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Open roles

· Clinical-Research-Associate

Experienced Clinical Research Associate FSP Romania

IQVIA

2+ yrsRemote · EuropeFull TimeListed 5d ago
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About the role

structured by ORI

Experienced Clinical Research Associate - Sponsor Dedicated IQVIA Romania is looking for talented and motivated team member to join our Sponsor dedicated team as Senior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide…

What you will do

  • 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

What they are looking for

  • University degree in scientific discipline or health care
  • Experience in Pharma Industry, and/or Clinical Trials environment performing independent monitoring for at least 2 years.
  • Very good computer skills including MS Office
  • Excellent command of Romanian and English language. Romania based.
  • 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

Benefits

  • Company car/Car Allowance
  • mobile phone
  • attractive benefits packaging
Good Clinical PracticeInternational Conference on Harmonization guidelinesmonitoringorganizational skillstime managementproblem-solvingMS Office
Full posting text

Experienced Clinical Research Associate - Sponsor Dedicated

IQVIA Romania is looking for talented and motivated team member to join our Sponsor dedicated team as Senior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

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

Your Profile

University degree in scientific discipline or health care

Experience in Pharma Industry, and/or Clinical Trials environment performing independent monitoring for at least 2 years.

Very good computer skills including MS Office

Excellent command of Romanian and English language. Romania based.

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/Car Allowance, mobile phone and attractive benefits packaging

Home-based role on any part of the country.

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

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.

Originally posted on Himalayas

Clinical-Research-AssociateClinical-MonitoringClinical-TrialsDrug-DevelopmentPharmaceutical-ResearchClinical-Research-SpecialistClinical-Research-Associate-II
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Opportunity details

Deadline
Closing in 24d · 29 Oct

As stated by the source. Anything not shown was not stated.

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