Senior Clinical Research Associate (m/f/d), Single Sponsor, home-based Aust at IQVIA
Home Office, Tirol, Austria -
Full Time


Start Date

Immediate

Expiry Date

02 Aug, 25

Salary

0.0

Posted On

02 May, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulatory Requirements, Harmonization, Life Science, Communication Skills, English, German

Industry

Pharmaceuticals

Description

Join IQVIA as a Sr CRA (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you’re just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll 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.

QUALIFICATIONS:

  • University Degree in life science or other scientific discipline or apprenticeship in the health care field
  • Minimum of two years of on-site monitoring experience
  • Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
  • Fluency in German on at least C1 level and a good command of English
  • Flexibility to travel up to 40-60% of working time
  • Driver’s license class B
Responsibilities
  • 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 (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives
  • Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
  • Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included
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