Senior Clinical Research Associate, Sponsor dedicated in Poland at IQVIA
zdalnie, województwo śląskie, Poland -
Full Time


Start Date

Immediate

Expiry Date

01 Aug, 25

Salary

0.0

Posted On

02 May, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Trials, Life Science, Training, Regulatory Requirements, Harmonization, Communication Skills

Industry

Pharmaceuticals

Description

Are you interested in collaborating with leading pharma companies to help patients all around the world?
When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, 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 health care
  • Minimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
  • Strong experience in monitoring of clinical trials
  • 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
  • Good command of Polish and English language
  • Flexibility to travel
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)
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