs

9

CRA2

Thermofisher·China - Sichuan - Chengdu - Remote·Remote

1w ago

CRA2 - Argentina

Iqvia·Buenos Aires, Buenos Aires F.D.·Onsite

1mo ago

CRA2 (Freelancer)

Iqvia·Illkirch-Graffenstaden, Grand Est·Onsite

1y+ ago

CTA2

Iqvia·Chengdu, Sichuan

Today

Sr Clinical Research Associate II (SCRA2), FSP - Sydney or Melbourne

Fortrea·Melbourne, Victoria +1·Hybrid

1d ago

SCFP-CUPE - Winter 2027 - TA - CRM2715 B00

Uottawa·Canada

3d ago

SCFP-CUPE - Winter 2027 - Corrector - CRM2310 B00

Uottawa·Canada

3d ago

SCFP-CUPE - Winter 2027 - TA - CRM2310 B00

Uottawa·Canada

3d ago

SCFP-CUPE - Winter 2027 - TA - CRM2715 A00

Uottawa·Canada

3d ago